Variant report

Variant	nsv547965
Chromosome Location	chr1:155563152-155688600
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2690)
CpG islands
(count:1954)
Chromatin interactive
region (count:100)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2690 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:155668433-155668644	K562	blood:	n/a	n/a
2	ARID3A	chr1:155668143-155668584	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:155658644-155658844	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:155669019-155669222	K562	blood:	n/a	n/a
5	ARID3A	chr1:155618383-155618679	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:155658506-155658881	K562	blood:	n/a	n/a
7	ARID3A	chr1:155612277-155612602	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:155661890-155662275	K562	blood:	n/a	n/a
9	ATF1	chr1:155579477-155580032	K562	blood:	n/a	n/a
10	ATF1	chr1:155618388-155618575	K562	blood:	n/a	n/a
11	ATF1	chr1:155619580-155619710	K562	blood:	n/a	n/a
12	ATF1	chr1:155661656-155662250	K562	blood:	n/a	n/a
13	ATF1	chr1:155668826-155669242	K562	blood:	n/a	n/a
14	ATF2	chr1:155579446-155579728	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr1:155658524-155659058	GM12878	blood:	n/a	n/a
16	ATF2	chr1:155657966-155658413	GM12878	blood:	n/a	n/a
17	ATF3	chr1:155579451-155579666	K562	blood:	n/a	n/a
18	ATF3	chr1:155668216-155668483	K562	blood:	n/a	n/a
19	ATF3	chr1:155579342-155579779	GM12878	blood:	n/a	chr1:155579735-155579744
20	ATF3	chr1:155658307-155659029	A549	lung:	n/a	n/a
21	BACH1	chr1:155658661-155658693	K562	blood:	n/a	n/a
22	BACH1	chr1:155618460-155618489	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr1:155657984-155659056	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr1:155579480-155579965	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr1:155686853-155687188	GM12878	blood:	n/a	n/a
26	BATF	chr1:155657407-155657795	GM12878	blood:	n/a	n/a
27	BATF	chr1:155591936-155592215	GM12878	blood:	n/a	n/a
28	BATF	chr1:155591936-155592214	GM12878	blood:	n/a	n/a
29	BCL11A	chr1:155579925-155580267	GM12878	blood:	n/a	n/a
30	BCL11A	chr1:155657352-155657700	GM12878	blood:	n/a	n/a
31	BCL3	chr1:155579304-155579922	A549	lung:	n/a	n/a
32	BCL3	chr1:155644880-155645132	GM12878	blood:	n/a	n/a
33	BCL3	chr1:155658481-155658924	A549	lung:	n/a	n/a
34	BCL3	chr1:155626535-155627461	A549	lung:	n/a	n/a
35	BCL3	chr1:155657883-155658436	A549	lung:	n/a	n/a
36	BCL3	chr1:155579300-155579922	A549	lung:	n/a	n/a
37	BCLAF1	chr1:155657814-155658689	GM12878	blood:	n/a	n/a
38	BCLAF1	chr1:155661762-155662351	K562	blood:	n/a	n/a
39	BCLAF1	chr1:155657912-155658523	GM12878	blood:	n/a	n/a
40	BHLHE40	chr1:155579425-155579967	K562	blood:	n/a	n/a
41	BHLHE40	chr1:155618466-155618716	A549	lung:	n/a	n/a
42	BHLHE40	chr1:155621955-155622078	GM12878	blood:	n/a	n/a
43	BHLHE40	chr1:155658013-155658987	GM12878	blood:	n/a	n/a
44	BHLHE40	chr1:155658487-155658957	A549	lung:	n/a	n/a
45	BHLHE40	chr1:155579413-155579947	GM12878	blood:	n/a	n/a
46	BHLHE40	chr1:155658035-155659053	K562	blood:	n/a	n/a
47	BHLHE40	chr1:155618462-155618505	K562	blood:	n/a	n/a
48	BHLHE40	chr1:155658190-155659012	HepG2	liver:	n/a	n/a
49	BRCA1	chr1:155658595-155658851	HepG2	liver:	n/a	n/a
50	BRCA1	chr1:155658456-155658910	GM12878	blood:	n/a	n/a

(count:1954 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155579369-155579419	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:155659719-155659769	Hela-S3	cervix:	n/a
3	chr1:155579369-155579419	HPAEpiC	pulmonary alveolar:	n/a
4	chr1:155659719-155659769	Hela-S3	cervix:	n/a
5	chr1:155629389-155629439	BE2_C	brain:	n/a
6	chr1:155579900-155579950	BE2_C	brain:	n/a
7	chr1:155579520-155579570	ECC-1	luminal epithelium:	n/a
8	chr1:155641827-155641877	NH-A	brain:	n/a
9	chr1:155579657-155579707	ovcar-3	ovarian:	n/a
10	chr1:155658509-155658559	HMEC	breast:	n/a
11	chr1:155657930-155657980	NB4	blood:	n/a
12	chr1:155654191-155654241	GM06990	blood:	n/a
13	chr1:155579657-155579707	HCM	heart:	n/a
14	chr1:155579738-155579788	SKMC	muscle:	n/a
15	chr1:155579895-155579945	AG09309	skin:	n/a
16	chr1:155663085-155663135	BJ	skin:	n/a
