Variant report

Variant	esv3438606
Chromosome Location	chr15:76134422-76137270
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:650)
CpG islands
(count:550)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:650 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:76136649-76136842	K562	blood:	n/a	n/a
2	BACH1	chr15:76135149-76136412	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr15:76135787-76136602	A549	lung:	n/a	n/a
4	BCL3	chr15:76134802-76135669	A549	lung:	n/a	n/a
5	BCLAF1	chr15:76135109-76136026	GM12878	blood:	n/a	n/a
6	BHLHE40	chr15:76135323-76135609	A549	lung:	n/a	chr15:76135323-76135339 chr15:76135394-76135410 chr15:76135523-76135539
7	BHLHE40	chr15:76134966-76136386	K562	blood:	n/a	chr15:76135323-76135339 chr15:76135394-76135410 chr15:76135523-76135539 chr15:76135772-76135788
8	BHLHE40	chr15:76136631-76137223	K562	blood:	n/a	n/a
9	BHLHE40	chr15:76136367-76136816	GM12878	blood:	n/a	chr15:76136461-76136477
10	BHLHE40	chr15:76135173-76135958	GM12878	blood:	n/a	chr15:76135323-76135339 chr15:76135394-76135410 chr15:76135523-76135539 chr15:76135772-76135788
11	BHLHE40	chr15:76135137-76135845	HepG2	liver:	n/a	chr15:76135323-76135339 chr15:76135394-76135410 chr15:76135523-76135539 chr15:76135772-76135788
12	BRCA1	chr15:76136220-76136407	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr15:76135411-76135524	HepG2	liver:	n/a	n/a
14	CBX3	chr15:76136494-76136979	K562	blood:	n/a	n/a
15	CBX3	chr15:76135000-76135910	K562	blood:	n/a	n/a
16	CCNT2	chr15:76135080-76136768	K562	blood:	n/a	chr15:76135698-76135707
17	CEBPB	chr15:76134391-76134654	K562	blood:	n/a	n/a
18	CEBPD	chr15:76135289-76136090	HepG2	liver:	n/a	n/a
19	CHD1	chr15:76136557-76137192	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr15:76135922-76137076	GM12878	blood:	n/a	n/a
21	CHD1	chr15:76136098-76136290	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD1	chr15:76135144-76135360	GM12878	blood:	n/a	chr15:76135191-76135201
23	CHD2	chr15:76135101-76135752	K562	blood:	n/a	chr15:76135191-76135201 chr15:76135699-76135709
24	CHD2	chr15:76136262-76136424	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr15:76135497-76135631	HepG2	liver:	n/a	n/a
26	CHD2	chr15:76135430-76136912	Hela-S3	cervix:	n/a	chr15:76135699-76135709
27	CHD2	chr15:76135029-76135841	H1-hESC	embryonic stem cell:	n/a	chr15:76135191-76135201 chr15:76135699-76135709
28	CHD2	chr15:76135988-76136502	K562	blood:	n/a	n/a
29	CHD2	chr15:76135187-76136833	GM12878	blood:	n/a	chr15:76135191-76135201 chr15:76135699-76135709
30	CHD2	chr15:76136049-76136449	HepG2	liver:	n/a	n/a
31	CREB1	chr15:76135020-76136791	HepG2	liver:	n/a	n/a
32	CREB1	chr15:76135071-76136580	A549	lung:	n/a	n/a
33	CREB1	chr15:76135248-76135607	A549	lung:	n/a	n/a
34	CREB1	chr15:76135189-76136279	GM12878	blood:	n/a	n/a
35	CTCF	chr15:76135120-76135270	HepG2	liver:	n/a	chr15:76135140-76135149
36	CTCF	chr15:76135158-76135437	K562	blood:	n/a	chr15:76135395-76135408 chr15:76135398-76135407
37	CTCF	chr15:76135700-76135850	AG04449	skin:	n/a	chr15:76135779-76135792 chr15:76135773-76135786 chr15:76135776-76135789
38	CTCF	chr15:76136500-76136650	AoAF	blood vessel:	n/a	chr15:76136502-76136515
39	CTCF	chr15:76136771-76136822	GM12892	blood:	n/a	n/a
40	CTCF	chr15:76136175-76136206	GM13976	blood:	n/a	n/a
41	CTCF	chr15:76136640-76136790	HCM	heart:	n/a	n/a
42	CTCF	chr15:76136120-76136270	GM12865	blood:	n/a	n/a
43	CTCF	chr15:76136100-76136250	AG04449	skin:	n/a	n/a
44	CTCF	chr15:76135080-76135230	GM12867	blood:	n/a	chr15:76135140-76135149
45	CTCF	chr15:76135140-76135290	GM12873	blood:	n/a	chr15:76135140-76135149
46	CTCF	chr15:76135140-76135290	HEK293	kidney:	n/a	chr15:76135140-76135149
47	CTCF	chr15:76136140-76136177	MCF-7	breast:	n/a	n/a
48	CTCF	chr15:76136168-76136203	GM12892	blood:	n/a	n/a
49	CTCF	chr15:76135980-76136130	SAEC	small airway:	n/a	n/a
50	CTCF	chr15:76136420-76136570	A549	lung:	n/a	chr15:76136502-76136515

