Variant report

Variant	esv3426992
Chromosome Location	chr7:6675227-6678325
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:659)
CpG islands
(count:549)
Chromatin interactive
region (count:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:659 , 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	ATF2	chr7:6676670-6676974	GM12878	blood:	n/a	n/a
2	ATF3	chr7:6676663-6677108	GM12878	blood:	n/a	n/a
3	ATF3	chr7:6676764-6677038	K562	blood:	n/a	n/a
4	ATF3	chr7:6676729-6677016	HepG2	liver:	n/a	n/a
5	ATF3	chr7:6676775-6677020	GM12878	blood:	n/a	n/a
6	BACH1	chr7:6676690-6676978	K562	blood:	n/a	n/a
7	BACH1	chr7:6676413-6677735	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:6677373-6677430	K562	blood:	n/a	n/a
9	BCL3	chr7:6676620-6677051	GM12878	blood:	n/a	chr7:6676897-6676906
10	BCLAF1	chr7:6676612-6677075	GM12878	blood:	n/a	chr7:6676897-6676906
11	BHLHE40	chr7:6676722-6677023	K562	blood:	n/a	n/a
12	BHLHE40	chr7:6676405-6676427	K562	blood:	n/a	n/a
13	BHLHE40	chr7:6676643-6677601	GM12878	blood:	n/a	chr7:6677407-6677423
14	BHLHE40	chr7:6677264-6677647	K562	blood:	n/a	chr7:6677407-6677423
15	CBX3	chr7:6677286-6677693	K562	blood:	n/a	n/a
16	CBX3	chr7:6676642-6676930	K562	blood:	n/a	n/a
17	CCNT2	chr7:6676308-6677623	K562	blood:	n/a	n/a
18	CEBPD	chr7:6676684-6677078	K562	blood:	n/a	n/a
19	CEBPD	chr7:6676750-6677014	HepG2	liver:	n/a	n/a
20	CEBPD	chr7:6676694-6677135	HepG2	liver:	n/a	n/a
21	CHD1	chr7:6677295-6677418	GM12878	blood:	n/a	n/a
22	CHD1	chr7:6677773-6677776	GM12878	blood:	n/a	n/a
23	CHD1	chr7:6676646-6677040	GM12878	blood:	n/a	n/a
24	CHD2	chr7:6677366-6677690	GM12878	blood:	n/a	n/a
25	CHD2	chr7:6676556-6676576	HepG2	liver:	n/a	n/a
26	CHD2	chr7:6676748-6676948	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr7:6676738-6677050	GM12878	blood:	n/a	n/a
28	CHD2	chr7:6677612-6677707	K562	blood:	n/a	n/a
29	CREB1	chr7:6676488-6677125	HepG2	liver:	n/a	n/a
30	CREB1	chr7:6676419-6677071	A549	lung:	n/a	n/a
31	CREB1	chr7:6677194-6677588	A549	lung:	n/a	n/a
32	CREB1	chr7:6676811-6676987	A549	lung:	n/a	n/a
33	CTBP2	chr7:6677257-6677706	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr7:6677460-6677610	AG04449	skin:	n/a	n/a
35	CTCF	chr7:6677134-6677893	SK-N-SH	brain:	n/a	chr7:6677332-6677345
36	CTCF	chr7:6677420-6677570	NHLF	lung:	n/a	n/a
37	CTCF	chr7:6677375-6677664	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr7:6677420-6677570	GM12875	blood:	n/a	n/a
39	CTCF	chr7:6677440-6677590	GM12874	blood:	n/a	n/a
40	CTCF	chr7:6677460-6677610	BJ	skin:	n/a	n/a
41	CTCF	chr7:6677460-6677610	GM12865	blood:	n/a	n/a
42	CTCF	chr7:6677320-6677470	HCT-116	colon:	n/a	chr7:6677332-6677345
43	CTCF	chr7:6677331-6677687	K562	blood:	n/a	chr7:6677332-6677345
44	CTCF	chr7:6677460-6677610	Caco-2	colon:	n/a	n/a
45	CTCF	chr7:6677460-6677610	HVMF	connective:	n/a	n/a
46	CTCF	chr7:6677187-6677690	K562	blood:	n/a	chr7:6677332-6677345
47	CTCF	chr7:6677398-6677638	GM12878	blood:	n/a	n/a
48	CTCF	chr7:6677420-6677570	HAc	cerebellar:	n/a	n/a
49	CTCF	chr7:6677400-6677550	NHEK	skin:	n/a	n/a
50	CTCF	chr7:6677540-6677690	WI-38	lung:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6677494-6677544	HCM	heart:	n/a
2	chr7:6676784-6676834	HIPEpiC	eye:	n/a
3	chr7:6677494-6677544	HIPEpiC	eye:	n/a
4	chr7:6676168-6676218	H1-hESC	embryonic stem cell:	embryo
5	chr7:6676832-6676882	MCF10A-Er-Src	breast:	n/a
6	chr7:6676832-6676882	GM12878	blood:	n/a
7	chr7:6677494-6677544	BE2_C	brain:	n/a
8	chr7:6677606-6677656	SK-N-SH	brain:	n/a
9	chr7:6676832-6676882	PANC-1	pancreas:	n/a
10	chr7:6677265-6677315	SK-N-SH_RA	brain:	n/a
11	chr7:6677433-6677483	GM12892	blood:	n/a
12	chr7:6676784-6676834	H1-hESC	embryonic stem cell:	embryo
13	chr7:6676168-6676218	AG10803	skin:	n/a
14	chr7:6677265-6677315	HNPCEpiC	eye:	n/a
15	chr7:6676630-6676680	PFSK-1	brain:	n/a
16	chr7:6677494-6677544	AG09309	skin:	n/a
17	chr7:6677433-6677483	GM19239	blood:	n/a
