Variant report

Variant	esv3438651
Chromosome Location	chr16:31373520-31422007
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:731)
CpG islands
(count:1221)
Chromatin interactive
region (count:42)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:731 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:31393918-31394149	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:31383068-31383352	HepG2	liver:	n/a	n/a
3	ATF1	chr16:31397640-31398214	K562	blood:	n/a	n/a
4	ATF2	chr16:31376334-31376899	GM12878	blood:	n/a	n/a
5	BATF	chr16:31378233-31378510	GM12878	blood:	n/a	n/a
6	BHLHE40	chr16:31393969-31394197	K562	blood:	n/a	n/a
7	BHLHE40	chr16:31405046-31405194	K562	blood:	n/a	chr16:31405138-31405159 chr16:31405145-31405154
8	BHLHE40	chr16:31382864-31383366	HepG2	liver:	n/a	n/a
9	BHLHE40	chr16:31415385-31415567	K562	blood:	n/a	n/a
10	BHLHE40	chr16:31376441-31376816	GM12878	blood:	n/a	n/a
11	BHLHE40	chr16:31415813-31416015	K562	blood:	n/a	n/a
12	BHLHE40	chr16:31397666-31397921	K562	blood:	n/a	n/a
13	BRCA1	chr16:31397692-31397836	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr16:31411149-31411357	K562	blood:	n/a	n/a
15	CBX3	chr16:31415859-31416232	K562	blood:	n/a	n/a
16	CBX3	chr16:31411108-31411433	K562	blood:	n/a	n/a
17	CEBPB	chr16:31393856-31394238	HepG2	liver:	n/a	chr16:31394038-31394049
18	CEBPB	chr16:31418803-31418933	HepG2	liver:	n/a	chr16:31418843-31418854
19	CEBPB	chr16:31393861-31394163	ECC-1	luminal epithelium:	n/a	chr16:31394038-31394049
20	CEBPB	chr16:31387851-31387930	Hela-S3	cervix:	n/a	chr16:31387896-31387907
21	CEBPB	chr16:31397658-31397941	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr16:31383080-31383500	HepG2	liver:	n/a	chr16:31383330-31383341 chr16:31383331-31383342 chr16:31383330-31383343
23	CEBPB	chr16:31393857-31394226	A549	lung:	n/a	chr16:31394038-31394049
24	CEBPB	chr16:31375536-31375857	A549	lung:	n/a	chr16:31375698-31375709
25	CEBPB	chr16:31393906-31394181	K562	blood:	n/a	chr16:31394038-31394049
26	CEBPB	chr16:31383200-31383418	K562	blood:	n/a	chr16:31383330-31383341 chr16:31383331-31383342 chr16:31383330-31383343
27	CEBPB	chr16:31397643-31398254	A549	lung:	n/a	n/a
28	CEBPB	chr16:31375540-31375818	K562	blood:	n/a	chr16:31375698-31375709
29	CEBPB	chr16:31393741-31394339	A549	lung:	n/a	chr16:31394038-31394049
30	CEBPB	chr16:31387778-31388040	A549	lung:	n/a	chr16:31387896-31387907
31	CEBPB	chr16:31375546-31375881	H1-hESC	embryonic stem cell:	n/a	chr16:31375698-31375709
32	CEBPB	chr16:31393848-31394132	HepG2	liver:	n/a	chr16:31394038-31394049
33	CEBPB	chr16:31393844-31394250	A549	lung:	n/a	chr16:31394038-31394049
34	CEBPB	chr16:31393856-31394222	IMR90	lung:	n/a	chr16:31394038-31394049
35	CEBPB	chr16:31397647-31398188	IMR90	lung:	n/a	n/a
36	CEBPB	chr16:31414054-31414279	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr16:31375527-31375818	HepG2	liver:	n/a	chr16:31375698-31375709
38	CEBPB	chr16:31393857-31394235	Hela-S3	cervix:	n/a	chr16:31394038-31394049
39	CEBPB	chr16:31387817-31388038	IMR90	lung:	n/a	chr16:31387896-31387907
40	CEBPB	chr16:31393836-31394245	K562	blood:	n/a	chr16:31394038-31394049
41	CEBPB	chr16:31387881-31387917	H1-hESC	embryonic stem cell:	n/a	chr16:31387896-31387907
42	CEBPB	chr16:31375551-31375735	Hela-S3	cervix:	n/a	chr16:31375698-31375709
43	CEBPB	chr16:31397767-31398238	K562	blood:	n/a	n/a
44	CEBPB	chr16:31393926-31394110	HepG2	liver:	n/a	chr16:31394038-31394049
45	CEBPB	chr16:31393799-31394221	MCF-7	breast:	n/a	chr16:31394038-31394049
46	CEBPB	chr16:31392600-31392672	HepG2	liver:	n/a	n/a
47	CEBPB	chr16:31393853-31394237	H1-hESC	embryonic stem cell:	n/a	chr16:31394038-31394049
48	CEBPB	chr16:31383138-31383532	HepG2	liver:	n/a	chr16:31383330-31383341 chr16:31383331-31383342 chr16:31383330-31383343
49	CEBPB	chr16:31387819-31388048	HepG2	liver:	n/a	chr16:31387896-31387907
50	CEBPB	chr16:31381034-31381328	K562	blood:	n/a	chr16:31381051-31381063 chr16:31381162-31381173

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:31383136-31383186	CMK	blood:	n/a
2	chr16:31383136-31383186	CMK	blood:	n/a
3	chr16:31408712-31408762	NHDF-neo	bronchial:	n/a
4	chr16:31383689-31383739	CMK	blood:	n/a
5	chr16:31408900-31408950	HCT-116	colon:	n/a
6	chr16:31383800-31383850	HMEC	breast:	n/a
7	chr16:31383642-31383692	BJ	skin:	n/a
8	chr16:31408900-31408950	T-47D	breast:	n/a
9	chr16:31408900-31408950	HRCEpiC	kidney:	n/a
10	chr16:31382930-31382980	RPTEC	kidney:	n/a
11	chr16:31383049-31383099	HPAEpiC	pulmonary alveolar:	n/a
12	chr16:31404385-31404435	NB4	blood:	n/a
13	chr16:31383049-31383099	NT2-D1	testis:	n/a
14	chr16:31385282-31385332	GM12892	blood:	n/a
15	chr16:31404385-31404435	PrEC	prostate:	n/a
