Variant report

Variant	nsv818476
Chromosome Location	chr7:7774684-7779324
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:51)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:51 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr7:7778842-7779627	GM12878	blood:	n/a	n/a
2	CHD2	chr7:7778844-7779662	GM12878	blood:	n/a	n/a
3	CTCF	chr7:7778340-7778490	HAc	cerebellar:	n/a	n/a
4	CUX1	chr7:7778723-7779439	GM12878	blood:	n/a	n/a
5	E2F4	chr7:7774811-7774838	MCF10A-Er-Src	breast:	n/a	n/a
6	EBF1	chr7:7775600-7775884	GM12878	blood:	n/a	chr7:7775746-7775759 chr7:7775747-7775758
7	EBF1	chr7:7775605-7775854	GM12878	blood:	n/a	chr7:7775746-7775759 chr7:7775747-7775758
8	EBF1	chr7:7778808-7779214	GM12878	blood:	n/a	n/a
9	EP300	chr7:7778428-7778554	GM12878	blood:	n/a	n/a
10	EP300	chr7:7778798-7779306	GM12878	blood:	n/a	n/a
11	EP300	chr7:7778754-7779623	GM12878	blood:	n/a	n/a
12	EP300	chr7:7778813-7779277	GM12878	blood:	n/a	n/a
13	EP300	chr7:7778926-7779316	HepG2	liver:	n/a	n/a
14	FOXA1	chr7:7778890-7779331	HepG2	liver:	n/a	n/a
15	FOXA1	chr7:7778940-7779239	HepG2	liver:	n/a	n/a
16	FOXA1	chr7:7778945-7779351	HepG2	liver:	n/a	n/a
17	GATA3	chr7:7777126-7777765	A549	lung:	n/a	n/a
18	GATA3	chr7:7777211-7777808	MCF-7	breast:	n/a	n/a
19	GATA3	chr7:7776994-7777944	MCF-7	breast:	n/a	n/a
20	GATA3	chr7:7777357-7777638	T-47D	breast:	n/a	n/a
21	GTF2F1	chr7:7775982-7776007	H1-hESC	embryonic stem cell:	n/a	n/a
22	IKZF1	chr7:7779042-7779235	GM12878	blood:	n/a	n/a
23	MAFK	chr7:7778730-7779028	HepG2	liver:	n/a	chr7:7778865-7778885 chr7:7778868-7778882 chr7:7778867-7778883
24	MAX	chr7:7778420-7778617	GM12878	blood:	n/a	n/a
25	MEF2A	chr7:7778841-7779339	GM12878	blood:	n/a	chr7:7779151-7779166 chr7:7779176-7779197 chr7:7778953-7778974 chr7:7779181-7779195 chr7:7779176-7779197
26	MEF2A	chr7:7778898-7779420	GM12878	blood:	n/a	chr7:7779151-7779166 chr7:7779176-7779197 chr7:7778953-7778974 chr7:7779181-7779195 chr7:7779360-7779375 chr7:7779176-7779197
27	MEF2C	chr7:7778872-7779427	GM12878	blood:	n/a	chr7:7779151-7779166 chr7:7779176-7779197 chr7:7779179-7779194 chr7:7778953-7778974 chr7:7779181-7779195 chr7:7779360-7779375 chr7:7779176-7779197
28	MXI1	chr7:7778904-7779762	GM12878	blood:	n/a	n/a
29	MYC	chr7:7778402-7778419	MCF-7	breast:	n/a	n/a
30	NFE2	chr7:7775611-7775612	GM12878	blood:	n/a	n/a
31	NFIC	chr7:7778819-7779435	GM12878	blood:	n/a	n/a
32	NFIC	chr7:7778932-7779466	HepG2	liver:	n/a	n/a
33	NR2F2	chr7:7778833-7779496	HepG2	liver:	n/a	n/a
34	NR2F2	chr7:7778863-7779427	MCF-7	breast:	n/a	n/a
35	POLR2A	chr7:7778504-7778512	Gliobla	brain:	n/a	n/a
36	POLR2A	chr7:7776306-7776665	H1-neurons	neurons:	n/a	n/a
37	POLR2A	chr7:7776267-7776716	H1-neurons	neurons:	n/a	n/a
38	POLR2A	chr7:7776314-7776320	GM12878	blood:	n/a	n/a
39	POLR2A	chr7:7777454-7777512	MCF10A-Er-Src	breast:	n/a	n/a
40	RCOR1	chr7:7778069-7778123	GM12878	blood:	n/a	n/a
41	RCOR1	chr7:7778581-7779271	GM12878	blood:	n/a	n/a
42	RCOR1	chr7:7778543-7778564	HepG2	liver:	n/a	n/a
43	RUNX3	chr7:7778926-7779246	GM12878	blood:	n/a	n/a
