Variant report

Variant	nsv888680
Chromosome Location	chr7:87065687-87101407
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:371)
CpG islands
(count:62)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:371 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:87093353-87093783	HepG2	liver:	n/a	n/a
2	ATF1	chr7:87068362-87068484	K562	blood:	n/a	n/a
3	ATF1	chr7:87080871-87080985	K562	blood:	n/a	n/a
4	ATF2	chr7:87075193-87075772	GM12878	blood:	n/a	n/a
5	ATF2	chr7:87075213-87075701	GM12878	blood:	n/a	n/a
6	BACH1	chr7:87094518-87094660	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr7:87075232-87075613	GM12878	blood:	n/a	n/a
8	BCL11A	chr7:87075212-87075653	GM12878	blood:	n/a	chr7:87075396-87075405
9	BCL11A	chr7:87075188-87075625	GM12878	blood:	n/a	chr7:87075396-87075405
10	BHLHE40	chr7:87075261-87075645	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:87093399-87093797	HepG2	liver:	n/a	n/a
12	BRCA1	chr7:87093351-87093701	HepG2	liver:	n/a	n/a
13	CCNT2	chr7:87089363-87089563	K562	blood:	n/a	n/a
14	CEBPB	chr7:87077625-87077807	HepG2	liver:	n/a	chr7:87077714-87077727
15	CEBPB	chr7:87093392-87093696	HepG2	liver:	n/a	n/a
16	CEBPD	chr7:87094462-87094862	HepG2	liver:	n/a	n/a
17	CHD2	chr7:87075152-87075611	GM12878	blood:	n/a	n/a
18	CHD2	chr7:87093418-87093639	HepG2	liver:	n/a	n/a
19	CHD2	chr7:87094469-87094656	HepG2	liver:	n/a	n/a
20	CHD2	chr7:87088175-87088219	K562	blood:	n/a	n/a
21	CHD2	chr7:87094526-87094716	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr7:87075045-87075699	GM12878	blood:	n/a	n/a
23	CTCF	chr7:87081740-87081890	NHLF	lung:	n/a	n/a
24	CTCF	chr7:87081620-87081770	HMF	breast:	n/a	n/a
25	CTCF	chr7:87077740-87077890	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr7:87081740-87081890	HA-sp	spinal cord:	n/a	n/a
27	CTCF	chr7:87081712-87081869	MCF-7	breast:	n/a	n/a
28	CTCF	chr7:87081724-87081860	HepG2	liver:	n/a	n/a
29	CTCF	chr7:87081725-87081843	K562	blood:	n/a	n/a
30	CTCF	chr7:87081449-87082122	A549	lung:	n/a	n/a
31	CTCF	chr7:87081780-87081930	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr7:87081634-87081927	K562	blood:	n/a	n/a
33	CTCF	chr7:87081600-87081750	HAc	cerebellar:	n/a	n/a
34	CTCF	chr7:87094620-87094770	SAEC	small airway:	n/a	n/a
35	CTCF	chr7:87081700-87081850	HepG2	liver:	n/a	n/a
36	CTCF	chr7:87081800-87081950	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr7:87081740-87081890	MCF-7	breast:	n/a	n/a
38	CTCF	chr7:87094675-87094813	MCF-7	breast:	n/a	n/a
39	CTCF	chr7:87081760-87081910	Caco-2	colon:	n/a	n/a
40	CTCF	chr7:87094773-87094787	HepG2	liver:	n/a	n/a
41	CTCF	chr7:87094680-87094830	Caco-2	colon:	n/a	n/a
42	CTCF	chr7:87094620-87094770	HepG2	liver:	n/a	n/a
43	CTCF	chr7:87081720-87081870	AG10803	skin:	n/a	n/a
44	CTCF	chr7:87081728-87081848	Gliobla	brain:	n/a	n/a
45	CTCF	chr7:87081720-87081870	RPTEC	kidney:	n/a	n/a
46	CTCF	chr7:87081780-87081930	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr7:87081727-87081882	GM12878	blood:	n/a	n/a
48	CTCF	chr7:87081721-87081874	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr7:87094720-87094870	HEK293	kidney:	n/a	n/a
50	CTCF	chr7:87081700-87081850	BE2_C	brain:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:87093634-87093684	ECC-1	luminal epithelium:	n/a
2	chr7:87093634-87093684	ECC-1	luminal epithelium:	n/a
3	chr7:87093634-87093684	HNPCEpiC	eye:	n/a
4	chr7:87093634-87093684	PANC-1	pancreas:	n/a
5	chr7:87093634-87093684	SAEC	small airway:	n/a
6	chr7:87093634-87093684	A549	lung:	n/a
7	chr7:87093634-87093684	HepG2	liver:	n/a
8	chr7:87093634-87093684	BE2_C	brain:	n/a
9	chr7:87093634-87093684	ProgFib	skin:	n/a
10	chr7:87093634-87093684	HMEC	breast:	n/a
11	chr7:87093634-87093684	NH-A	brain:	n/a
12	chr7:87093634-87093684	Hepatocyte	liver:	n/a
13	chr7:87093634-87093684	HEK293	kidney:	embryo
14	chr7:87093634-87093684	H1-hESC	embryonic stem cell:	embryo
15	chr7:87093634-87093684	AG04449	skin:	fetal
16	chr7:87093634-87093684	GM06990	blood:	n/a
17	chr7:87093634-87093684	AoSMC	blood vessel:	n/a
18	chr7:87093634-87093684	AG04450	lung:	fetal
19	chr7:87093634-87093684	U87	brain:	n/a
20	chr7:87093634-87093684	HUVEC	blood vessel:	n/a
21	chr7:87093634-87093684	SK-N-MC	brain:	n/a
22	chr7:87093634-87093684	HIPEpiC	eye:	n/a
23	chr7:87093634-87093684	GM12892	blood:	n/a
24	chr7:87093634-87093684	CMK	blood:	n/a
25	chr7:87093634-87093684	HRCEpiC	kidney:	n/a
26	chr7:87093634-87093684	HL-60	blood:	n/a
27	chr7:87093634-87093684	K562	blood:	n/a
28	chr7:87093634-87093684	Jurkat	blood:	n/a
29	chr7:87093634-87093684	RPTEC	kidney:	n/a
30	chr7:87093634-87093684	HAEpiC	amniotic membrane:	n/a
31	chr7:87093634-87093684	AG09319	gingival:	n/a
32	chr7:87093634-87093684	HEEpiC	esophagus:	n/a
33	chr7:87093634-87093684	T-47D	breast:	n/a
34	chr7:87093634-87093684	ovcar-3	ovarian:	n/a
35	chr7:87093634-87093684	AG09309	skin:	n/a
36	chr7:87093634-87093684	PFSK-1	brain:	n/a
37	chr7:87093634-87093684	BJ	skin:	n/a
38	chr7:87093634-87093684	HCF	heart:	n/a
39	chr7:87093634-87093684	NT2-D1	testis:	n/a
