Variant report

Variant	nsv516006
Chromosome Location	chr10:49707942-49723300
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:697)
CpG islands
(count:122)
Chromatin interactive
region (count:64)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:697 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:49714503-49714913	K562	blood:	n/a	n/a
2	ARID3A	chr10:49715145-49715390	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:49713702-49713754	K562	blood:	n/a	n/a
4	ARID3A	chr10:49714573-49714848	HepG2	liver:	n/a	n/a
5	BACH1	chr10:49716040-49716159	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr10:49714441-49714585	K562	blood:	n/a	n/a
7	BHLHE40	chr10:49712840-49712973	K562	blood:	n/a	n/a
8	BHLHE40	chr10:49716230-49716334	K562	blood:	n/a	n/a
9	BHLHE40	chr10:49713518-49714275	K562	blood:	n/a	chr10:49714139-49714155
10	BHLHE40	chr10:49714483-49715086	K562	blood:	n/a	n/a
11	BRCA1	chr10:49714693-49714870	HepG2	liver:	n/a	n/a
12	CBX3	chr10:49722290-49722710	K562	blood:	n/a	n/a
13	CBX3	chr10:49721057-49721457	K562	blood:	n/a	n/a
14	CBX3	chr10:49714372-49714934	K562	blood:	n/a	n/a
15	CEBPB	chr10:49714150-49714461	HepG2	liver:	n/a	chr10:49714274-49714285
16	CEBPB	chr10:49714099-49714825	K562	blood:	n/a	chr10:49714274-49714285
17	CHD2	chr10:49712908-49713023	K562	blood:	n/a	n/a
18	CHD2	chr10:49714633-49714854	K562	blood:	n/a	n/a
19	CTCF	chr10:49714680-49714830	AG04449	skin:	n/a	chr10:49714691-49714701 chr10:49714772-49714790 chr10:49714689-49714702 chr10:49714767-49714788 chr10:49714774-49714787 chr10:49714773-49714789
20	CTCF	chr10:49713600-49713750	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr10:49714377-49715094	K562	blood:	n/a	chr10:49714691-49714701 chr10:49714772-49714790 chr10:49714689-49714702 chr10:49714767-49714788 chr10:49714774-49714787 chr10:49714773-49714789
22	CTCF	chr10:49714720-49714870	GM12868	blood:	n/a	chr10:49714772-49714790 chr10:49714767-49714788 chr10:49714774-49714787 chr10:49714773-49714789
23	CTCF	chr10:49714640-49714790	GM12874	blood:	n/a	chr10:49714691-49714701 chr10:49714772-49714790 chr10:49714689-49714702 chr10:49714767-49714788 chr10:49714774-49714787 chr10:49714773-49714789
24	CTCF	chr10:49718120-49718270	MCF-7	breast:	n/a	n/a
25	CTCF	chr10:49718120-49718270	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr10:49713584-49713685	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr10:49718120-49718270	NHLF	lung:	n/a	n/a
28	CTCF	chr10:49718052-49718305	MCF-7	breast:	n/a	n/a
29	CTCF	chr10:49713612-49713687	GM19240	blood:	n/a	n/a
30	CTCF	chr10:49717978-49718370	K562	blood:	n/a	n/a
31	CTCF	chr10:49718060-49718210	HCT-116	colon:	n/a	n/a
32	CTCF	chr10:49713620-49713770	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr10:49714600-49714750	HA-sp	spinal cord:	n/a	chr10:49714691-49714701 chr10:49714689-49714702
34	CTCF	chr10:49718174-49718237	ProgFib	skin:	n/a	n/a
35	CTCF	chr10:49714660-49714810	GM12875	blood:	n/a	chr10:49714691-49714701 chr10:49714772-49714790 chr10:49714689-49714702 chr10:49714767-49714788 chr10:49714774-49714787 chr10:49714773-49714789
36	CTCF	chr10:49714719-49714834	Pancreas_OC	pancreas:	n/a	chr10:49714772-49714790 chr10:49714767-49714788 chr10:49714774-49714787 chr10:49714773-49714789
37	CTCF	chr10:49713560-49713710	GM12874	blood:	n/a	n/a
38	CTCF	chr10:49718060-49718210	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr10:49713584-49713716	GM10248	blood:	n/a	n/a
40	CTCF	chr10:49718060-49718210	BJ	skin:	n/a	n/a
41	CTCF	chr10:49713660-49713810	NB4	blood:	n/a	n/a
42	CTCF	chr10:49718080-49718230	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr10:49718103-49718278	GM19239	blood:	n/a	n/a
44	CTCF	chr10:49714600-49714750	WERI-Rb-1	eye:	n/a	chr10:49714691-49714701 chr10:49714689-49714702
45	CTCF	chr10:49713680-49713830	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr10:49713440-49713590	GM06990	blood:	n/a	n/a
