Variant report

Variant	nsv519151
Chromosome Location	chr7:3413738-3459998
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:448)
CpG islands
(count:61)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:3418058-3418349	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:3419747-3420059	HepG2	liver:	n/a	n/a
3	ATF2	chr7:3439424-3439867	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:3420718-3420741	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr7:3439465-3439755	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr7:3418024-3418475	HepG2	liver:	n/a	n/a
7	CEBPB	chr7:3418069-3418350	HepG2	liver:	n/a	n/a
8	CEBPB	chr7:3443878-3444610	MCF-7	breast:	n/a	n/a
9	CEBPB	chr7:3417979-3418421	HepG2	liver:	n/a	n/a
10	CEBPB	chr7:3427134-3427430	A549	lung:	n/a	chr7:3427395-3427408
11	CEBPB	chr7:3444003-3444489	MCF-7	breast:	n/a	n/a
12	CEBPB	chr7:3420050-3420246	A549	lung:	n/a	n/a
13	CEBPB	chr7:3417057-3417345	HepG2	liver:	n/a	n/a
14	CEBPB	chr7:3457543-3457997	H1-hESC	embryonic stem cell:	n/a	chr7:3457585-3457598 chr7:3457585-3457598
15	CEBPB	chr7:3419990-3420315	HepG2	liver:	n/a	n/a
16	CHD2	chr7:3418316-3418512	HepG2	liver:	n/a	n/a
17	CREB1	chr7:3439466-3439892	H1-hESC	embryonic stem cell:	n/a	n/a
18	CREB1	chr7:3439380-3439963	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr7:3439666-3439828	GM12892	blood:	n/a	n/a
20	CTCF	chr7:3439720-3439870	GM12864	blood:	n/a	n/a
21	CTCF	chr7:3439740-3439771	Fibrobl	skin:	n/a	n/a
22	CTCF	chr7:3439640-3439790	NHDF-neo	bronchial:	n/a	n/a
23	CTCF	chr7:3439543-3439881	A549	lung:	n/a	n/a
24	CTCF	chr7:3439640-3439870	K562	blood:	n/a	n/a
25	CTCF	chr7:3439540-3439690	NHEK	skin:	n/a	n/a
26	CTCF	chr7:3439680-3439830	NB4	blood:	n/a	n/a
27	CTCF	chr7:3439560-3439710	GM12866	blood:	n/a	n/a
28	CTCF	chr7:3439640-3439790	HEK293	kidney:	n/a	n/a
29	CTCF	chr7:3439640-3439790	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr7:3433580-3433730	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr7:3439660-3439810	GM12866	blood:	n/a	n/a
32	CTCF	chr7:3439640-3439790	NHEK	skin:	n/a	n/a
33	CTCF	chr7:3413860-3414010	MCF-7	breast:	n/a	n/a
34	CTCF	chr7:3439660-3439810	GM12873	blood:	n/a	n/a
35	CTCF	chr7:3439620-3439770	HMF	breast:	n/a	n/a
36	CTCF	chr7:3439700-3439850	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr7:3439609-3439860	A549	lung:	n/a	n/a
38	CTCF	chr7:3439580-3439730	BE2_C	brain:	n/a	n/a
39	CTCF	chr7:3419060-3419210	GM12867	blood:	n/a	n/a
40	CTCF	chr7:3439800-3439950	BE2_C	brain:	n/a	n/a
41	CTCF	chr7:3439720-3439870	GM12869	blood:	n/a	n/a
42	CTCF	chr7:3433520-3433670	HCFaa	heart:	n/a	n/a
43	CTCF	chr7:3439580-3439730	GM12869	blood:	n/a	n/a
44	CTCF	chr7:3439660-3439810	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr7:3433539-3433737	GM12878	blood:	n/a	n/a
46	CTCF	chr7:3439880-3440030	GM12873	blood:	n/a	n/a
47	CTCF	chr7:3439643-3439855	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr7:3421860-3422010	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:3418120-3418270	HepG2	liver:	n/a	n/a
50	CTCF	chr7:3433600-3433750	HMEC	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3419305-3419355	BJ	skin:	n/a
2	chr7:3419305-3419355	GM12878	blood:	n/a
3	chr7:3419305-3419355	A549	lung:	n/a
4	chr7:3419305-3419355	Hepatocyte	liver:	n/a
5	chr7:3419305-3419355	AG09309	skin:	n/a
6	chr7:3419305-3419355	NH-A	brain:	n/a
7	chr7:3419305-3419355	SKMC	muscle:	n/a
8	chr7:3419305-3419355	HIPEpiC	eye:	n/a
9	chr7:3419305-3419355	HCT-116	colon:	n/a
10	chr7:3419305-3419355	AG10803	skin:	n/a
11	chr7:3419305-3419355	HEK293	kidney:	embryo
12	chr7:3419305-3419355	HL-60	blood:	n/a
13	chr7:3419305-3419355	PFSK-1	brain:	n/a
14	chr7:3419305-3419355	NHBE	bronchial:	n/a
15	chr7:3419305-3419355	HCM	heart:	n/a
16	chr7:3419305-3419355	ProgFib	skin:	n/a
17	chr7:3419305-3419355	MCF-7	breast:	n/a
18	chr7:3419305-3419355	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:3419305-3419355	ECC-1	luminal epithelium:	n/a
20	chr7:3419305-3419355	HCPEpiC	choroid plexus:	n/a
21	chr7:3419305-3419355	HMEC	breast:	n/a