17	chr1:155579817-155579867	HUVEC	blood vessel:	n/a
18	chr1:155658898-155658948	HNPCEpiC	eye:	n/a
19	chr1:155658898-155658948	HCF	heart:	n/a
20	chr1:155658843-155658893	AG09309	skin:	n/a
21	chr1:155659247-155659297	ovcar-3	ovarian:	n/a
22	chr1:155659194-155659244	AG09319	gingival:	n/a
23	chr1:155658933-155658983	Hela-S3	cervix:	n/a
24	chr1:155579738-155579788	SK-N-MC	brain:	n/a
25	chr1:155579900-155579950	HRPEpiC	eye:	n/a
26	chr1:155658576-155658626	HCF	heart:	n/a
27	chr1:155658835-155658885	HMEC	breast:	n/a
28	chr1:155579900-155579950	HRCEpiC	kidney:	n/a
29	chr1:155658835-155658885	HRE	kidney:	n/a
30	chr1:155641827-155641877	HRE	kidney:	n/a
31	chr1:155582325-155582375	HPAEpiC	pulmonary alveolar:	n/a
32	chr1:155615664-155615714	ECC-1	luminal epithelium:	n/a
33	chr1:155658843-155658893	PFSK-1	brain:	n/a
34	chr1:155582969-155583019	GM12878	blood:	n/a
35	chr1:155658843-155658893	GM19239	blood:	n/a
36	chr1:155579657-155579707	AoSMC	blood vessel:	n/a
37	chr1:155582325-155582375	Hepatocyte	liver:	n/a
38	chr1:155579964-155580014	PrEC	prostate:	n/a
39	chr1:155579657-155579707	NHDF-neo	bronchial:	n/a
40	chr1:155579964-155580014	MCF10A-Er-Src	breast:	n/a
41	chr1:155663085-155663135	AoSMC	blood vessel:	n/a
42	chr1:155579520-155579570	AG10803	skin:	n/a
43	chr1:155654191-155654241	CMK	blood:	n/a
44	chr1:155658929-155658979	SAEC	small airway:	n/a
45	chr1:155659719-155659769	GM12878	blood:	n/a
46	chr1:155658929-155658979	HCT-116	colon:	n/a
47	chr1:155658576-155658626	HCPEpiC	choroid plexus:	n/a
48	chr1:155579807-155579857	SAEC	small airway:	n/a
49	chr1:155579738-155579788	HRPEpiC	eye:	n/a
50	chr1:155663085-155663135	MCF10A-Er-Src	breast:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:155624881..155626897-chr1:155647501..155650003,2	K562	blood:
2	chr1:155646937..155653370-chr1:155653884..155660272,11	K562	blood:
3	chr1:155619948..155622617-chr1:155654194..155656266,2	MCF-7	breast:
4	chr1:155639842..155641507-chr1:155653643..155656160,2	MCF-7	breast:
5	chr1:155622742..155624399-chr1:155656561..155659383,2	MCF-7	breast:
6	chr1:155637711..155639651-chr1:155658391..155660374,2	MCF-7	breast:
7	chr1:155632359..155634916-chr1:155641249..155643126,2	MCF-7	breast:
8	chr1:155605649..155607363-chr1:155609157..155610768,2	K562	blood:
9	chr1:155579581..155580433-chr17:66508628..66509408,2	Hela-S3	cervix:
10	chr1:155561838..155563770-chr1:155565772..155568084,2	K562	blood:
11	chr1:155658633..155662039-chr1:156022948..156025065,3	K562	blood:
12	chr1:155579412..155580086-chr10:111683248..111683938,2	NB4	blood:
13	chr1:155650232..155654143-chr1:155656732..155660370,8	MCF-7	breast:
14	chr1:155619365..155621539-chr1:155630413..155632008,2	K562	blood:
15	chr1:155657851..155658412-chr9:98637639..98638211,2	Hela-S3	cervix:
16	chr1:155656893..155661917-chr1:155662515..155668604,13	MCF-7	breast:
17	chr1:155530812..155532531-chr1:155657028..155659724,4	K562	blood:
18	chr1:155565398..155567532-chr1:155573689..155576463,2	MCF-7	breast:
19	chr1:155619948..155622617-chr1:155654194..155656266,2	MCF-7	breast:
20	chr1:155656761..155658571-chr1:155822378..155824933,2	K562	blood:
21	chr1:155585309..155588170-chr1:155594115..155596195,2	MCF-7	breast:
22	chr1:155629015..155630662-chr1:155630856..155633669,2	MCF-7	breast:
23	chr1:155625229..155627200-chr1:155627769..155629453,2	K562	blood:
24	chr1:155657873..155658675-chr15:91415725..91416297,2	Hela-S3	cervix:
25	chr1:155644200..155646562-chr1:155654143..155655754,2	K562	blood:
26	chr1:155641405..155643309-chr1:155647135..155648981,2	K562	blood:
27	chr1:155162636..155164137-chr1:155576415..155579357,2	K562	blood:
28	chr1:155621509..155623036-chr1:155655478..155657409,2	K562	blood:
29	chr1:155293644..155295180-chr1:155658200..155659752,2	MCF-7	breast:
30	chr1:155662296..155664287-chr1:155670196..155672385,2	MCF-7	breast:
31	chr1:155644991..155647996-chr1:155653884..155656777,3	MCF-7	breast:
32	chr1:155247122..155248750-chr1:155618012..155619696,2	MCF-7	breast:
33	chr1:155531220..155534536-chr1:155656727..155659727,4	MCF-7	breast:
34	chr1:155677745..155679785-chr1:155684499..155686373,2	K562	blood:
35	chr1:155585309..155588170-chr1:155594115..155596195,2	MCF-7	breast:
36	chr1:155662296..155664287-chr1:155670196..155672385,2	MCF-7	breast:
37	chr1:155625229..155627200-chr1:155627769..155629453,2	K562	blood:
38	chr1:155648026..155650983-chr1:155651432..155653542,3	K562	blood:
39	chr1:155162487..155164653-chr1:155579583..155581273,2	K562	blood:
40	chr1:155650232..155654143-chr1:155656732..155660370,8	MCF-7	breast:
41	chr1:155621509..155623036-chr1:155655478..155657409,2	K562	blood:
42	chr1:155581980..155584132-chr1:155585540..155587149,2	K562	blood:
43	chr1:155609013..155610519-chr1:155620410..155621940,2	MCF-7	breast:
44	chr1:155632359..155634916-chr1:155641249..155643126,2	MCF-7	breast:
45	chr1:155647841..155650282-chr1:155658064..155659902,2	MCF-7	breast:
46	chr1:155579429..155579947-chr7:27224098..27225019,2	Hela-S3	cervix:
47	chr1:155623481..155626376-chr1:155629925..155633670,3	K562	blood:
48	chr1:155658041..155658876-chr9:75766420..75767093,2	Hela-S3	cervix:
49	chr1:155579443..155580336-chr11:35160348..35160978,2	NB4	blood:
50	chr1:155644925..155647693-chr1:155648033..155650535,4	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DAP3-2	chr1:155580476-155580899	NONHSAT006748
2	lnc-DAP3-1	chr1:155658630-155659128	NONHSAT006756
3	lnc-YY1AP1-1	chr1:155680329-155680354	ENSG00000227673.1
4	lnc-DAP3-1	chr1:155657751-155657983	NONHSAT006756
5	lnc-ASH1L-2	chr1:155579567-155579683	ENSG00000232519.2
6	lnc-ASH1L-2	chr1:155579339-155579683	ENSG00000232519.1
7	lnc-DAP3-1	chr1:155657782-155657983	NONHSAT006758
8	lnc-ASH1L-2	chr1:155580069-155580171	ENSG00000232519.2
9	lnc-DAP3-2	chr1:155581480-155581707	NONHSAT006748
10	lnc-DAP3-2	chr1:155581007-155581394	NONHSAT006748
11	lnc-DAP3-1	chr1:155658886-155659418	NONHSAT006758
12	lnc-ASH1L-2	chr1:155580069-155580171	ENSG00000232519.1
13	lnc-YY1AP1-1	chr1:155679889-155680019	ENSG00000227673.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MSTO1	hsa-miR-10b-5p	chr1:155584021-155584044

Variant related genes	Relation type
DAP3	TF binding region
ENSG00000232519	TF binding region
YY1AP1	TF binding region
MSTO2P	TF binding region
ENSG00000227673	TF binding region
MSTO1	TF binding region
ENSG00000246203	TF binding region
ENSG00000223503	TF binding region
DAP3	CpG island
ENSG00000232519	CpG island
YY1AP1	CpG island
MSTO2P	CpG island
ENSG00000227673	CpG island
MSTO1	CpG island
ENSG00000246203	CpG island
ENSG00000223503	CpG island
ENSG00000116580	chromatin interactions
ENSG00000169231	chromatin interactions
ENSG00000203761	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000160766	chromatin interactions
ENSG00000116539	chromatin interactions
ENSG00000182150	chromatin interactions
ENSG00000162927	chromatin interactions
ENSG00000135046	chromatin interactions
ENSG00000169242	chromatin interactions
ENSG00000246203	chromatin interactions
ENSG00000173171	chromatin interactions
ENSG00000162928	chromatin interactions
ENSG00000125459	chromatin interactions
ENSG00000108946	chromatin interactions
ENSG00000235919	chromatin interactions
ENSG00000128016	chromatin interactions
ENSG00000114107	chromatin interactions
ENSG00000232519	chromatin interactions
ENSG00000160753	chromatin interactions
ENSG00000116586	chromatin interactions
ENSG00000140564	chromatin interactions
ENSG00000240990	chromatin interactions
ENSG00000185499	chromatin interactions
ENSG00000167553	chromatin interactions
ENSG00000225855	chromatin interactions
ENSG00000005073	chromatin interactions
ENSG00000026508	chromatin interactions
ENSG00000160752	chromatin interactions
ENSG00000185630	chromatin interactions
ENSG00000132676	chromatin interactions
ENSG00000160803	chromatin interactions
ENSG00000176444	chromatin interactions
ENSG00000143630	chromatin interactions
ENSG00000160767	chromatin interactions
ENSG00000163374	chromatin interactions
ENSG00000108039	chromatin interactions
ENSG00000258101	chromatin interactions
ENSG00000175611	chromatin interactions

Extended variants