47	CTCF	chr10:49714643-49714845	Fibrobl	skin:	n/a	chr10:49714691-49714701 chr10:49714772-49714790 chr10:49714689-49714702 chr10:49714767-49714788 chr10:49714774-49714787 chr10:49714773-49714789
48	CTCF	chr10:49718120-49718270	HPF	lung:	n/a	n/a
49	CTCF	chr10:49714700-49714850	GM12870	blood:	n/a	chr10:49714772-49714790 chr10:49714767-49714788 chr10:49714774-49714787 chr10:49714773-49714789
50	CTCF	chr10:49713600-49713750	HEK293	kidney:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:49716328-49716378	IMR90	lung:	fetal
2	chr10:49716328-49716378	BE2_C	brain:	n/a
3	chr10:49716328-49716378	LNCaP	prostate:	n/a
4	chr10:49716328-49716378	AG04450	lung:	fetal
5	chr10:49710976-49711026	HNPCEpiC	eye:	n/a
6	chr10:49710976-49711026	SKMC	muscle:	n/a
7	chr10:49710976-49711026	HCF	heart:	n/a
8	chr10:49710976-49711026	HCM	heart:	n/a
9	chr10:49710976-49711026	BE2_C	brain:	n/a
10	chr10:49710976-49711026	HCT-116	colon:	n/a
11	chr10:49716328-49716378	A549	lung:	n/a
12	chr10:49710976-49711026	GM12891	blood:	n/a
13	chr10:49710976-49711026	GM12892	blood:	n/a
14	chr10:49710976-49711026	NHDF-neo	bronchial:	n/a
15	chr10:49710976-49711026	HRCEpiC	kidney:	n/a
16	chr10:49716328-49716378	Hela-S3	cervix:	n/a
17	chr10:49710976-49711026	PFSK-1	brain:	n/a
18	chr10:49716328-49716378	MCF10A-Er-Src	breast:	n/a
19	chr10:49716328-49716378	NT2-D1	testis:	n/a
20	chr10:49710976-49711026	AG04450	lung:	fetal
21	chr10:49710976-49711026	SK-N-MC	brain:	n/a
22	chr10:49716328-49716378	HNPCEpiC	eye:	n/a
23	chr10:49716328-49716378	SK-N-SH	brain:	n/a
24	chr10:49710976-49711026	K562	blood:	n/a
25	chr10:49710976-49711026	HRPEpiC	eye:	n/a
26	chr10:49716328-49716378	GM12892	blood:	n/a
27	chr10:49716328-49716378	NHDF-neo	bronchial:	n/a
28	chr10:49710976-49711026	ECC-1	luminal epithelium:	n/a
29	chr10:49710976-49711026	HRE	kidney:	n/a
30	chr10:49716328-49716378	HepG2	liver:	n/a
31	chr10:49716328-49716378	ProgFib	skin:	n/a
32	chr10:49710976-49711026	AoSMC	blood vessel:	n/a
33	chr10:49716328-49716378	HAEpiC	amniotic membrane:	n/a
34	chr10:49710976-49711026	U87	brain:	n/a
35	chr10:49710976-49711026	MCF-7	breast:	n/a
36	chr10:49710976-49711026	GM06990	blood:	n/a
37	chr10:49716328-49716378	GM06990	blood:	n/a
38	chr10:49710976-49711026	HepG2	liver:	n/a
39	chr10:49716328-49716378	BJ	skin:	n/a
40	chr10:49716328-49716378	GM12878	blood:	n/a
41	chr10:49710976-49711026	HUVEC	blood vessel:	n/a
42	chr10:49716328-49716378	Jurkat	blood:	n/a
43	chr10:49710976-49711026	SK-N-SH_RA	brain:	n/a
44	chr10:49710976-49711026	ProgFib	skin:	n/a
45	chr10:49716328-49716378	AG04449	skin:	fetal
46	chr10:49710976-49711026	HMEC	breast:	n/a
47	chr10:49716328-49716378	HUVEC	blood vessel:	n/a
48	chr10:49716328-49716378	AG09309	skin:	n/a
49	chr10:49710976-49711026	ovcar-3	ovarian:	n/a
50	chr10:49716328-49716378	HIPEpiC	eye:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:49615597..49618030-chr10:49714235..49716218,3	K562	blood:
2	chr10:49652137..49653652-chr10:49714272..49715285,12	MCF-7	breast:
3	chr10:49571896..49573651-chr10:49713045..49714727,3	K562	blood:
4	chr10:49677417..49680316-chr10:49708989..49711504,2	K562	blood:
5	chr10:49579606..49581410-chr10:49715776..49718367,2	K562	blood:
6	chr10:49714746..49717330-chr10:49717821..49719600,2	MCF-7	breast:
7	chr10:49571458..49572711-chr10:49713545..49714151,3	MCF-7	breast:
8	chr10:49707073..49711100-chr10:49713490..49716250,3	K562	blood:
9	chr10:49715470..49718862-chr10:49725582..49728629,3	K562	blood:
10	chr10:49652288..49653412-chr10:49712926..49713686,3	K562	blood:
11	chr10:49513508..49515174-chr10:49713887..49715575,2	K562	blood:
12	chr10:49653221..49653731-chr10:49714626..49715186,2	MCF-7	breast:
13	chr10:49423270..49424166-chr10:49714289..49715192,4	K562	blood:
14	chr10:49658339..49659956-chr10:49712653..49715066,2	MCF-7	breast:
15	chr10:49637915..49640231-chr10:49714306..49716127,2	K562	blood:
16	chr10:49516511..49518164-chr10:49717889..49719391,2	K562	blood:
17	chr10:49571375..49572211-chr10:49714319..49715238,7	MCF-7	breast:
18	chr10:49571485..49572253-chr10:49714436..49715142,2	MCF-7	breast:
19	chr10:49714293..49714934-chr10:49863931..49864890,2	MCF-7	breast:
20	chr10:49652071..49653009-chr10:49714464..49715277,3	K562	blood:
21	chr10:49663675..49666041-chr10:49714852..49717938,4	K562	blood:
22	chr10:49652128..49653347-chr10:49713187..49714230,4	MCF-7	breast:
23	chr10:49516068..49518164-chr10:49716922..49719391,2	K562	blood:
24	chr10:49703894..49706471-chr10:49715514..49717897,2	K562	blood:
25	chr10:49676784..49678693-chr10:49717036..49719541,2	K562	blood:
26	chr10:49571145..49574084-chr10:49715215..49717894,2	MCF-7	breast:
27	chr10:49698395..49701025-chr10:49710345..49712604,2	K562	blood:
28	chr10:49698265..49700401-chr10:49714707..49717015,2	K562	blood:
29	chr10:49652272..49653208-chr10:49717878..49718849,3	MCF-7	breast:
30	chr10:49692340..49695073-chr10:49708069..49710836,2	K562	blood:
31	chr10:49574821..49576525-chr10:49722125..49725054,2	K562	blood:
32	chr10:49712691..49716238-chr10:49728195..49733174,5	K562	blood:
33	chr10:49571331..49572802-chr10:49714283..49715560,20	K562	blood:
34	chr10:49715021..49718761-chr10:49720982..49725227,3	K562	blood:
35	chr10:49714562..49719396-chr10:49719920..49724610,6	K562	blood:
36	chr10:49714336..49715131-chr17:58308612..58309289,2	MCF-7	breast:
37	chr10:49517657..49518610-chr10:49713350..49714126,2	MCF-7	breast:
38	chr10:49679191..49679816-chr10:49714272..49714777,2	K562	blood:
39	chr10:49714456..49715089-chr10:49863805..49864755,3	K562	blood:
40	chr10:49652115..49653152-chr10:49714314..49715226,3	MCF-7	breast:
41	chr10:49707073..49711100-chr10:49713490..49716250,3	K562	blood:
42	chr10:49711695..49713826-chr10:49717716..49719906,2	K562	blood:
43	chr10:49714562..49719396-chr10:49719920..49724610,6	K562	blood:
44	chr10:49578295..49578943-chr10:49714392..49715251,2	K562	blood:
45	chr10:49714746..49717330-chr10:49717821..49719600,2	MCF-7	breast:
46	chr10:49707527..49709358-chr10:49712606..49714171,2	K562	blood:
47	chr10:49713648..49715470-chr10:49724741..49727947,3	K562	blood:
48	chr10:49713826..49717579-chr10:49717710..49719906,5	K562	blood:
49	chr10:49571307..49572098-chr10:49717849..49718757,3	MCF-7	breast:
50	chr10:49649446..49650312-chr10:49714228..49715210,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRMPD2-1	chr10:49717904-49719721	NONHSAT013273
2	lnc-FRMPD2-1	chr10:49719578-49719720	NONHSAT013274
3	lnc-FRMPD2-1	chr10:49718568-49718982	ENSG00000248682.1
4	lnc-FRMPD2-1	chr10:49719578-49719632	ENSG00000248682.1
5	lnc-FRMPD2-1	chr10:49718035-49718982	NONHSAT013274

No data

Variant related genes	Relation type
ARHGAP22-IT1	TF binding region
ARHGAP22-IT1	CpG island
ENSG00000252577	chromatin interactions
ENSG00000107643	chromatin interactions
ENSG00000177354	chromatin interactions
ENSG00000236208	chromatin interactions
ENSG00000128805	chromatin interactions
ENSG00000103043	chromatin interactions
ENSG00000248682	chromatin interactions

Extended variants
information (count: 585 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:585 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4838608	chr10:49707942-49707943	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113872459	chr10:49707973-49707974	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs150536665	chr10:49708045-49708046	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553095119	chr10:49708064-49708065	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs533176050	chr10:49708070-49708071	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139671044	chr10:49708072-49708073	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs578013917	