22	chr7:3419305-3419355	K562	blood:	n/a
23	chr7:3419305-3419355	PANC-1	pancreas:	n/a
24	chr7:3419305-3419355	GM06990	blood:	n/a
25	chr7:3419305-3419355	IMR90	lung:	fetal
26	chr7:3419305-3419355	SK-N-MC	brain:	n/a
27	chr7:3419305-3419355	SAEC	small airway:	n/a
28	chr7:3419305-3419355	NHDF-neo	bronchial:	n/a
29	chr7:3419305-3419355	MCF10A-Er-Src	breast:	n/a
30	chr7:3419305-3419355	H1-hESC	embryonic stem cell:	embryo
31	chr7:3419305-3419355	NT2-D1	testis:	n/a
32	chr7:3419305-3419355	NB4	blood:	n/a
33	chr7:3419305-3419355	HRPEpiC	eye:	n/a
34	chr7:3419305-3419355	HAEpiC	amniotic membrane:	n/a
35	chr7:3419305-3419355	T-47D	breast:	n/a
36	chr7:3419305-3419355	GM19239	blood:	n/a
37	chr7:3419305-3419355	AG04450	lung:	fetal
38	chr7:3419305-3419355	Hela-S3	cervix:	n/a
39	chr7:3419305-3419355	Caco-2	colon:	n/a
40	chr7:3419305-3419355	AG09319	gingival:	n/a
41	chr7:3419305-3419355	CMK	blood:	n/a
42	chr7:3419305-3419355	HRCEpiC	kidney:	n/a
43	chr7:3419305-3419355	HNPCEpiC	eye:	n/a
44	chr7:3419305-3419355	RPTEC	kidney:	n/a
45	chr7:3419305-3419355	HEEpiC	esophagus:	n/a
46	chr7:3419305-3419355	PrEC	prostate:	n/a
47	chr7:3419305-3419355	Jurkat	blood:	n/a
48	chr7:3419305-3419355	LNCaP	prostate:	n/a
49	chr7:3419305-3419355	GM12892	blood:	n/a
50	chr7:3419305-3419355	HUVEC	blood vessel:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:3444047..3446365-chr7:3452049..3455174,3	MCF-7	breast:
2	chr7:3443032..3445719-chr7:3938528..3940389,2	MCF-7	breast:
3	chr7:3435622..3438009-chr7:3442617..3444470,2	MCF-7	breast:
4	chr7:3450055..3452486-chr7:3794915..3797670,2	MCF-7	breast:
5	chr7:3436200..3439462-chr7:3442138..3445077,3	K562	blood:
6	chr7:3425023..3426589-chr7:3427708..3429646,2	MCF-7	breast:
7	chr7:3436200..3438648-chr7:3443337..3445077,2	K562	blood:
8	chr7:3436200..3438648-chr7:3443337..3445077,2	K562	blood:
9	chr7:3441889..3444490-chr7:3452543..3454242,2	MCF-7	breast:
10	chr7:3438230..3440428-chr7:3448766..3450871,2	MCF-7	breast:
11	chr7:3194262..3194922-chr7:3439333..3439841,2	MCF-7	breast:
12	chr7:3419417..3422397-chr7:3422583..3424637,2	K562	blood:
13	chr7:3421160..3422732-chr7:3429225..3430935,2	MCF-7	breast:
14	chr7:3424678..3427459-chr7:3437708..3440654,2	MCF-7	breast:
15	chr7:3425641..3430182-chr7:3430225..3435357,4	MCF-7	breast:
16	chr7:3340063..3340822-chr7:3439252..3440083,5	MCF-7	breast:
17	chr7:3452987..3455737-chr7:3457417..3460056,3	MCF-7	breast:
18	chr7:3444047..3446365-chr7:3452049..3455174,3	MCF-7	breast:
19	chr7:3442245..3445067-chr7:3448256..3450121,2	MCF-7	breast:
20	chr7:3240198..3242825-chr7:3445733..3447901,2	K562	blood:
21	chr7:3419417..3422397-chr7:3422583..3424637,2	K562	blood:
22	chr7:3340385..3341337-chr7:3439295..3440058,3	MCF-7	breast:
23	chr7:3339718..3341766-chr7:3458306..3459954,2	K562	blood:
24	chr7:3444122..3444632-chr7:3471439..3472016,2	MCF-7	breast:
25	chr7:3435622..3438009-chr7:3442617..3444470,2	MCF-7	breast:
26	chr7:3398782..3400855-chr7:3415548..3417886,2	MCF-7	breast:
27	chr7:3427962..3429690-chr7:3438000..3440152,2	K562	blood:
28	chr7:3442245..3445067-chr7:3448256..3450121,2	MCF-7	breast:
29	chr7:3438230..3440428-chr7:3448766..3450871,2	MCF-7	breast:
30	chr7:3348413..3349355-chr7:3439267..3440144,2	MCF-7	breast:
31	chr7:3427962..3429690-chr7:3438000..3440152,2	K562	blood:
32	chr7:3424678..3427459-chr7:3437708..3440654,2	MCF-7	breast:
33	chr7:3425023..3426589-chr7:3427708..3429646,2	MCF-7	breast:
34	chr7:3439202..3440208-chr7:3521793..3522518,3	MCF-7	breast:
35	chr7:3436200..3439462-chr7:3442138..3445077,3	K562	blood:
36	chr7:3421160..3422732-chr7:3429225..3430935,2	MCF-7	breast:
37	chr7:3341947..3342585-chr7:3439297..3440029,2	MCF-7	breast:
38	chr7:3425641..3430182-chr7:3430225..3435357,4	MCF-7	breast:
39	chr7:3441889..3444490-chr7:3452543..3454242,2	MCF-7	breast:
40	chr7:3348530..3349530-chr7:3439336..3440173,5	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000211544	TF binding region
ENSG00000211544	CpG island
ENSG00000211544	chromatin interactions