40	chr7:87093634-87093684	MCF10A-Er-Src	breast:	n/a
41	chr7:87093634-87093684	MCF-7	breast:	n/a
42	chr7:87093634-87093684	PrEC	prostate:	n/a
43	chr7:87093634-87093684	NB4	blood:	n/a
44	chr7:87093634-87093684	HRE	kidney:	n/a
45	chr7:87093634-87093684	GM12891	blood:	n/a
46	chr7:87093634-87093684	GM19239	blood:	n/a
47	chr7:87093634-87093684	HCPEpiC	choroid plexus:	n/a
48	chr7:87093634-87093684	IMR90	lung:	fetal
49	chr7:87093634-87093684	LNCaP	prostate:	n/a
50	chr7:87093634-87093684	NHDF-neo	bronchial:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:86568193..86568776-chr7:87081301..87082150,2	MCF-7	breast:
2	chr7:87060366..87063144-chr7:87081442..87083012,2	MCF-7	breast:
3	chr7:87075903..87078103-chr7:87080060..87082449,2	K562	blood:
4	chr7:87075903..87078103-chr7:87080060..87082449,2	K562	blood:
5	chr7:87064330..87066764-chr7:87067722..87070554,3	K562	blood:
6	chr7:87064944..87067466-chr7:87067483..87069471,2	MCF-7	breast:
7	chr7:87064330..87066764-chr7:87067722..87070554,3	K562	blood:
8	chr7:86848248..86850327-chr7:87074296..87076315,2	MCF-7	breast:
9	chr7:87073633..87076529-chr7:87078114..87081650,4	K562	blood:
10	chr7:87043780..87045715-chr7:87084104..87086345,2	MCF-7	breast:
11	chr7:87064944..87067466-chr7:87067483..87069471,2	MCF-7	breast:
12	chr7:86972942..86975537-chr7:87069538..87072015,2	MCF-7	breast:
13	chr7:87073633..87076529-chr7:87078114..87081650,4	K562	blood:
14	chr7:87051942..87054838-chr7:87071863..87073802,2	K562	blood:

No data

Variant related genes	Relation type
ABCB4	TF binding region
ABCB4	CpG island
ENSG00000182165	chromatin interactions
ENSG00000005469	chromatin interactions
ENSG00000135185	chromatin interactions
ENSG00000005471	chromatin interactions

Extended variants
information (count: 1307 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1307 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17651890	chr7:87065687-87065688	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183255041	chr7:87065713-87065714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564760706	chr7:87065839-87065840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs45567342	chr7:87065899-87065900	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs45464493	chr7:87065909-87065910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567937055	chr7:87065975-87065976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535446659	chr7:87065978-87065979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547048418	chr7:87065998-87065999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs113718619	chr7:87066001-87066002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs386715515	chr7:87066002-87066003	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs565440227	chr7:87066003-87066004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539245166	chr7:87066014-87066015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538625475	chr7:87066016-87066017	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs116874664	chr7:87066067-87066068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs144450850	chr7:87066074-87066075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555654689	chr7:87066102-87066103	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574704272	chr7:87066125-87066126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370835446	chr7:87066137-87066138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191465024	chr7:87066164-87066165	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183664359	chr7:87066214-87066215	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs45503696	chr7:87066230-87066231	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs532444224	chr7:87066281-87066282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546404895	chr7:87066309-87066310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146593198	chr7:87066347-87066348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374543317	chr7:87066425-87066426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187977253	chr7:87066435-87066436	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543143171	chr7:87066446-87066447	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550171657	chr7:87066460-87066461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs140187627	chr7:87066482-87066483	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528835503	chr7:87066552-87066553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547036251	chr7:87066564-87066565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs45547643	chr7:87066585-87066586	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs45481793	chr7:87066589-87066590	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs193230770	chr7:87066641-87066642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs45527836	chr7:87066678-87066679	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs45622838	chr7:87066703-87066704	