information (count: 4586 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:4586 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11264387	chr1:155563152-155563153	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531822088	chr1:155563171-155563172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550052765	chr1:155563199-155563200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs72997142	chr1:155563329-155563330	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs191267199	chr1:155563346-155563347	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs182588374	chr1:155563395-155563396	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs115029292	chr1:155563454-155563455	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs550617103	chr1:155563482-155563483	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs531376594	chr1:155563488-155563489	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs534081858	chr1:155563496-155563497	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs146558161	chr1:155563497-155563498	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs570395186	chr1:155563499-155563500	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537946002	chr1:155563513-155563514	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs556016870	chr1:155563542-155563543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs574962110	chr1:155563576-155563577	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs372708595	chr1:155563633-155563634	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs553968096	chr1:155563675-155563676	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs111322177	chr1:155563690-155563691	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs547778313	chr1:155563759-155563760	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs546127041	chr1:155563846-155563847	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs567842246	chr1:155563920-155563921	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs564500143	chr1:155563947-155563948	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs551311507	chr1:155563959-155563960	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs186074583	chr1:155563972-155563973	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs191058884	chr1:155563990-155563991	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs562006005	chr1:155564054-155564055	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs57644936	chr1:155564122-155564123	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs541997383	chr1:155564220-155564221	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs183191572	chr1:155564295-155564296	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs527575366	chr1:155564307-155564308	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs570580067	chr1:155564322-155564323	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs552552826	chr1:155564366-155564367	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs570405804	chr1:155564383-155564384	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs71628671	chr1:155564405-155564406	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs531244942	chr1:155564420-155564421	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs187478556	chr1:155564446-155564447	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs539362111	chr1:155564451-155564452	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs568036399	chr1:155564748-155564749	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs535181773	chr1:155564749-155564750	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs553935094	chr1:155564819-155564820	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs565977509	chr1:155564869-155564870	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs539720191	chr1:155564916-155564917	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs11486123	chr1:155564922-155564923	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs11486124	chr1:155564926-155564927	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs549150249	chr1:155564928-155564929	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs576689108	chr1:155564929-155564930	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs34514120	chr1:155564949-155564950	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs562778497	chr1:155564968-155564969	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs35985996	chr1:155564986-155564987	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs543423450	chr1:155565037-155565038	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Dihydropyrimidine dehydrogenase deficiency	18421352	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:3896 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155534600-155565800	Weak transcription	Brain Hippocampus Middle	brain