16	chr16:31415135-31415185	PANC-1	pancreas:	n/a
17	chr16:31408898-31408948	CMK	blood:	n/a
18	chr16:31383689-31383739	Hepatocyte	liver:	n/a
19	chr16:31384854-31384904	K562	blood:	n/a
20	chr16:31405101-31405151	PFSK-1	brain:	n/a
21	chr16:31403683-31403733	ECC-1	luminal epithelium:	n/a
22	chr16:31383049-31383099	T-47D	breast:	n/a
23	chr16:31405101-31405151	H1-hESC	embryonic stem cell:	embryo
24	chr16:31405101-31405151	PrEC	prostate:	n/a
25	chr16:31382930-31382980	NHDF-neo	bronchial:	n/a
26	chr16:31379850-31379900	HCF	heart:	n/a
27	chr16:31405101-31405151	ovcar-3	ovarian:	n/a
28	chr16:31394096-31394146	SK-N-MC	brain:	n/a
29	chr16:31383800-31383850	SK-N-SH	brain:	n/a
30	chr16:31383689-31383739	PANC-1	pancreas:	n/a
31	chr16:31394096-31394146	SK-N-SH	brain:	n/a
32	chr16:31408712-31408762	HRCEpiC	kidney:	n/a
33	chr16:31408712-31408762	SK-N-SH_RA	brain:	n/a
34	chr16:31383049-31383099	A549	lung:	n/a
35	chr16:31385282-31385332	HRE	kidney:	n/a
36	chr16:31408867-31408917	BJ	skin:	n/a
37	chr16:31383689-31383739	AG10803	skin:	n/a
38	chr16:31383055-31383105	A549	lung:	n/a
39	chr16:31405101-31405151	GM12878	blood:	n/a
40	chr16:31403683-31403733	U87	brain:	n/a
41	chr16:31383800-31383850	Caco-2	colon:	n/a
42	chr16:31380955-31381005	GM12891	blood:	n/a
43	chr16:31394096-31394146	AoSMC	blood vessel:	n/a
44	chr16:31384854-31384904	NHBE	bronchial:	n/a
45	chr16:31383689-31383739	HRPEpiC	eye:	n/a
46	chr16:31379850-31379900	SAEC	small airway:	n/a
47	chr16:31382930-31382980	BE2_C	brain:	n/a
48	chr16:31415135-31415185	GM12892	blood:	n/a
49	chr16:31383689-31383739	Caco-2	colon:	n/a
50	chr16:31383055-31383105	LNCaP	prostate:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:31210088..31212340-chr16:31394934..31396968,2	MCF-7	breast:
2	chr16:31393820..31395534-chr16:31395638..31397833,2	MCF-7	breast:
3	chr16:31403402..31405876-chr16:31406306..31408936,2	MCF-7	breast:
4	chr16:31408712..31410722-chr16:31883758..31886436,2	K562	blood:
5	chr16:31384535..31387271-chr16:31390776..31392528,2	K562	blood:
6	chr16:31277354..31279123-chr16:31386199..31389124,2	K562	blood:
7	chr16:31418569..31421375-chr16:31470811..31472382,2	K562	blood:
8	chr16:30996013..30996554-chr16:31393734..31394639,2	MCF-7	breast:
9	chr16:31393820..31395534-chr16:31395638..31397833,2	MCF-7	breast:
10	chr16:31400836..31402888-chr16:31406431..31408279,2	MCF-7	breast:
11	chr16:31396941..31397680-chr16:31454467..31454971,2	MCF-7	breast:
12	chr16:31383533..31386035-chr16:31390623..31392276,2	K562	blood:
13	chr16:31404071..31406519-chr16:31413482..31415617,2	K562	blood:
14	chr16:31365891..31370863-chr16:31373415..31376025,5	K562	blood:
15	chr16:31373565..31374565-chr20:49341478..49342019,2	MCF-7	breast:
16	chr16:31409305..31411632-chr16:31412830..31415079,2	K562	blood:
17	chr16:31383533..31386035-chr16:31390623..31392276,2	K562	blood:
18	chr16:31397034..31399746-chr16:31400566..31403518,3	MCF-7	breast:
19	chr16:31421440..31423160-chr16:31426005..31428046,2	MCF-7	breast:
20	chr16:31370070..31372965-chr16:31413920..31417255,3	K562	blood:
21	chr16:31397034..31399746-chr16:31400566..31403518,3	MCF-7	breast:
22	chr16:31396502..31398458-chr16:31424571..31427313,2	K562	blood:
23	chr16:31415190..31417211-chr16:31469405..31471164,2	K562	blood:
24	chr16:31400836..31402888-chr16:31406431..31408279,2	MCF-7	breast:
25	chr16:31191136..31192870-chr16:31404226..31406023,2	MCF-7	breast:
26	chr16:31375617..31378307-chr16:31436876..31438549,2	K562	blood:
27	chr16:31415289..31417265-chr16:31468628..31470943,2	MCF-7	breast:
28	chr16:31375595..31378224-chr16:31462241..31464094,2	K562	blood:
29	chr16:31189640..31192983-chr16:31385615..31388783,3	MCF-7	breast:
30	chr16:31418631..31421528-chr16:31427897..31429526,2	MCF-7	breast:
31	chr16:31414435..31419605-chr16:31467873..31472757,5	K562	blood:
32	chr16:31083852..31086357-chr16:31391531..31394132,2	MCF-7	breast:
33	chr11:9482374..9482990-chr16:31415165..31415976,2	Hela-S3	cervix:
34	chr16:31404071..31406519-chr16:31413482..31415617,2	K562	blood:
35	chr16:31384535..31387271-chr16:31390776..31392528,2	K562	blood:
36	chr16:31383689..31387249-chr16:31389640..31393278,4	MCF-7	breast:
37	chr16:31190461..31193356-chr16:31392398..31395523,4	MCF-7	breast:
38	chr16:31370114..31372263-chr16:31373641..31375780,2	MCF-7	breast:
39	chr16:31405158..31408011-chr16:31425171..31426679,2	MCF-7	breast:
40	chr16:31190410..31192948-chr16:31385235..31387421,2	MCF-7	breast:
41	chr16:31407031..31409416-chr16:31465348..31468192,2	MCF-7	breast:
42	chr16:31383689..31387249-chr16:31389640..31393278,4	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ITGAX-1	chr16:31413886-31414189	ENSG00000260757.1