44	RUNX3	chr7:7778747-7779410	GM12878	blood:	n/a	n/a
45	SIN3A	chr7:7776323-7776628	H1-hESC	embryonic stem cell:	n/a	n/a
46	STAT1	chr7:7778561-7778737	GM12878	blood:	n/a	n/a
47	TBL1XR1	chr7:7778827-7779419	GM12878	blood:	n/a	n/a
48	TCF7L2	chr7:7777914-7778230	PANC-1	pancreas:	n/a	n/a
49	TCF7L2	chr7:7778778-7779135	HepG2	liver:	n/a	n/a
50	TCF7L2	chr7:7777259-7777650	PANC-1	pancreas:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:7776115-7776165	AG09309	skin:	n/a
2	chr7:7776115-7776165	CMK	blood:	n/a
3	chr7:7776115-7776165	PFSK-1	brain:	n/a
4	chr7:7776115-7776165	GM12892	blood:	n/a
5	chr7:7776115-7776165	A549	lung:	n/a
6	chr7:7776115-7776165	Caco-2	colon:	n/a
7	chr7:7776115-7776165	HRPEpiC	eye:	n/a
8	chr7:7776115-7776165	Hepatocyte	liver:	n/a
9	chr7:7776115-7776165	NT2-D1	testis:	n/a
10	chr7:7776115-7776165	SKMC	muscle:	n/a
11	chr7:7776115-7776165	HAEpiC	amniotic membrane:	n/a
12	chr7:7776115-7776165	K562	blood:	n/a
13	chr7:7776115-7776165	AG10803	skin:	n/a
14	chr7:7776115-7776165	HRE	kidney:	n/a
15	chr7:7776115-7776165	SK-N-SH_RA	brain:	n/a
16	chr7:7776115-7776165	HNPCEpiC	eye:	n/a
17	chr7:7776115-7776165	PrEC	prostate:	n/a
18	chr7:7776115-7776165	HL-60	blood:	n/a
19	chr7:7776115-7776165	NB4	blood:	n/a
20	chr7:7776115-7776165	HCPEpiC	choroid plexus:	n/a
21	chr7:7776115-7776165	NHDF-neo	bronchial:	n/a
22	chr7:7776115-7776165	HCM	heart:	n/a
23	chr7:7776115-7776165	MCF-7	breast:	n/a
24	chr7:7776115-7776165	ECC-1	luminal epithelium:	n/a
25	chr7:7776115-7776165	HIPEpiC	eye:	n/a
26	chr7:7776115-7776165	NH-A	brain:	n/a
27	chr7:7776115-7776165	T-47D	breast:	n/a
28	chr7:7776115-7776165	LNCaP	prostate:	n/a
29	chr7:7776115-7776165	H1-hESC	embryonic stem cell:	embryo
30	chr7:7776115-7776165	HCF	heart:	n/a
31	chr7:7776115-7776165	HepG2	liver:	n/a
32	chr7:7776115-7776165	Hela-S3	cervix:	n/a
33	chr7:7776115-7776165	HCT-116	colon:	n/a
34	chr7:7776115-7776165	HEK293	kidney:	embryo
35	chr7:7776115-7776165	AoSMC	blood vessel:	n/a
36	chr7:7776115-7776165	AG04449	skin:	fetal
37	chr7:7776115-7776165	BJ	skin:	n/a
38	chr7:7776115-7776165	HMEC	breast:	n/a
39	chr7:7776115-7776165	SK-N-MC	brain:	n/a
40	chr7:7776115-7776165	MCF10A-Er-Src	breast:	n/a
41	chr7:7776115-7776165	BE2_C	brain:	n/a
42	chr7:7776115-7776165	AG09319	gingival:	n/a
43	chr7:7776115-7776165	Jurkat	blood:	n/a
44	chr7:7776115-7776165	U87	brain:	n/a
45	chr7:7776115-7776165	GM19239	blood:	n/a
46	chr7:7776115-7776165	HRCEpiC	kidney:	n/a
47	chr7:7776115-7776165	GM12891	blood:	n/a
48	chr7:7776115-7776165	SK-N-SH	brain:	n/a
49	chr7:7776115-7776165	HEEpiC	esophagus:	n/a
50	chr7:7776115-7776165	HUVEC	blood vessel:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:7772333..7774684-chr7:7827758..7829772,2	MCF-7	breast:
2	chr7:7777111..7778841-chr7:7780789..7783193,3	MCF-7	breast:
3	chr7:7775020..7777800-chr7:7778182..7779689,2	K562	blood:
4	chr7:7756124..7759013-chr7:7778482..7780690,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPA3-2	chr7:7778270-7778615	ENSG00000234718.5
2	lnc-RPA3-1	chr7:7775374-7776482	NONHSAT119131