ENSG00000236708	chromatin interactions
ENSG00000146555	chromatin interactions

Extended variants
information (count: 2450 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2450 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12673513	chr7:3413738-3413739	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115934159	chr7:3413752-3413753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553740913	chr7:3413760-3413761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs79147773	chr7:3413777-3413778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12667184	chr7:3413793-3413794	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs10235815	chr7:3413867-3413868	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs550831342	chr7:3413889-3413890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs146274442	chr7:3413935-3413936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188574630	chr7:3413944-3413945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs117004365	chr7:3413959-3413960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs17813034	chr7:3413987-3413988	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs572169853	chr7:3414016-3414017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs375525722	chr7:3414038-3414039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548469734	chr7:3414044-3414045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116684344	chr7:3414057-3414058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560854658	chr7:3414075-3414076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs138089385	chr7:3414091-3414092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566606589	chr7:3414121-3414122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs534709474	chr7:3414132-3414133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181208431	chr7:3414149-3414150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552918928	chr7:3414154-3414155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539932320	chr7:3414196-3414197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551949300	chr7:3414206-3414207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565077762	chr7:3414223-3414224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186716337	chr7:3414227-3414228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547413611	chr7:3414254-3414255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571433049	chr7:3414261-3414262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567291671	chr7:3414273-3414274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs375880739	chr7:3414293-3414294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs201470214	chr7:3414310-3414311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538731206	chr7:3414322-3414323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557311334	chr7:3414333-3414334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs570236178	chr7:3414337-3414338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370788237	chr7:3414348-3414349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538912409	chr7:3414367-3414368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs559188376	chr7:3414378-3414379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572208566	chr7:3414434-3414435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534685353	chr7:3414435-3414436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs369890164	chr7:3414457-3414458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs78225871	chr7:3414484-3414485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574318469	chr7:3414488-3414489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189122949	chr7:3414494-3414495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs142655679	chr7:3414508-3414509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374741743	chr7:3414519-3414520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144089390	chr7:3414554-3414555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs561584803	chr7:3414573-3414574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs181067204	chr7:3414590-3414591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs369161099	chr7:3414593-3414594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs555742958	chr7:3414617-3414618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10258056	chr7:3414624-3414625	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:82)