2	lnc-ITGAX-1	chr16:31414558-31416020	ENSG00000260757.1

No data

Variant related genes	Relation type
ENSG00000261245	TF binding region
ITGAX	TF binding region
ENSG00000260757	TF binding region
ITGAD	TF binding region
ENSG00000261245	CpG island
ITGAX	CpG island
ENSG00000260757	CpG island
ITGAD	CpG island
ENSG00000099377	chromatin interactions
ENSG00000140678	chromatin interactions
ENSG00000185947	chromatin interactions
ENSG00000140691	chromatin interactions
ENSG00000156886	chromatin interactions
ENSG00000167394	chromatin interactions
ENSG00000260757	chromatin interactions
ENSG00000089280	chromatin interactions
ENSG00000260267	chromatin interactions
ENSG00000167395	chromatin interactions
ENSG00000166478	chromatin interactions
ENSG00000252876	chromatin interactions

Extended variants
information (count: 2050 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:2050 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184225456	chr16:31373546-31373547	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs200734472	chr16:31373564-31373565	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs377459367	chr16:31373574-31373575	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs116039611	chr16:31373587-31373588	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs546424845	chr16:31373644-31373645	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs60020095	chr16:31373682-31373683	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs397967107	chr16:31373684-31373685	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs571200176	chr16:31373831-31373832	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs563111756	chr16:31373871-31373872	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs201823564	chr16:31373874-31373875	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs371153209	chr16:31373924-31373925	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs199816923	chr16:31373936-31373937	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs74413955	chr16:31373942-31373943	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs534569493	chr16:31373960-31373961	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs199910375	chr16:31373985-31373986	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs150562711	chr16:31373986-31373987	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs201384441	chr16:31373991-31373992	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs554674355	chr16:31374006-31374007	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs200497327	chr16:31374010-31374011	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs376618435	chr16:31374012-31374013	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs139553693	chr16:31374025-31374026	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs559233176	chr16:31374057-31374058	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs577520206	chr16:31374065-31374066	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs538117251	chr16:31374120-31374121	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs556834032	chr16:31374178-31374179	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs574714214	chr16:31374206-31374207	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs201732371	chr16:31374218-31374219	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs75318258	chr16:31374256-31374257	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs147426364	chr16:31374258-31374259	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs139483955	chr16:31374276-31374277	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs369932001	chr16:31374279-31374280	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs199668358	chr16:31374288-31374289	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs145025324	chr16:31374294-31374295	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs147598964	chr16:31374306-31374307	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs149061469	chr16:31374307-31374308	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs142089990	chr16:31374330-31374331	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs199963723	chr16:31374348-31374349	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs374910232	chr16:31374357-31374358	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs151306268	chr16:31374359-31374360	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs140533202	chr16:31374363-31374364	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs529634102	chr16:31374384-31374385	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs145914477	chr16:31374390-31374391	