No data

Variant related genes	Relation type
ENSG00000270314	TF binding region
ENSG00000270314	CpG island
ENSG00000106399	chromatin interactions
ENSG00000269721	chromatin interactions
ENSG00000234718	chromatin interactions
ENSG00000270314	chromatin interactions

Extended variants
information (count: 201 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:201 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10952069	chr7:7774684-7774685	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10952070	chr7:7774687-7774688	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs148174018	chr7:7774704-7774705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551575756	chr7:7774712-7774713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548207371	chr7:7774780-7774781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145252378	chr7:7774797-7774798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191891728	chr7:7774833-7774834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs202046769	chr7:7774855-7774856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552173453	chr7:7774859-7774860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559875515	chr7:7774912-7774913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533489681	chr7:7774944-7774945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79597231	chr7:7774990-7774991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs17136942	chr7:7774999-7775000	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs537154776	chr7:7775026-7775027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs17136944	chr7:7775031-7775032	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs556649937	chr7:7775044-7775045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs71014707	chr7:7775045-7775046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs79018231	chr7:7775057-7775058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs74443697	chr7:7775058-7775059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374875507	chr7:7775072-7775073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368348745	chr7:7775079-7775080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548956164	chr7:7775088-7775089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567412149	chr7:7775101-7775102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184236055	chr7:7775110-7775111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs147608213	chr7:7775111-7775112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567821707	chr7:7775126-7775127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs77218571	chr7:7775164-7775165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12154244	chr7:7775165-7775166	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs575151159	chr7:7775166-7775167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113397999	chr7:7775196-7775197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561743203	chr7:7775204-7775205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113019976	chr7:7775229-7775230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541499079	chr7:7775238-7775239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559554445	chr7:7775241-7775242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533593115	chr7:7775247-7775248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143511965	chr7:7775274-7775275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554009854	chr7:7775285-7775286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113366367	chr7:7775292-7775293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531220512	chr7:7775293-7775294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113075445	chr7:7775307-7775308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567251276	chr7:7775320-7775321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187561866	chr7:7775321-7775322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190868591	chr7:7775336-7775337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12154979	chr7:7775351-7775352	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs575992050	chr7:7775412-7775413	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs77221044	chr7:7775429-7775430	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs12154665	chr7:7775435-7775436	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs146370878	chr7:7775471-7775472	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs17136953	chr7:7775515-7775516	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs138374378	chr7:7775535-7775536	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Melanoma	18172304	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
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7737600-7778800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr7:7752600-7790400	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr7:7759000-7785800	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr7:7759400-7791200	Weak transcription	Esophagus	oesophagus
5	chr7:7759600-7779000	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr7:7759600-7780000	Weak transcription	Primary T cells from cord blood	blood
7	chr7:7759600-7786800	Weak transcription	Aorta	Aorta
8	chr7:7759800-7776800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr7:7760800-7778400	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr7:7760800-7785200	Weak transcription	Primary B cells from cord blood	blood
11	chr7:7761000-7777800	Weak transcription	Thymus	Thymus
12	chr7:7767400-7776400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr7:7771000-7776400	Weak transcription	Fetal Muscle Trunk	muscle
14	chr7:7771000-7785600	Weak transcription	Pancreas	Pancrea
15	chr7:7771200-7785800	Weak transcription	Fetal Intestine Small	intestine
16	chr7:7771600-7775800	Weak transcription	Fetal Muscle Leg	muscle
17	chr7:7771600-7783000	Weak transcription	Ovary	ovary
18	chr7:7771600-7784800	Weak transcription	Stomach Smooth Muscle	stomach
19	chr7:7771600-7785400	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr7:7771600-7791000	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr7:7772000-7786000	Weak transcription	Brain Germinal Matrix	brain
22	chr7:7772200-7775800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr7:7772200-7784800	Weak transcription	Fetal Heart	heart
24	chr7:7772400-7777200	Weak transcription	Stomach Mucosa	stomach
25	chr7:7772800-7777400	Weak transcription	Rectal Smooth Muscle	rectum
26	chr7:7772800-7778600	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr7:7773000-7775800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:7773000-7776000	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr7:7773000-7777000	Weak transcription	A549	lung
30	chr7:7773000-7777400	Weak transcription	Colon Smooth Muscle	Colon
31	chr7:7773000-7778800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr7:7773000-7802000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr7:7773200-7775800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr7:7773200-7776000	Weak transcription	HSMMtube	muscle
35	chr7:7773200-7777400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr7:7773200-7778200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr7:7773200-7778200	Weak transcription	Brain Substantia Nigra	brain
38	chr7:7773400-7777200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr7:7773800-7778200	Weak transcription	HSMM	muscle
40	chr7:7773800-7778400	Weak transcription	HepG2	liver
41	chr7:7774400-7779000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr7:7774600-7775600	Weak transcription	Dnd41	blood
43	chr7:7775400-7778200	Weak transcription	GM12878-XiMat	blood
44	chr7:7775600-7776600	Enhancers	Dnd41	blood
45	chr7:7775800-7776000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr7:7775800-7777000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr7:7775800-7777000	Enhancers	Fetal Muscle Leg	muscle
48	chr7:7775800-7777200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr7:7775800-7777600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:7776000-7776200	Enhancers	HSMMtube	muscle

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