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
Pancreatic cancer	17952125	CNVD
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3408800-3426200	Weak transcription	Aorta	Aorta
2	chr7:3410600-3420400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr7:3410800-3415200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:3410800-3420800	Weak transcription	Pancreas	Pancrea
5	chr7:3411800-3420400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:3411800-3420800	Weak transcription	Fetal Brain Male	brain
7	chr7:3412000-3416000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr7:3412000-3416000	Weak transcription	HepG2	liver
9	chr7:3412200-3418800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr7:3412200-3420200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr7:3412400-3413800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr7:3412400-3416800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr7:3412400-3416800	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr7:3412400-3420000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr7:3412400-3420800	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr7:3412400-3420800	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr7:3412800-3416600	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr7:3413000-3414600	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr7:3413000-3418000	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr7:3413800-3414200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr7:3414600-3424200	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr7:3414800-3417000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr7:3415200-3415800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr7:3415800-3416800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr7:3416000-3416200	Enhancers	HepG2	liver
26	chr7:3416000-3417200	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr7:3416200-3416400	Flanking Active TSS	HepG2	liver
28	chr7:3416400-3416800	Enhancers	HepG2	liver
29	chr7:3416600-3417200	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr7:3416800-3417000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr7:3416800-3417200	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr7:3416800-3417200	Flanking Active TSS	HepG2	liver
33	chr7:3416800-3418200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr7:3416800-3419200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr7:3417000-3417200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr7:3417000-3417200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:3417000-3417400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr7:3417000-3418000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr7:3417000-3420800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr7:3417200-3417800	Enhancers	HepG2	liver
41	chr7:3417200-3418200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr7:3417200-3420000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr7:3417200-3420200	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr7:3417400-3420600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr7:3417800-3418600	Flanking Active TSS	HepG2	liver
46	chr7:3418000-3418800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr7:3418000-3419000	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr7:3418000-3419200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:3418200-3419200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:3418200-3420000	Weak transcription	HUES64 Cell Line	embryonic stem cell

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