18	chr7:6677494-6677544	NHDF-neo	bronchial:	n/a
19	chr7:6677494-6677544	HRE	kidney:	n/a
20	chr7:6677433-6677483	A549	lung:	n/a
21	chr7:6676168-6676218	Hepatocyte	liver:	n/a
22	chr7:6677606-6677656	Caco-2	colon:	n/a
23	chr7:6677433-6677483	NHBE	bronchial:	n/a
24	chr7:6676168-6676218	HCF	heart:	n/a
25	chr7:6677494-6677544	HAEpiC	amniotic membrane:	n/a
26	chr7:6677265-6677315	SKMC	muscle:	n/a
27	chr7:6676784-6676834	Caco-2	colon:	n/a
28	chr7:6677494-6677544	AG10803	skin:	n/a
29	chr7:6677433-6677483	ovcar-3	ovarian:	n/a
30	chr7:6676168-6676218	NHDF-neo	bronchial:	n/a
31	chr7:6676784-6676834	HPAEpiC	pulmonary alveolar:	n/a
32	chr7:6677433-6677483	ProgFib	skin:	n/a
33	chr7:6676784-6676834	AG04450	lung:	fetal
34	chr7:6677606-6677656	SKMC	muscle:	n/a
35	chr7:6676001-6676051	NHBE	bronchial:	n/a
36	chr7:6676168-6676218	SK-N-MC	brain:	n/a
37	chr7:6676001-6676051	ECC-1	luminal epithelium:	n/a
38	chr7:6677494-6677544	HMEC	breast:	n/a
39	chr7:6676784-6676834	HAEpiC	amniotic membrane:	n/a
40	chr7:6676630-6676680	HepG2	liver:	n/a
41	chr7:6676001-6676051	HIPEpiC	eye:	n/a
42	chr7:6676001-6676051	IMR90	lung:	fetal
43	chr7:6676168-6676218	BJ	skin:	n/a
44	chr7:6677433-6677483	HRE	kidney:	n/a
45	chr7:6677265-6677315	HPAEpiC	pulmonary alveolar:	n/a
46	chr7:6677433-6677483	AG09309	skin:	n/a
47	chr7:6677494-6677544	HUVEC	blood vessel:	n/a
48	chr7:6676168-6676218	IMR90	lung:	fetal
49	chr7:6677606-6677656	HEK293	kidney:	embryo
50	chr7:6677265-6677315	HMEC	breast:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6628215..6631115-chr7:6675239..6679126,9	MCF-7	breast:
2	chr7:6615703..6619364-chr7:6676501..6679314,4	K562	blood:
3	chr10:104155341..104155841-chr7:6676464..6677005,2	Hela-S3	cervix:
4	chr7:6674043..6676883-chr7:6677067..6680291,5	K562	blood:
5	chr17:41465185..41465700-chr7:6676633..6677215,2	Hela-S3	cervix:
6	chr17:57920745..57921576-chr7:6676970..6677850,2	HCT-116	colon:
7	chr7:6570467..6572933-chr7:6675256..6676794,2	MCF-7	breast:
8	chr7:6677446..6679002-chr7:6745294..6747715,2	K562	blood:
9	chr7:6615800..6617832-chr7:6677563..6680150,2	MCF-7	breast:
10	chr7:6637338..6640081-chr7:6675258..6678566,5	MCF-7	breast:
11	chr7:6626891..6631453-chr7:6677284..6679167,4	K562	blood:
12	chr7:6652934..6655791-chr7:6675915..6678392,2	MCF-7	breast:
13	chr7:6641654..6643210-chr7:6674814..6676517,2	MCF-7	breast:
14	chr7:6654514..6658630-chr7:6675114..6678876,5	MCF-7	breast:
15	chr7:6629079..6630175-chr7:6676992..6678000,4	MCF-7	breast:
16	chr7:6522385..6525546-chr7:6675389..6679461,5	MCF-7	breast:
17	chr7:6627001..6634994-chr7:6673643..6681623,15	MCF-7	breast:
18	chr7:6541950..6543739-chr7:6677071..6679453,2	K562	blood:
19	chr7:6674043..6676883-chr7:6677067..6680291,5	K562	blood:
20	chr7:6626891..6631454-chr7:6676260..6679154,6	K562	blood:
21	chr7:6676193..6679067-chr7:6744810..6746794,4	K562	blood:
22	chr7:6676518..6678447-chr7:6694438..6696514,2	MCF-7	breast:
23	chr7:6675529..6677980-chr7:6768487..6770695,2	K562	blood:
24	chr7:6675962..6678642-chr7:6744432..6748032,4	MCF-7	breast:
25	chr12:56510812..56512603-chr7:6677169..6678802,2	MCF-7	breast:

No data

Variant related genes	Relation type
ZNF316	TF binding region
ZNF316	CpG island
ENSG00000077150	chromatin interactions
ENSG00000146576	chromatin interactions
ENSG00000136240	chromatin interactions
ENSG00000164631	chromatin interactions
ENSG00000135482	chromatin interactions
ENSG00000232581	chromatin interactions
ENSG00000136247	chromatin interactions
ENSG00000215045	chromatin interactions
ENSG00000269781	chromatin interactions
ENSG00000236609	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000139641	chromatin interactions
ENSG00000187953	chromatin interactions
ENSG00000260054	chromatin interactions

Extended variants
