Variant report

Variant	nsv831149
Chromosome Location	chr7:136831665-137006468
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:608)
CpG islands
(count:1164)
Chromatin interactive
region (count:41)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:608 , 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	chr7:136853987-136854164	HepG2	liver:	n/a	n/a
2	ATF2	chr7:136853857-136854307	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:136853848-136854381	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:136992921-136992933	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:136880818-136881042	K562	blood:	n/a	n/a
6	BACH1	chr7:136853886-136854162	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:136880793-136881122	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr7:136856791-136856855	GM12878	blood:	n/a	n/a
9	CEBPB	chr7:136856746-136856949	IMR90	lung:	n/a	chr7:136856865-136856876
10	CEBPB	chr7:136918947-136919088	HepG2	liver:	n/a	chr7:136919023-136919034
11	CEBPB	chr7:136851161-136851454	IMR90	lung:	n/a	chr7:136851307-136851316
12	CEBPB	chr7:136956417-136956716	HepG2	liver:	n/a	chr7:136956559-136956570
13	CEBPB	chr7:136928509-136928742	HepG2	liver:	n/a	n/a
14	CEBPB	chr7:136911820-136911980	A549	lung:	n/a	n/a
15	CEBPB	chr7:136915386-136915658	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:136915475-136915645	A549	lung:	n/a	n/a
17	CEBPB	chr7:136835316-136835641	IMR90	lung:	n/a	n/a
18	CEBPB	chr7:136856735-136856935	A549	lung:	n/a	chr7:136856865-136856876
19	CEBPB	chr7:136851292-136851308	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr7:136894300-136894467	HepG2	liver:	n/a	chr7:136894391-136894402
21	CEBPB	chr7:136915432-136915693	IMR90	lung:	n/a	n/a
22	CEBPB	chr7:136945439-136945666	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr7:136830658-136831982	IMR90	lung:	n/a	n/a
24	CEBPB	chr7:136856710-136857042	HepG2	liver:	n/a	chr7:136856865-136856876
25	CEBPB	chr7:136853989-136854249	H1-hESC	embryonic stem cell:	n/a	chr7:136854153-136854165
26	CEBPB	chr7:136851211-136851370	K562	blood:	n/a	chr7:136851307-136851316
27	CEBPB	chr7:136947739-136947900	IMR90	lung:	n/a	n/a
28	CHD2	chr7:136853979-136854259	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr7:136854040-136854190	AoAF	blood vessel:	n/a	chr7:136854107-136854128
30	CTCF	chr7:136854020-136854170	WERI-Rb-1	eye:	n/a	chr7:136854107-136854128
31	CTCF	chr7:136930382-136930444	LNCaP	prostate:	n/a	n/a
32	CTCF	chr7:136905576-136905648	Lung_OC	lung:	n/a	n/a
33	CTCF	chr7:136972559-136972625	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr7:136854040-136854190	HCM	heart:	n/a	chr7:136854107-136854128
35	CTCF	chr7:136972500-136972650	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr7:136854020-136854170	NHEK	skin:	n/a	chr7:136854107-136854128
37	CTCF	chr7:136972430-136972770	GM12878	blood:	n/a	n/a
38	CTCF	chr7:136854040-136854190	HAc	cerebellar:	n/a	chr7:136854107-136854128
39	CTCF	chr7:136984100-136984250	GM06990	blood:	n/a	n/a
40	CTCF	chr7:136853977-136854248	MCF-7	breast:	n/a	chr7:136854107-136854128
41	CTCF	chr7:136972500-136972650	HMF	breast:	n/a	n/a
42	CTCF	chr7:136854020-136854170	HBMEC	blood vessel:	n/a	chr7:136854107-136854128
43	CTCF	chr7:136972442-136972780	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr7:136972460-136972610	AG04450	lung:	n/a	n/a
45	CTCF	chr7:136854000-136854150	HCM	heart:	n/a	chr7:136854107-136854128
46	CTCF	chr7:136854020-136854170	GM12873	blood:	n/a	chr7:136854107-136854128
47	CTCF	chr7:136853994-136854214	Hela-S3	cervix:	n/a	chr7:136854107-136854128
48	CTCF	chr7:136853980-136854130	MCF-7	breast:	n/a	chr7:136854107-136854128
49	CTCF	chr7:136854080-136854230	K562	blood:	n/a	chr7:136854107-136854128
50	CTCF	chr7:136972460-136972610	AG04449	skin:	n/a	n/a

