Variant report

Variant	nsv1032915
Chromosome Location	chr7:3195628-3251756
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:779)
CpG islands
(count:857)
Chromatin interactive
region (count:26)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:779 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:3234233-3234865	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:3221006-3221355	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:3203948-3204296	HepG2	liver:	n/a	n/a
4	ATF2	chr7:3234272-3234806	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:3234177-3234810	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:3240149-3240409	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:3234182-3234735	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr7:3220998-3221446	GM12878	blood:	n/a	n/a
9	BCL3	chr7:3234202-3234797	A549	lung:	n/a	n/a
10	BCL3	chr7:3221093-3221491	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:3216612-3216813	K562	blood:	n/a	n/a
12	CEBPB	chr7:3234205-3234712	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:3234396-3234625	HepG2	liver:	n/a	n/a
14	CEBPB	chr7:3215918-3216112	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr7:3220965-3221379	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:3234300-3234711	A549	lung:	n/a	n/a
17	CEBPB	chr7:3234322-3234665	A549	lung:	n/a	n/a
18	CEBPB	chr7:3231891-3232043	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr7:3221076-3221267	IMR90	lung:	n/a	n/a
20	CEBPB	chr7:3234098-3234698	IMR90	lung:	n/a	n/a
21	CEBPB	chr7:3234374-3234541	K562	blood:	n/a	n/a
22	CEBPB	chr7:3234293-3234711	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr7:3243911-3244232	K562	blood:	n/a	n/a
24	CHD2	chr7:3221032-3221442	HepG2	liver:	n/a	n/a
25	CHD2	chr7:3234357-3234596	HepG2	liver:	n/a	n/a
26	CTBP2	chr7:3234305-3234912	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr7:3202160-3202310	HFF-Myc	foreskin:	n/a	n/a
28	CTCF	chr7:3197360-3197510	HAc	cerebellar:	n/a	n/a
29	CTCF	chr7:3240260-3240410	HCT-116	colon:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341
30	CTCF	chr7:3234340-3234490	SAEC	small airway:	n/a	n/a
31	CTCF	chr7:3202039-3202180	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr7:3201981-3202340	MCF-7	breast:	n/a	chr7:3202038-3202045
33	CTCF	chr7:3202100-3202250	K562	blood:	n/a	n/a
34	CTCF	chr7:3250320-3250470	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr7:3240220-3240370	WERI-Rb-1	eye:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341
36	CTCF	chr7:3239780-3239930	HVMF	connective:	n/a	n/a
37	CTCF	chr7:3240082-3240553	A549	lung:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341
38	CTCF	chr7:3250141-3250635	SK-N-SH	brain:	n/a	n/a
39	CTCF	chr7:3202020-3202170	AoAF	blood vessel:	n/a	chr7:3202038-3202045
40	CTCF	chr7:3250102-3250507	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr7:3240280-3240430	AG10803	skin:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341
42	CTCF	chr7:3202040-3202190	HPF	lung:	n/a	n/a
43	CTCF	chr7:3234320-3234470	HMF	breast:	n/a	n/a
44	CTCF	chr7:3240225-3240433	A549	lung:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341
45	CTCF	chr7:3202033-3202165	Lung_OC	lung:	n/a	chr7:3202038-3202045
46	CTCF	chr7:3234340-3234490	GM12873	blood:	n/a	n/a
47	CTCF	chr7:3240280-3240430	HRE	kidney:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341
48	CTCF	chr7:3250081-3250544	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:3240240-3240390	HPF	lung:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341
50	CTCF	chr7:3234300-3234450	AG04450	lung:	n/a	n/a

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3208493-3208543	GM12891	blood:	n/a
2	chr7:3215543-3215593	A549	lung:	n/a
3	chr7:3215543-3215593	AG04449	skin:	fetal
4	chr7:3208493-3208543	GM12891	blood:	n/a
5	chr7:3215543-3215593	A549	lung:	n/a
6	chr7:3215543-3215593	AG04449	skin:	fetal
7	chr7:3221150-3221200	Jurkat	blood:	n/a
8	chr7:3215287-3215337	Hela-S3	cervix:	n/a
9	chr7:3215287-3215337	HL-60	blood:	n/a
10	chr7:3215543-3215593	HRCEpiC	kidney:	n/a
11	chr7:3215543-3215593	SAEC	small airway:	n/a
12	chr7:3221150-3221200	HRE	kidney:	n/a