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76135159-76135209	GM12878	blood:	n/a
2	chr15:76135159-76135209	GM12878	blood:	n/a
3	chr15:76136129-76136179	H1-hESC	embryonic stem cell:	embryo
4	chr15:76136875-76136925	ovcar-3	ovarian:	n/a
5	chr15:76136846-76136896	AG04450	lung:	fetal
6	chr15:76136129-76136179	GM06990	blood:	n/a
7	chr15:76135159-76135209	HCPEpiC	choroid plexus:	n/a
8	chr15:76136875-76136925	K562	blood:	n/a
9	chr15:76136437-76136487	NH-A	brain:	n/a
10	chr15:76136129-76136179	ECC-1	luminal epithelium:	n/a
11	chr15:76135744-76135794	GM06990	blood:	n/a
12	chr15:76136386-76136436	RPTEC	kidney:	n/a
13	chr15:76136386-76136436	SK-N-SH	brain:	n/a
14	chr15:76136129-76136179	SK-N-SH	brain:	n/a
15	chr15:76136437-76136487	CMK	blood:	n/a
16	chr15:76135312-76135362	HPAEpiC	pulmonary alveolar:	n/a
17	chr15:76135744-76135794	GM12891	blood:	n/a
18	chr15:76136386-76136436	GM19239	blood:	n/a
19	chr15:76135159-76135209	HMEC	breast:	n/a
20	chr15:76135284-76135334	ProgFib	skin:	n/a
21	chr15:76136386-76136436	HAEpiC	amniotic membrane:	n/a
22	chr15:76136437-76136487	HCPEpiC	choroid plexus:	n/a
23	chr15:76136437-76136487	HUVEC	blood vessel:	n/a
24	chr15:76136846-76136896	AoSMC	blood vessel:	n/a
25	chr15:76136129-76136179	IMR90	lung:	fetal
26	chr15:76136875-76136925	PANC-1	pancreas:	n/a
27	chr15:76135744-76135794	ProgFib	skin:	n/a
28	chr15:76135744-76135794	HRCEpiC	kidney:	n/a
29	chr15:76135312-76135362	K562	blood:	n/a
30	chr15:76135312-76135362	NHBE	bronchial:	n/a
31	chr15:76135284-76135334	SKMC	muscle:	n/a
32	chr15:76135312-76135362	NT2-D1	testis:	n/a
33	chr15:76135284-76135334	LNCaP	prostate:	n/a
34	chr15:76136875-76136925	IMR90	lung:	fetal
35	chr15:76135744-76135794	GM12892	blood:	n/a
36	chr15:76135744-76135794	HCT-116	colon:	n/a
37	chr15:76135312-76135362	MCF-7	breast:	n/a
38	chr15:76135159-76135209	HRE	kidney:	n/a
39	chr15:76136846-76136896	Hepatocyte	liver:	n/a
40	chr15:76136437-76136487	U87	brain:	n/a
41	chr15:76135312-76135362	IMR90	lung:	fetal
42	chr15:76135159-76135209	A549	lung:	n/a
43	chr15:76136386-76136436	U87	brain:	n/a
44	chr15:76136846-76136896	HCM	heart:	n/a
45	chr15:76135312-76135362	SKMC	muscle:	n/a
46	chr15:76136846-76136896	AG04449	skin:	fetal
47	chr15:76135312-76135362	AG09309	skin:	n/a
48	chr15:76135284-76135334	NHBE	bronchial:	n/a
49	chr15:76136846-76136896	NHBE	bronchial:	n/a
50	chr15:76135744-76135794	IMR90	lung:	fetal