chr10:49708104-49708105	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113883508	chr10:49708110-49708111	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538744409	chr10:49708168-49708169	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371296163	chr10:49708193-49708194	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs116626991	chr10:49708211-49708212	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs575071370	chr10:49708224-49708225	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542432348	chr10:49708231-49708232	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs113930313	chr10:49708241-49708242	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560822959	chr10:49708245-49708246	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572807808	chr10:49708255-49708256	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563633698	chr10:49708261-49708262	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564718105	chr10:49708319-49708320	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs532181196	chr10:49708325-49708326	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs141051286	chr10:49708380-49708381	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs370336445	chr10:49708381-49708382	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs202003816	chr10:49708397-49708398	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs57914169	chr10:49708400-49708401	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs199566513	chr10:49708401-49708402	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs200277263	chr10:49708402-49708403	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs568331379	chr10:49708404-49708405	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs201083149	chr10:49708405-49708406	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375451411	chr10:49708472-49708473	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139431605	chr10:49708477-49708478	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531091378	chr10:49708480-49708481	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs116694894	chr10:49708483-49708484	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs12571759	chr10:49708630-49708631	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567910608	chr10:49708655-49708656	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs145322179	chr10:49708656-49708657	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547308269	chr10:49708657-49708658	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369438826	chr10:49708660-49708661	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571546053	chr10:49708762-49708763	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs11593258	chr10:49708763-49708764	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557143218	chr10:49708794-49708795	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113121780	chr10:49708795-49708796	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs7907983	chr10:49708803-49708804	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs535997663	chr10:49708824-49708825	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554355765	chr10:49708826-49708827	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190755838	chr10:49708834-49708835	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113396084	chr10:49708838-49708839	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372551954	chr10:49708842-49708843	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs549981102	chr10:49708861-49708862	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs564800863	chr10:49708891-49708892	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576748830	chr10:49708898-49708899	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535773981	chr10:49708914-49708915	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Schizophrenia	23813976	CNVD