13	chr7:3227332-3227382	NT2-D1	testis:	n/a
14	chr7:3221150-3221200	HMEC	breast:	n/a
15	chr7:3221373-3221423	HNPCEpiC	eye:	n/a
16	chr7:3227332-3227382	ProgFib	skin:	n/a
17	chr7:3227277-3227327	HAEpiC	amniotic membrane:	n/a
18	chr7:3215287-3215337	Jurkat	blood:	n/a
19	chr7:3234697-3234747	HEEpiC	esophagus:	n/a
20	chr7:3215287-3215337	NH-A	brain:	n/a
21	chr7:3221373-3221423	AG09319	gingival:	n/a
22	chr7:3227332-3227382	RPTEC	kidney:	n/a
23	chr7:3214289-3214339	K562	blood:	n/a
24	chr7:3221228-3221278	RPTEC	kidney:	n/a
25	chr7:3215287-3215337	Hepatocyte	liver:	n/a
26	chr7:3234697-3234747	AG04449	skin:	fetal
27	chr7:3227277-3227327	HepG2	liver:	n/a
28	chr7:3227277-3227327	Hepatocyte	liver:	n/a
29	chr7:3221373-3221423	HMEC	breast:	n/a
30	chr7:3221228-3221278	HL-60	blood:	n/a
31	chr7:3207719-3207769	HPAEpiC	pulmonary alveolar:	n/a
32	chr7:3214289-3214339	ProgFib	skin:	n/a
33	chr7:3221228-3221278	HepG2	liver:	n/a
34	chr7:3227262-3227312	K562	blood:	n/a
35	chr7:3215287-3215337	HNPCEpiC	eye:	n/a
36	chr7:3234697-3234747	HAEpiC	amniotic membrane:	n/a
37	chr7:3234697-3234747	SKMC	muscle:	n/a
38	chr7:3208793-3208843	GM06990	blood:	n/a
39	chr7:3227277-3227327	NT2-D1	testis:	n/a
40	chr7:3207719-3207769	MCF10A-Er-Src	breast:	n/a
41	chr7:3214289-3214339	ECC-1	luminal epithelium:	n/a
42	chr7:3214400-3214450	GM12878	blood:	n/a
43	chr7:3214400-3214450	Jurkat	blood:	n/a
44	chr7:3221373-3221423	HRE	kidney:	n/a
45	chr7:3208493-3208543	AG04450	lung:	fetal
46	chr7:3215287-3215337	BJ	skin:	n/a
47	chr7:3227262-3227312	IMR90	lung:	fetal
48	chr7:3215543-3215593	U87	brain:	n/a
49	chr7:3227332-3227382	NHDF-neo	bronchial:	n/a
50	chr7:3215287-3215337	NHBE	bronchial:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:3210617..3212945-chr7:3214732..3216839,2	K562	blood:
2	chr7:3128837..3129871-chr7:3239803..3240577,4	MCF-7	breast:
3	chr7:3201417..3202351-chr7:3240242..3240878,3	MCF-7	breast:
4	chr7:2914055..2915867-chr7:3204506..3206043,2	MCF-7	breast:
5	chr7:3249846..3250536-chr7:3341685..3342449,3	MCF-7	breast:
6	chr7:3201417..3202351-chr7:3240242..3240878,3	MCF-7	breast:
7	chr7:3210592..3212478-chr7:3220599..3222530,2	K562	blood:
8	chr7:3210592..3212478-chr7:3220599..3222530,2	K562	blood:
9	chr7:3198032..3200716-chr7:3210631..3213455,2	MCF-7	breast:
10	chr7:2925307..2926930-chr7:3193219..3196331,3	MCF-7	breast:
11	chr7:2926533..2927268-chr7:3239915..3240463,3	MCF-7	breast:
12	chr7:3227729..3230209-chr7:3232264..3234725,2	MCF-7	breast:
13	chr7:3210617..3212945-chr7:3214732..3216839,2	K562	blood:
14	chr7:2915975..2917721-chr7:3231286..3232804,2	MCF-7	breast:
15	chr7:3251471..3253553-chr7:3281258..3284246,2	MCF-7	breast:
16	chr7:2912750..2915143-chr7:3228683..3231010,3	MCF-7	breast:
17	chr7:2913057..2915172-chr7:3198284..3201204,2	MCF-7	breast:
18	chr7:3240198..3242825-chr7:3445733..3447901,2	K562	blood:
19	chr7:3250247..3250807-chr7:3340190..3341077,3	MCF-7	breast:
20	chr7:2926249..2926927-chr7:3240062..3240775,2	MCF-7	breast:
21	chr7:3210553..3212945-chr7:3214110..3216839,3	K562	blood:
22	chr7:2921568..2923869-chr7:3228214..3231115,2	MCF-7	breast:
23	chr7:3227729..3230209-chr7:3232264..3234725,2	MCF-7	breast:
24	chr7:3104998..3105685-chr7:3239854..3240733,2	MCF-7	breast:
25	chr7:3205607..3207977-chr7:3220687..3223407,2	K562	blood:
26	chr7:3205607..3207977-chr7:3220687..3223407,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC091801.1.1-2	chr7:3234354-3234428	XLOC_006340
2	lnc-AC091801.1.1-1	chr7:3205664-3205764	XLOC_006339
3	lnc-CARD11-4	chr7:3204171-3204221	NONHSAT118845
4	lnc-CARD11-4	chr7:3204353-3204414	NONHSAT118845
5	lnc-AC091801.1.1-4	chr7:3242576-3242787	XLOC_006342
6	lnc-AC091801.1.1-1	chr7:3197771-3197888	XLOC_006339
7	lnc-AC091801.1.1-1	chr7:3214230-3214287	NONHSAT118844
8	lnc-AC091801.1.1-1	chr7:3205664-3205764	NONHSAT118844
9	lnc-AC091801.1.1-2	chr7:3233737-3234256	XLOC_006340
10	lnc-AC091801.1.1-1	chr7:3214230-3214287	XLOC_006339
11	lnc-AC091801.1.1-4	chr7:3243575-3243666	XLOC_006342
12	lnc-CARD11-4	chr7:3202784-3203088	NONHSAT118845
13	lnc-AC091801.1.1-1	chr7:3197771-3197975	XLOC_006339

No data

Variant related genes	Relation type