(count:1164 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:136879401-136879451	ProgFib	skin:	n/a
2	chr7:136944526-136944576	HRCEpiC	kidney:	n/a
3	chr7:136879401-136879451	RPTEC	kidney:	n/a
4	chr7:136928644-136928694	GM12892	blood:	n/a
5	chr7:136845265-136845315	Hepatocyte	liver:	n/a
6	chr7:136879401-136879451	ProgFib	skin:	n/a
7	chr7:136944526-136944576	HRCEpiC	kidney:	n/a
8	chr7:136879401-136879451	RPTEC	kidney:	n/a
9	chr7:136928644-136928694	GM12892	blood:	n/a
10	chr7:136845265-136845315	Hepatocyte	liver:	n/a
11	chr7:136927099-136927149	HAEpiC	amniotic membrane:	n/a
12	chr7:137002261-137002311	PANC-1	pancreas:	n/a
13	chr7:136849317-136849367	HEEpiC	esophagus:	n/a
14	chr7:136849143-136849193	GM12891	blood:	n/a
15	chr7:137002261-137002311	MCF-7	breast:	n/a
16	chr7:136849317-136849367	U87	brain:	n/a
17	chr7:136879401-136879451	NT2-D1	testis:	n/a
18	chr7:136849187-136849237	HMEC	breast:	n/a
19	chr7:136944526-136944576	AG04449	skin:	fetal
20	chr7:136849187-136849237	K562	blood:	n/a
21	chr7:136849143-136849193	CMK	blood:	n/a
22	chr7:136960138-136960188	ProgFib	skin:	n/a
23	chr7:136849317-136849367	A549	lung:	n/a
24	chr7:136845265-136845315	HCF	heart:	n/a
25	chr7:136927099-136927149	LNCaP	prostate:	n/a
26	chr7:136910420-136910470	HEK293	kidney:	embryo
27	chr7:136910420-136910470	GM12892	blood:	n/a
28	chr7:136973838-136973888	PANC-1	pancreas:	n/a
29	chr7:137003665-137003715	SAEC	small airway:	n/a
30	chr7:136849143-136849193	HCF	heart:	n/a
31	chr7:136928644-136928694	HRPEpiC	eye:	n/a
32	chr7:136849187-136849237	H1-hESC	embryonic stem cell:	embryo
33	chr7:136973838-136973888	H1-hESC	embryonic stem cell:	embryo
34	chr7:136973838-136973888	AG09309	skin:	n/a
35	chr7:136960138-136960188	AG09319	gingival:	n/a
36	chr7:136845265-136845315	ProgFib	skin:	n/a
37	chr7:136850736-136850786	SK-N-SH	brain:	n/a
38	chr7:136928644-136928694	SK-N-SH	brain:	n/a
39	chr7:136849187-136849237	HCM	heart:	n/a
40	chr7:136845265-136845315	MCF10A-Er-Src	breast:	n/a
41	chr7:136928644-136928694	AG04450	lung:	fetal
42	chr7:136849187-136849237	NHBE	bronchial:	n/a
43	chr7:136849187-136849237	GM19239	blood:	n/a
44	chr7:136927099-136927149	SKMC	muscle:	n/a
45	chr7:137003665-137003715	AG10803	skin:	n/a
46	chr7:136849018-136849068	AG10803	skin:	n/a
47	chr7:137003665-137003715	AG09319	gingival:	n/a
48	chr7:136849262-136849312	SKMC	muscle:	n/a
49	chr7:136849018-136849068	NB4	blood:	n/a
50	chr7:137002261-137002311	AG09319	gingival:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:136911465..136914095-chr7:136917447..136919624,2	K562	blood:
2	chr7:136915442..136917934-chr7:136955995..136958425,2	K562	blood:
3	chr7:136902230..136905119-chr7:136906745..136908628,2	K562	blood:
4	chr7:136768600..136771525-chr7:136904072..136906566,2	K562	blood:
5	chr7:136939425..136941087-chr7:136941192..136943070,2	K562	blood:
6	chr7:136960021..136961767-chr7:136965044..136967236,2	K562	blood:
7	chr7:136960021..136961767-chr7:136965044..136967236,2	K562	blood:
8	chr7:136930142..136933282-chr7:136935160..136937647,3	K562	blood:
9	chr12:62807018..62807608-chr7:136989360..136989935,2	MCF-7	breast:
10	chr7:136915740..136917893-chr7:136923118..136925670,2	K562	blood:
11	chr7:136854007..136854801-chr7:137137517..137138269,2	MCF-7	breast:
12	chr7:136853835..136854630-chr7:137138677..137139572,6	MCF-7	breast:
13	chr7:136926388..136929879-chr7:136930158..136932908,3	K562	blood:
14	chr7:136926388..136929879-chr7:136930158..136932908,3	K562	blood:
15	chr7:136939425..136941087-chr7:136941192..136943070,2	K562	blood:
16	chr7:136872945..136874531-chr7:136887427..136890361,2	MCF-7	breast:
17	chr7:136858672..136861163-chr7:136864097..136866322,2	K562	blood:
18	chr7:136845496..136847194-chr7:136910849..136912754,2	MCF-7	breast:
19	chr7:136853367..136854657-chr7:137138615..137139665,11	MCF-7	breast:
20	chr7:136853636..136854568-chr7:137022322..137023760,5	MCF-7	breast:
21	chr4:150815194..150816071-chr7:136849876..136850472,2	MCF-7	breast:
22	chr7:136902230..136905119-chr7:136906745..136908628,2	K562	blood:
23	chr20:57132638..57133600-chr7:136910924..136911916,2	MCF-7	breast:
24	chr7:136889214..136890885-chr7:136891240..136892885,2	K562	blood:
25	chr7:136853684..136854424-chr7:137022605..137023178,2	MCF-7	breast:
26	chr7:136853682..136854530-chr7:137276883..137277639,5	MCF-7	breast:
27	chr7:136983518..136985110-chr7:136986061..136988614,2	MCF-7	breast:
28	chr7:136872945..136874531-chr7:136887427..136890361,2	MCF-7	breast:
29	chr7:136911465..136914095-chr7:136917447..136919624,2	K562	blood:
30	chr7:136858672..136861163-chr7:136864097..136866322,2	K562	blood:
31	chr7:136926388..136928401-chr7:136930158..136932908,2	K562	blood:
32	chr7:136845496..136847194-chr7:136910849..136912754,2	MCF-7	breast:
33	chr7:136915740..136917893-chr7:136923118..136925670,2	K562	blood:
34	chr7:136930142..136933282-chr7:136935160..136937647,3	K562	blood:
35	chr7:136853692..136854573-chr7:137276894..137277671,4	MCF-7	breast:
36	chr7:136903773..136906656-chr7:137136989..137139613,2	K562	blood:
37	chr2:196521592..196522296-chr7:136849044..136849880,2	HCT-116	colon:
38	chr7:136926388..136928401-chr7:136930158..136932908,2	K562	blood:
39	chr7:136915442..136917934-chr7:136955995..136958425,2	K562	blood:
40	chr7:136983518..136985110-chr7:136986061..136988614,2	MCF-7	breast:
41	chr7:136889214..136890885-chr7:136891240..136892885,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHRM2-1	chr7:137003339-137003604	ENSG00000231114
2	lnc-PTN-2	chr7:136848868-136849022	ENSG00000234352.5
3	lnc-PTN-4	chr7:136889380-136889587	NONHSAT123576
4	lnc-PTN-2	chr7:136848868-136849017	NONHSAT123574
5	lnc-PTN-2	chr7:136848868-136849088	ENSG00000234352.2
6	lnc-PTN-2	chr7:136866355-136866518	ENSG00000234352
7	lnc-PTN-4	chr7:136888720-136888959	NONHSAT123576
8	lnc-PTN-2	chr7:136848868-136849020	ENSG00000234352.5
9	lnc-PTN-2	chr7:136848868-136849088	ENSG00000234352
10	lnc-PTN-2	chr7:136848868-136849022	ENSG00000234352.5
11	lnc-PTN-2	chr7:136848868-136849017	ENSG00000234352.5
12	lnc-PTN-2	chr7:136848868-136849022	ENSG00000234352.5