2	chr1:155534800-155565600	Weak transcription	Brain Angular Gyrus	brain
3	chr1:155534800-155568400	Weak transcription	Thymus	Thymus
4	chr1:155535000-155570400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:155535400-155564000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr1:155540400-155565800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr1:155541400-155569000	Weak transcription	HSMMtube	muscle
8	chr1:155541600-155565600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:155541600-155565600	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr1:155541600-155568400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr1:155542000-155565600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:155554000-155566400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr1:155557200-155568600	Weak transcription	NHEK	skin
14	chr1:155558400-155568600	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr1:155559000-155568800	Weak transcription	HSMM	muscle
16	chr1:155559200-155565600	Weak transcription	Fetal Brain Female	brain
17	chr1:155560600-155565800	Weak transcription	Brain Anterior Caudate	brain
18	chr1:155560600-155568400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr1:155560600-155568400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr1:155560600-155570400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr1:155561000-155568800	Weak transcription	Lung	lung
22	chr1:155561200-155568400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr1:155561200-155568600	Weak transcription	Fetal Stomach	stomach
24	chr1:155561400-155568200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr1:155562000-155564200	Weak transcription	Brain Germinal Matrix	brain
26	chr1:155562200-155565600	Weak transcription	Brain Cingulate Gyrus	brain
27	chr1:155562200-155570200	Weak transcription	Hela-S3	cervix
28	chr1:155564200-155564400	Enhancers	Brain Germinal Matrix	brain
29	chr1:155564400-155565200	Weak transcription	Brain Germinal Matrix	brain
30	chr1:155564600-155567200	Enhancers	Fetal Brain Male	brain
31	chr1:155565200-155565400	Enhancers	Brain Germinal Matrix	brain
32	chr1:155565400-155565800	Flanking Active TSS	Brain Germinal Matrix	brain
33	chr1:155565600-155565800	Flanking Active TSS	Fetal Brain Female	brain
34	chr1:155565600-155566000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr1:155565600-155566600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr1:155565600-155566600	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr1:155565600-155566600	Enhancers	Brain Angular Gyrus	brain
38	chr1:155565600-155567000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr1:155565600-155567000	Enhancers	Brain Cingulate Gyrus	brain
40	chr1:155565800-155566200	Active TSS	Brain Germinal Matrix	brain
41	chr1:155565800-155566200	Active TSS	Fetal Brain Female	brain
42	chr1:155565800-155566600	Enhancers	Brain Anterior Caudate	brain
43	chr1:155565800-155567000	Enhancers	Brain Hippocampus Middle	brain
44	chr1:155565800-155567000	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr1:155566000-155566800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr1:155566200-155566400	Flanking Active TSS	Fetal Brain Female	brain
47	chr1:155566200-155566600	Flanking Active TSS	Brain Germinal Matrix	brain
48	chr1:155566200-155566600	Enhancers	Brain Substantia Nigra	brain
49	chr1:155566400-155566600	Enhancers	Fetal Brain Female	brain
50	chr1:155566400-155567000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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