ENSG00000217455	TF binding region
ENSG00000231892	TF binding region
ENSG00000217455	CpG island
ENSG00000231892	CpG island
ENSG00000217455	chromatin interactions
ENSG00000236708	chromatin interactions
HIPK3	miRNA target sites

Extended variants
information (count: 3203 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:3203 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13228485	chr7:3195628-3195629	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560390474	chr7:3195635-3195636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577623831	chr7:3195638-3195639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570655102	chr7:3195665-3195666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs139874643	chr7:3195667-3195668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189769190	chr7:3195681-3195682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs6949265	chr7:3195727-3195728	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs575437916	chr7:3195789-3195790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116821840	chr7:3195790-3195791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557934911	chr7:3195797-3195798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577931399	chr7:3195833-3195834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546288443	chr7:3195885-3195886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181466034	chr7:3195902-3195903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186035366	chr7:3195949-3195950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372573108	chr7:3195955-3195956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs4599715	chr7:3196005-3196006	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs529317171	chr7:3196049-3196050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs4535632	chr7:3196055-3196056	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs117291674	chr7:3196085-3196086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2396954	chr7:3196117-3196118	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs564313394	chr7:3196132-3196133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533333299	chr7:3196135-3196136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546818846	chr7:3196173-3196174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566224923	chr7:3196216-3196217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535576209	chr7:3196222-3196223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534540123	chr7:3196234-3196235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190807944	chr7:3196256-3196257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568836493	chr7:3196261-3196262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540090306	chr7:3196309-3196310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560004896	chr7:3196318-3196319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs1074119	chr7:3196333-3196334	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs2396953	chr7:3196369-3196370	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs578027225	chr7:3196387-3196388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533955963	chr7:3196424-3196425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1074118	chr7:3196435-3196436	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs573248020	chr7:3196449-3196450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552716694	chr7:3196466-3196467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531541052	chr7:3196475-3196476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150719884	chr7:3196488-3196489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183209724	chr7:3196546-3196547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536267706	chr7:3196593-3196594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544233275	chr7:3196596-3196597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186501327	chr7:3196610-3196611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs75913433	chr7:3196611-3196612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540417140	chr7:3196647-3196648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs9791708	chr7:3196656-3196657	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs11766372	chr7:3196703-3196704	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs559237569	chr7:3196730-3196731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190496617	chr7:3196763-3196764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555695043	chr7:3196777-3196778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