information (count: 97 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:97 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375661135	chr7:6675280-6675281	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs530692936	chr7:6675287-6675288	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs549292648	chr7:6675295-6675296	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs567315000	chr7:6675303-6675304	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs10271259	chr7:6675323-6675324	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs546672703	chr7:6675385-6675386	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs532783572	chr7:6675386-6675387	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs189273485	chr7:6675395-6675396	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs148367015	chr7:6675489-6675490	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs575342063	chr7:6675579-6675580	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs536531907	chr7:6675601-6675602	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs141415122	chr7:6675659-6675660	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs181943512	chr7:6675697-6675698	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs540827243	chr7:6675703-6675704	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs554731234	chr7:6675726-6675727	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs576920967	chr7:6675728-6675729	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs114357190	chr7:6675743-6675744	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs570231374	chr7:6675796-6675797	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs530122115	chr7:6675808-6675809	Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs183531427	chr7:6675825-6675826	Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs189194481	chr7:6675829-6675830	Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs569614066	chr7:6675835-6675836	Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs7783767	chr7:6675837-6675838	Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs546809181	chr7:6675850-6675851	Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs139247998	chr7:6675887-6675888	Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs532225807	chr7:6675899-6675900	Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs550731760	chr7:6675962-6675963	Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs562603199	chr7:6675981-6675982	Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs111758928	chr7:6676019-6676020	Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs181129523	chr7:6676059-6676060	Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs548515620	chr7:6676081-6676082	Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs566759151	chr7:6676105-6676106	Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs150018232	chr7:6676125-6676126	Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs186320648	chr7:6676136-6676137	Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs567141670	chr7:6676166-6676167	Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs115824025	chr7:6676168-6676169	Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs146084674	chr7:6676181-6676182	Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs577056380	chr7:6676229-6676230	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs544264471	chr7:6676250-6676251	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs576201195	chr7:6676255-6676256	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs191612498	chr7:6676260-6676261	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs60232048	chr7:6676285-6676286	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs542217285	chr7:6676297-6676298	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs560325781	chr7:6676312-6676313	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs528384307	chr7:6676349-6676350	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs35552150	chr7:6676363-6676364	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs181531594	chr7:6676385-6676386	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs558804923	chr7:6676417-6676418	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs532365722	chr7:6676515-6676516	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs527577728	chr7:6676567-6676568	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20685689	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6656000-6676000	Weak transcription	Psoas Muscle	Psoas