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs369310242	chr16:31374404-31374405	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs371702251	chr16:31374413-31374414	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs201179603	chr16:31374437-31374438	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs566560969	chr16:31374445-31374446	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs377119705	chr16:31374453-31374454	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs533827477	chr16:31374466-31374467	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs552313404	chr16:31374488-31374489	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs369681895	chr16:31374516-31374517	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:383 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31343000-31400800	Weak transcription	Right Atrium	heart
2	chr16:31369400-31375800	Weak transcription	Liver	Liver
3	chr16:31369600-31375200	Weak transcription	GM12878-XiMat	blood
4	chr16:31369600-31381200	Weak transcription	Spleen	Spleen
5	chr16:31369800-31377400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr16:31370000-31376400	Weak transcription	Primary B cells from peripheral blood	blood
7	chr16:31371000-31377400	Weak transcription	Lung	lung
8	chr16:31371400-31375600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr16:31371400-31378000	Weak transcription	Primary B cells from cord blood	blood
10	chr16:31372000-31374600	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr16:31372600-31374600	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr16:31372600-31375400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr16:31373000-31374200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr16:31373200-31375200	Strong transcription	Primary neutrophils fromperipheralblood	blood
15	chr16:31373400-31378200	Enhancers	Primary T cells fromperipheralblood	blood
16	chr16:31373400-31381200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr16:31374200-31374400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr16:31374600-31374800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
19	chr16:31374600-31375800	Genic enhancers	Primary monocytes fromperipheralblood	blood
20	chr16:31374600-31377600	Genic enhancers	Monocytes-CD14+_RO01746	blood
21	chr16:31375200-31375800	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr16:31375200-31375800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
23	chr16:31375200-31378200	Genic enhancers	Primary neutrophils fromperipheralblood	blood
24	chr16:31375200-31378200	Enhancers	GM12878-XiMat	blood
25	chr16:31375400-31381600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr16:31375600-31379800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr16:31375800-31377000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr16:31375800-31377200	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr16:31376400-31377000	Enhancers	Primary B cells from peripheral blood	blood
30	chr16:31377000-31378200	Weak transcription	Primary B cells from peripheral blood	blood
31	chr16:31377000-31378400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr16:31377200-31378000	Genic enhancers	Primary monocytes fromperipheralblood	blood
33	chr16:31377400-31377600	Flanking Active TSS	Lung	lung
34	chr16:31377400-31379800	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr16:31377600-31378400	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
36	chr16:31377600-31379800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr16:31377600-31384600	Weak transcription	Lung	lung
38	chr16:31377800-31379800	Enhancers	Primary hematopoietic stem cells	blood
39	chr16:31377800-31379800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr16:31378000-31380000	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr16:31378000-31381000	Enhancers	Primary B cells from cord blood	blood
42	chr16:31378200-31378800	Transcr. at gene 5' and 3'	Primary neutrophils fromperipheralblood	blood
43	chr16:31378200-31379200	Weak transcription	GM12878-XiMat	blood
44	chr16:31378200-31379600	Enhancers	Primary B cells from peripheral blood	blood
45	chr16:31378400-31379800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr16:31378800-31379000	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr16:31378800-31379800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
48	chr16:31379200-31379400	Enhancers	GM12878-XiMat	blood
49	chr16:31379400-31379600	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr16:31379600-31386400	Weak transcription	Primary B cells from peripheral blood	blood

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