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:76133453..76135446-chr15:76194231..76197164,2	MCF-7	breast:
2	chr15:76135389..76135908-chr5:176853550..176854343,2	Hela-S3	cervix:
3	chr15:76137201..76139115-chr15:76170470..76172779,2	K562	blood:
4	chr15:76133681..76139746-chr15:76193985..76199740,23	MCF-7	breast:
5	chr15:76134992..76136572-chr15:76350644..76353343,2	MCF-7	breast:
6	chr15:76135754..76137278-chr15:76196181..76197882,2	K562	blood:
7	chr15:76133451..76137775-chr15:76156108..76161375,6	MCF-7	breast:
8	chr15:76133553..76135071-chr15:76150512..76152325,2	MCF-7	breast:
9	chr15:75917263..75918956-chr15:76135075..76137725,2	K562	blood:
10	chr12:69081083..69082998-chr15:76135423..76138290,2	MCF-7	breast:
11	chr15:76136320..76138116-chr15:76204520..76207096,2	MCF-7	breast:
12	chr15:76136933..76140770-chr15:76154598..76157335,3	K562	blood:
13	chr15:76135493..76137289-chr15:76195431..76198634,3	MCF-7	breast:
14	chr15:75659414..75661741-chr15:76133150..76135870,3	K562	blood:
15	chr15:76135545..76137145-chr15:76186509..76188555,3	MCF-7	breast:
16	chr15:76120011..76122209-chr15:76134014..76135562,2	MCF-7	breast:
17	chr15:76066670..76069216-chr15:76135374..76137197,2	MCF-7	breast:
18	chr1:172412703..172413401-chr15:76135877..76136831,2	Hela-S3	cervix:
19	chr15:76134186..76138083-chr15:76192925..76200499,13	K562	blood:
20	chr15:75660482..75662699-chr15:76134018..76135657,2	MCF-7	breast:

No data

Variant related genes	Relation type
UBE2Q2	TF binding region
UBE2Q2	CpG island
ENSG00000187812	chromatin interactions
ENSG00000169758	chromatin interactions
ENSG00000140400	chromatin interactions
ENSG00000140367	chromatin interactions
ENSG00000198055	chromatin interactions
ENSG00000260274	chromatin interactions
ENSG00000111581	chromatin interactions
ENSG00000169752	chromatin interactions
ENSG00000247363	chromatin interactions
ENSG00000167196	chromatin interactions
ENSG00000169371	chromatin interactions
ENSG00000135845	chromatin interactions
ENSG00000266308	chromatin interactions