No data

Variant related genes	Relation type
ENSG00000231114	TF binding region
ENSG00000224469	TF binding region
ENSG00000234352	TF binding region
ENSG00000202023	TF binding region
ENSG00000231114	CpG island
ENSG00000224469	CpG island
ENSG00000234352	CpG island
ENSG00000202023	CpG island
ENSG00000157680	chromatin interactions
ENSG00000196950	chromatin interactions
MUC17	miRNA target sites
SLC35B4	miRNA target sites

Extended variants
information (count: 5451 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:5451 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372277099	chr7:136831676-136831677	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566690645	chr7:136831718-136831719	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184511617	chr7:136831725-136831726	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553923798	chr7:136831726-136831727	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567239824	chr7:136831752-136831753	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75772893	chr7:136831778-136831779	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs5887822	chr7:136831807-136831808	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35000411	chr7:136831808-136831809	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs11280741	chr7:136831812-136831813	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201155409	chr7:136831813-136831814	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs199788419	chr7:136831815-136831816	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535899785	chr7:136831830-136831831	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556421338	chr7:136831869-136831870	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188865188	chr7:136831895-136831896	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544912569	chr7:136832023-136832024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs141822728	chr7:136832038-136832039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558285114	chr7:136832054-136832055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557498013	chr7:136832101-136832102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143940283	chr7:136832113-136832114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146866116	chr7:136832225-136832226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376609843	chr7:136832262-136832263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs832969	chr7:136832263-136832264	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs373015277	chr7:136832264-136832265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562908068	chr7:136832275-136832276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs140665942	chr7:136832286-136832287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs832968	chr7:136832300-136832301	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs561967025	chr7:136832326-136832327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73727844	chr7:136832334-136832335	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs527924906	chr7:136832335-136832336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs117616459	chr7:136832342-136832343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567297533	chr7:136832356-136832357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547501858	chr7:136832402-136832403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536236685	chr7:136832431-136832432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372605245	chr7:136832438-136832439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs117820396	chr7:136832480-136832481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144372807	chr7:136832482-136832483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540999255	chr7:136832488-136832489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538518182	chr7:136832568-136832569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs151067396	chr7:136832571-136832572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192773182	chr7:136832590-136832591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534552902	chr7:136832591-136832592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs832967	chr7:136832667-136832668	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs184747156	chr7:136832701-136832702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543108297	chr7:136832711-136832712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562709592	chr7:136832737-136832738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576518234	chr7:136832739-136832740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549330718	chr7:136832766-136832767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545703434	chr7:136832773-136832774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189263240	chr7:136832786-136832787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565608020	chr7:136832792-136832793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Neuroticism	17667963	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute myeloid leukemia	17237825	CNVD
Esophageal cancer	21851588	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	21990379	CNVD

Chromatin state (count:941 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136830000-136832000	Enhancers	Muscle Satellite Cultured Cells	--
2	chr7:136830200-136834000	Enhancers	Colon Smooth Muscle	Colon
3	chr7:136830200-136834400	Enhancers	Fetal Heart	heart
4	chr7:136830400-136832400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:136830400-136832400	Enhancers	HSMM	muscle
6	chr7:136830600-136831800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:136830600-136832400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr7:136830600-136833800	Enhancers	Fetal Stomach	stomach
9	chr7:136830800-136833000	Enhancers	HSMMtube	muscle
10	chr7:136830800-136834000	Enhancers	Placenta Amnion	Placenta Amnion
11	chr7:136831000-136831800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:136831000-136832000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:136831000-136833000	Enhancers	Rectal Smooth Muscle	rectum
14	chr7:136831200-136831800	Flanking Active TSS	HMEC	breast
15	chr7:136831200-136831800	Active TSS	NHDF-Ad	bronchial
16	chr7:136831200-136832000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr7:136831200-136832000	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr7:136831200-136832000	Flanking Active TSS	Osteobl	bone
19	chr7:136831400-136831800	Flanking Active TSS	NH-A	brain
20	chr7:136831400-136832200	Enhancers	Brain Germinal Matrix	brain
21	chr7:136831400-136832200	Enhancers	Fetal Kidney	kidney
22	chr7:136831400-136833200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr7:136831600-136831800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr7:136831600-136832000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr7:136831600-136832600	Enhancers	NHLF	lung
26	chr7:136831800-136832000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr7:136831800-136832000	Weak transcription	NHDF-Ad	bronchial
28	chr7:136831800-136832400	Enhancers	HMEC	breast
29	chr7:136831800-136833000	Enhancers	NH-A	brain
30	chr7:136832000-136832200	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr7:136832000-136832400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr7:136832000-136832400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr7:136832000-136832800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr7:136832000-136832800	Enhancers	NHDF-Ad	bronchial
35	chr7:136832000-136832800	Enhancers	Osteobl	bone
36	chr7:136832000-136833800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr7:136832200-136832800	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr7:136832200-136833200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:136832200-136833200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr7:136832200-136835600	Weak transcription	Fetal Kidney	kidney
41	chr7:136832400-136835800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr7:136832600-136833000	Weak transcription	NHLF	lung
43	chr7:136832800-136833000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr7:136832800-136835600	Weak transcription	Osteobl	bone
45	chr7:136833000-136833200	Enhancers	NHLF	lung
46	chr7:136833000-136833600	Weak transcription	Rectal Smooth Muscle	rectum
47	chr7:136833000-136835600	Weak transcription	NH-A	brain
48	chr7:136833000-136838800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr7:136833200-136835200	Weak transcription	NHLF	lung
50	chr7:136833600-136833800	Enhancers	Rectal Smooth Muscle	rectum

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