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs550434833	chr7:87066760-87066761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs151254447	chr7:87066769-87066770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573925655	chr7:87066780-87066781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs45488793	chr7:87066792-87066793	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs190208068	chr7:87066814-87066815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192799398	chr7:87066822-87066823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546292926	chr7:87066826-87066827	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs45563433	chr7:87066830-87066831	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs201059673	chr7:87066834-87066835	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs45575433	chr7:87066837-87066838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34415428	chr7:87066854-87066855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs45552540	chr7:87066903-87066904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562238076	chr7:87066908-87066909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573435909	chr7:87066911-87066912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	16616336	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:213 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:86980000-87085600	Weak transcription	Right Ventricle	heart
2	chr7:87019800-87079400	Strong transcription	Liver	Liver
3	chr7:87024800-87093200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr7:87040800-87072400	Weak transcription	Aorta	Aorta
5	chr7:87040800-87085600	Weak transcription	Psoas Muscle	Psoas
6	chr7:87047000-87078000	Strong transcription	Primary B cells from cord blood	blood
7	chr7:87051200-87085600	Weak transcription	Fetal Heart	heart
8	chr7:87052200-87072000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr7:87055800-87075000	Weak transcription	GM12878-XiMat	blood
10	chr7:87056200-87075200	Strong transcription	Primary B cells from peripheral blood	blood
11	chr7:87061000-87066200	Weak transcription	Left Ventricle	heart
12	chr7:87062200-87070400	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr7:87064000-87069200	Strong transcription	Skeletal Muscle Female	skeletal muscle
14	chr7:87064600-87077800	Weak transcription	Spleen	Spleen
15	chr7:87064800-87066800	Strong transcription	HepG2	liver
16	chr7:87065000-87077800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr7:87065200-87067600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr7:87065200-87068000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:87066200-87066800	Strong transcription	Left Ventricle	heart
20	chr7:87066800-87072000	Weak transcription	HepG2	liver
21	chr7:87066800-87085600	Weak transcription	Left Ventricle	heart
22	chr7:87068000-87069400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr7:87068800-87069200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr7:87068800-87069200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr7:87069000-87069600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr7:87069200-87071800	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr7:87069400-87071800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr7:87070400-87072800	Strong transcription	Skeletal Muscle Male	skeletal muscle
29	chr7:87071800-87072800	Strong transcription	Skeletal Muscle Female	skeletal muscle
30	chr7:87071800-87073200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr7:87072000-87073800	Strong transcription	HepG2	liver
32	chr7:87072400-87072800	Genic enhancers	Aorta	Aorta
33	chr7:87072600-87073600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:87072800-87077800	Weak transcription	Aorta	Aorta
35	chr7:87072800-87079000	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr7:87072800-87079200	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr7:87073200-87087000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr7:87073800-87076400	Weak transcription	HepG2	liver
39	chr7:87074200-87074600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr7:87074600-87079000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr7:87075000-87075600	Enhancers	GM12878-XiMat	blood
42	chr7:87075200-87075600	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr7:87075200-87075600	Genic enhancers	Primary B cells from peripheral blood	blood
44	chr7:87075600-87081800	Weak transcription	GM12878-XiMat	blood
45	chr7:87075600-87094800	Strong transcription	Primary B cells from peripheral blood	blood
46	chr7:87076400-87081600	Strong transcription	HepG2	liver
47	chr7:87076600-87077000	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr7:87076800-87077200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr7:87077000-87078400	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr7:87077600-87078000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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