Extended variants
information (count: 126 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:126 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546703205	chr15:76134440-76134441	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs115107637	chr15:76134444-76134445	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs370196862	chr15:76134445-76134446	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs8182013	chr15:76134458-76134459	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs551239869	chr15:76134466-76134467	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs569488309	chr15:76134507-76134508	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs564519416	chr15:76134527-76134528	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs60496608	chr15:76134544-76134545	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs116439896	chr15:76134545-76134546	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs566482287	chr15:76134559-76134560	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs148486834	chr15:76134575-76134576	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs8182037	chr15:76134601-76134602	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs540507654	chr15:76134608-76134609	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs555532346	chr15:76134612-76134613	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs77130738	chr15:76134646-76134647	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs544121927	chr15:76134665-76134666	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs556420975	chr15:76134669-76134670	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs577815103	chr15:76134671-76134672	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs57090077	chr15:76134685-76134686	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs564106755	chr15:76134714-76134715	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs542946614	chr15:76134881-76134882	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs79646556	chr15:76134885-76134886	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs540306444	chr15:76134903-76134904	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs562075269	chr15:76134934-76134935	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs1665763	chr15:76134988-76134989	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs184581050	chr15:76134994-76134995	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs556895177	chr15:76135021-76135022	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs188502870	chr15:76135030-76135031	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs529219910	chr15:76135053-76135054	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs138239549	chr15:76135057-76135058	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs563097959	chr15:76135169-76135170	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs531233385	chr15:76135176-76135177	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs549387235	chr15:76135209-76135210	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs146305767	chr15:76135221-76135222	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs199987692	chr15:76135255-76135256	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs372427677	chr15:76135347-76135348	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs552117414	chr15:76135367-76135368	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs566456558	chr15:76135376-76135377	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs533807959	chr15:76135412-76135413	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs549093015	chr15:76135420-76135421	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs539560307	chr15:76135483-76135484	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
42	rs567297107	chr15:76135539-76135540	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
43	rs537950038	chr15:76135556-76135557	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
44	rs575192447	chr15:76135705-76135706	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
45	rs577785491	chr15:76135717-76135718	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
46	rs538516201	chr15:76135766-76135767	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
47	rs191949328	chr15:76135814-76135815	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
48	rs572885667	chr15:76135817-76135818	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
49	rs540271849	chr15:76135833-76135834	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
50	rs139614840	chr15:76135874-76135875	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21364760	CNVD
XY gonadal dysgenesis	20685758	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76125200-76134800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr15:76126200-76135000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr15:76129400-76135000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr15:76129600-76134800	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr15:76129600-76135000	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr15:76129600-76135000	Weak transcription	Fetal Heart	heart
7	chr15:76129600-76135200	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr15:76129800-76134800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr15:76129800-76134800	Weak transcription	Osteobl	bone
10	chr15:76129800-76135000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr15:76129800-76135000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr15:76129800-76135000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr15:76129800-76135000	Weak transcription	Duodenum Mucosa	Duodenum
14	chr15:76130000-76134800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr15:76130000-76134800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr15:76130000-76134800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr15:76130000-76134800	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr15:76130000-76135000	Weak transcription	Primary hematopoietic stem cells	blood
19	chr15:76130000-76135000	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr15:76130000-76135000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr15:76130000-76135000	Weak transcription	NHLF	lung
22	chr15:76130400-76135000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr15:76130600-76134800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr15:76130600-76135000	Weak transcription	HSMM	muscle
25	chr15:76131600-76134800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr15:76131600-76134800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr15:76131800-76134600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr15:76131800-76135000	Weak transcription	NHEK	skin
29	chr15:76132000-76135000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr15:76132000-76135000	Weak transcription	HMEC	breast
31	chr15:76132800-76135000	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr15:76133000-76134600	Enhancers	K562	blood
33	chr15:76133000-76135000	Enhancers	Fetal Stomach	stomach
34	chr15:76133200-76135000	Weak transcription	Left Ventricle	heart
35	chr15:76133400-76134600	Weak transcription	Fetal Lung	lung
36	chr15:76133400-76134600	Weak transcription	A549	lung
37	chr15:76133400-76134800	Weak transcription	Colon Smooth Muscle	Colon
38	chr15:76133400-76134800	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr15:76133400-76135000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr15:76133400-76135000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr15:76133400-76135000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr15:76133400-76135000	Weak transcription	Brain Germinal Matrix	brain
43	chr15:76133400-76135000	Weak transcription	Ovary	ovary
44	chr15:76133400-76135000	Weak transcription	Small Intestine	intestine
45	chr15:76133400-76135000	Weak transcription	Hela-S3	cervix
46	chr15:76133400-76135000	Weak transcription	NH-A	brain
47	chr15:76133400-76135000	Weak transcription	NHDF-Ad	bronchial
48	chr15:76133600-76134800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr15:76133600-76135000	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr15:76133600-76135000	Weak transcription	Adipose Nuclei	Adipose

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