2	chr7:6656200-6675800	Weak transcription	HSMM	muscle
3	chr7:6656800-6675800	Weak transcription	Fetal Brain Male	brain
4	chr7:6660200-6676000	Weak transcription	Colonic Mucosa	Colon
5	chr7:6661800-6675800	Weak transcription	Pancreas	Pancrea
6	chr7:6661800-6676000	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr7:6661800-6676200	Weak transcription	Right Atrium	heart
8	chr7:6662800-6676000	Weak transcription	Colon Smooth Muscle	Colon
9	chr7:6663200-6676000	Weak transcription	Brain Anterior Caudate	brain
10	chr7:6663200-6676000	Weak transcription	Rectal Smooth Muscle	rectum
11	chr7:6663800-6676000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:6663800-6676000	Weak transcription	Brain Angular Gyrus	brain
13	chr7:6663800-6676000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr7:6663800-6676000	Weak transcription	Brain Substantia Nigra	brain
15	chr7:6663800-6676000	Weak transcription	Fetal Intestine Large	intestine
16	chr7:6663800-6676000	Weak transcription	Gastric	stomach
17	chr7:6663800-6676000	Weak transcription	Left Ventricle	heart
18	chr7:6663800-6676000	Weak transcription	Lung	lung
19	chr7:6663800-6676000	Weak transcription	Right Ventricle	heart
20	chr7:6663800-6676000	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr7:6664000-6675800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr7:6664000-6676000	Weak transcription	Brain Cingulate Gyrus	brain
23	chr7:6664200-6676000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr7:6664200-6676000	Weak transcription	Ovary	ovary
25	chr7:6664400-6676000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr7:6665200-6675800	Weak transcription	Stomach Smooth Muscle	stomach
27	chr7:6665200-6676000	Weak transcription	Brain Germinal Matrix	brain
28	chr7:6665400-6675800	Weak transcription	Fetal Lung	lung
29	chr7:6665400-6675800	Weak transcription	Fetal Muscle Leg	muscle
30	chr7:6665400-6676000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr7:6665400-6676000	Weak transcription	Brain Hippocampus Middle	brain
32	chr7:6665600-6675800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr7:6665600-6676000	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr7:6666000-6676000	Weak transcription	Fetal Brain Female	brain
35	chr7:6670400-6676000	Weak transcription	Fetal Intestine Small	intestine
36	chr7:6670600-6676000	Weak transcription	Placenta	Placenta
37	chr7:6671800-6675800	Weak transcription	HMEC	breast
38	chr7:6672000-6676000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr7:6674000-6675600	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
40	chr7:6674200-6676000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr7:6674400-6676200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr7:6674600-6676000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr7:6674800-6675600	ZNF genes & repeats	GM12878-XiMat	blood
44	chr7:6674800-6675800	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr7:6674800-6676200	Enhancers	Primary B cells from peripheral blood	blood
46	chr7:6675000-6675600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
47	chr7:6675000-6676000	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr7:6675000-6676800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr7:6675200-6675400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr7:6675200-6675400	Enhancers	Esophagus	oesophagus

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