Acute myeloid leukemia	19651601	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Rett syndrome	21593744	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
T-cell primary immunodeficiency	21948486	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:294 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49698000-49731200	Weak transcription	Aorta	Aorta
2	chr10:49701600-49716400	Weak transcription	Right Atrium	heart
3	chr10:49702400-49718200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr10:49705400-49716600	Weak transcription	Brain Angular Gyrus	brain
5	chr10:49705600-49708400	Weak transcription	Esophagus	oesophagus
6	chr10:49705600-49715600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr10:49705800-49713000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr10:49706000-49709200	Weak transcription	NHLF	lung
9	chr10:49706000-49709400	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr10:49706000-49710200	Weak transcription	Fetal Muscle Leg	muscle
11	chr10:49706000-49710600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr10:49706000-49716600	Weak transcription	HMEC	breast
13	chr10:49706000-49723400	Weak transcription	NH-A	brain
14	chr10:49706200-49709200	Weak transcription	Osteobl	bone
15	chr10:49706200-49709400	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr10:49706200-49709800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr10:49706200-49712400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr10:49706200-49712400	Weak transcription	Fetal Thymus	thymus
19	chr10:49706200-49713800	Weak transcription	HSMM	muscle
20	chr10:49706200-49716400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr10:49706400-49709400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr10:49706400-49710400	Weak transcription	HSMMtube	muscle
23	chr10:49706600-49709400	Weak transcription	Ovary	ovary
24	chr10:49706800-49710000	Weak transcription	K562	blood
25	chr10:49707000-49709200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr10:49707200-49709200	Weak transcription	NHDF-Ad	bronchial
27	chr10:49707400-49709200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr10:49707400-49710000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr10:49707400-49716600	Weak transcription	Fetal Stomach	stomach
30	chr10:49707600-49710600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr10:49707600-49716600	Weak transcription	Brain Cingulate Gyrus	brain
32	chr10:49707800-49709000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr10:49707800-49709200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr10:49707800-49709800	Weak transcription	Primary hematopoietic stem cells	blood
35	chr10:49708400-49710800	Enhancers	GM12878-XiMat	blood
36	chr10:49709000-49709800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr10:49709200-49709600	Genic enhancers	Osteobl	bone
38	chr10:49709200-49709800	Enhancers	NHLF	lung
39	chr10:49709200-49711200	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr10:49709200-49711200	Genic enhancers	NHDF-Ad	bronchial
41	chr10:49709200-49712000	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr10:49709200-49712400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr10:49709200-49720600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr10:49709400-49709600	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr10:49709400-49709600	Enhancers	Ovary	ovary
46	chr10:49709400-49711000	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr10:49709400-49712800	Strong transcription	Muscle Satellite Cultured Cells	--
48	chr10:49709400-49713000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr10:49709600-49710000	Weak transcription	Ovary	ovary
50	chr10:49709600-49711600	Strong transcription	Osteobl	bone

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