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
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:406 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3178400-3204600	Weak transcription	Right Atrium	heart
2	chr7:3191600-3197200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr7:3192200-3197200	Weak transcription	Primary B cells from cord blood	blood
4	chr7:3192600-3196800	Weak transcription	Primary B cells from peripheral blood	blood
5	chr7:3193600-3197000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr7:3196800-3197600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr7:3196800-3197600	Enhancers	Primary B cells from peripheral blood	blood
8	chr7:3197000-3197200	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
9	chr7:3197000-3197400	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr7:3197000-3197600	Enhancers	Esophagus	oesophagus
11	chr7:3197000-3197800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
12	chr7:3197000-3197800	Enhancers	H1 Cell Line	embryonic stem cell
13	chr7:3197000-3197800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr7:3197000-3198200	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr7:3197200-3197400	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr7:3197200-3197600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr7:3197200-3197600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr7:3197200-3197600	Bivalent Enhancer	Fetal Muscle Leg	muscle
19	chr7:3197200-3197800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr7:3197200-3197800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr7:3197200-3197800	Enhancers	Primary B cells from cord blood	blood
22	chr7:3197200-3197800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr7:3197200-3197800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr7:3197200-3197800	Enhancers	NH-A	brain
25	chr7:3197400-3198800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr7:3197600-3197800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr7:3197600-3197800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr7:3197600-3197800	Flanking Active TSS	Esophagus	oesophagus
29	chr7:3197600-3197800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
30	chr7:3197600-3197800	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
31	chr7:3197600-3198000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr7:3197600-3198000	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr7:3197600-3198000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
34	chr7:3197600-3198000	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
35	chr7:3197600-3198000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
36	chr7:3197600-3198200	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr7:3197600-3198600	Bivalent Enhancer	Adipose Nuclei	Adipose
38	chr7:3197800-3198000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
39	chr7:3197800-3199200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr7:3197800-3207000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr7:3198000-3198200	Active TSS	Fetal Muscle Leg	muscle
42	chr7:3198000-3198400	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
43	chr7:3198200-3199000	Enhancers	Fetal Muscle Leg	muscle
44	chr7:3198400-3198600	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
45	chr7:3198800-3199200	Enhancers	Fetal Kidney	kidney
46	chr7:3198800-3201400	Enhancers	Pancreas	Pancrea
47	chr7:3199200-3200600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr7:3201000-3201200	Enhancers	Gastric	stomach
49	chr7:3201200-3203000	Weak transcription	Gastric	stomach
50	chr7:3201400-3202800	Weak transcription	Pancreas	Pancrea

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