Variant report

Variant	nsv1027937
Chromosome Location	chr8:36434982-36572189
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:36459712-36459951	K562	blood:	n/a	n/a
2	BATF	chr8:36523177-36523383	GM12878	blood:	n/a	chr8:36523276-36523287
3	CEBPB	chr8:36447073-36447285	HepG2	liver:	n/a	n/a
4	CEBPB	chr8:36559225-36559414	HepG2	liver:	n/a	chr8:36559317-36559334 chr8:36559320-36559333 chr8:36559320-36559331
5	CTCF	chr8:36504440-36504466	LNCaP	prostate:	n/a	n/a
6	CTCF	chr8:36521540-36521690	NB4	blood:	n/a	n/a
7	CTCF	chr8:36436409-36436435	Lung_OC	lung:	n/a	n/a
8	CTCF	chr8:36485579-36485763	K562	blood:	n/a	n/a
9	CTCF	chr8:36480800-36480950	GM12871	blood:	n/a	n/a
10	CTCF	chr8:36471680-36471830	GM12867	blood:	n/a	n/a
11	CTCF	chr8:36554340-36554490	HRE	kidney:	n/a	n/a
12	E2F4	chr8:36461256-36461383	MCF10A-Er-Src	breast:	n/a	n/a
13	E2F4	chr8:36517505-36517583	MCF10A-Er-Src	breast:	n/a	n/a
14	E2F4	chr8:36441190-36441374	MCF10A-Er-Src	breast:	n/a	n/a
15	E2F4	chr8:36438659-36438690	MCF10A-Er-Src	breast:	n/a	n/a
16	E2F4	chr8:36450708-36450857	MCF10A-Er-Src	breast:	n/a	n/a
17	E2F4	chr8:36533459-36533603	MCF10A-Er-Src	breast:	n/a	n/a
18	EP300	chr8:36523169-36523371	GM12878	blood:	n/a	n/a
19	EP300	chr8:36523189-36523402	GM12878	blood:	n/a	n/a
20	FOS	chr8:36549017-36549304	MCF10A-Er-Src	breast:	n/a	chr8:36549143-36549153 chr8:36549143-36549153 chr8:36549143-36549153
21	FOS	chr8:36514915-36515036	MCF10A-Er-Src	breast:	n/a	chr8:36514972-36514982 chr8:36514974-36514981 chr8:36514972-36514982 chr8:36514973-36514981 chr8:36514973-36514981 chr8:36514972-36514982 chr8:36514972-36514982
22	FOS	chr8:36561589-36561789	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr8:36561571-36561771	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr8:36504152-36504283	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr8:36514919-36515124	MCF10A-Er-Src	breast:	n/a	chr8:36514972-36514982 chr8:36514974-36514981 chr8:36514972-36514982 chr8:36514973-36514981 chr8:36514973-36514981 chr8:36515068-36515077 chr8:36514972-36514982 chr8:36514972-36514982
26	FOS	chr8:36549021-36549304	MCF10A-Er-Src	breast:	n/a	chr8:36549143-36549153 chr8:36549143-36549153 chr8:36549143-36549153
27	FOS	chr8:36549031-36549280	MCF10A-Er-Src	breast:	n/a	chr8:36549143-36549153 chr8:36549143-36549153 chr8:36549143-36549153
28	FOS	chr8:36514919-36515053	MCF10A-Er-Src	breast:	n/a	chr8:36514972-36514982 chr8:36514974-36514981 chr8:36514972-36514982 chr8:36514973-36514981 chr8:36514973-36514981 chr8:36514972-36514982 chr8:36514972-36514982
29	FOS	chr8:36461581-36461742	MCF10A-Er-Src	breast:	n/a	n/a
30	GATA3	chr8:36446198-36446388	SH-SY5Y	brain:	n/a	n/a
31	GATA3	chr8:36442439-36442556	SH-SY5Y	brain:	n/a	n/a
32	GTF2F1	chr8:36448848-36448853	K562	blood:	n/a	n/a
33	JUN	chr8:36483765-36484035	H1-hESC	embryonic stem cell:	n/a	chr8:36483951-36483960 chr8:36483950-36483960 chr8:36483949-36483961 chr8:36483951-36483958 chr8:36483950-36483959
34	JUND	chr8:36561531-36561659	HepG2	liver:	n/a	n/a
35	JUND	chr8:36447059-36447286	HepG2	liver:	n/a	n/a
36	JUND	chr8:36483715-36484046	H1-hESC	embryonic stem cell:	n/a	chr8:36483951-36483960 chr8:36483950-36483960 chr8:36483949-36483961 chr8:36483951-36483958 chr8:36483950-36483959
37	JUND	chr8:36483736-36484205	H1-hESC	embryonic stem cell:	n/a	chr8:36483951-36483960 chr8:36483950-36483960 chr8:36483949-36483961 chr8:36483951-36483958 chr8:36483950-36483959
38	JUND	chr8:36483827-36483990	H1-hESC	embryonic stem cell:	n/a	chr8:36483951-36483960 chr8:36483950-36483960 chr8:36483949-36483961 chr8:36483951-36483958 chr8:36483950-36483959
39	MAFF	chr8:36437684-36437977	HepG2	liver:	n/a	chr8:36437802-36437820
40	MAFF	chr8:36536279-36536348	K562	blood:	n/a	chr8:36536312-36536326
41	MAFF	chr8:36539739-36539964	HepG2	liver:	n/a	chr8:36539888-36539906 chr8:36539887-36539901
42	MAFF	chr8:36437794-36437900	K562	blood:	n/a	chr8:36437802-36437820
43	MAFF	chr8:36540203-36540328	HepG2	liver:	n/a	chr8:36540284-36540298
44	MAFF	chr8:36463785-36463982	HepG2	liver:	n/a	n/a
45	MAFK	chr8:36511738-36511805	HepG2	liver:	n/a	chr8:36511756-36511771 chr8:36511756-36511772 chr8:36511756-36511767
46	MAFK	chr8:36437650-36437993	HepG2	liver:	n/a	chr8:36437804-36437815 chr8:36437805-36437816 chr8:36437876-36437893 chr8:36437804-36437815 chr8:36437804-36437819 chr8:36437805-36437816 chr8:36437803-36437817 chr8:36437804-36437820
47	MAFK	chr8:36511709-36511884	HepG2	liver:	n/a	chr8:36511756-36511771 chr8:36511756-36511772 chr8:36511756-36511767
48	MAFK	chr8:36463762-36463987	HepG2	liver:	n/a	chr8:36463842-36463857
49	MAFK	chr8:36536204-36536444	HepG2	liver:	n/a	chr8:36536308-36536323 chr8:36536309-36536320 chr8:36536308-36536324 chr8:36536311-36536327 chr8:36536309-36536329
50	MAFK	chr8:36539717-36540435	HepG2	liver:	n/a	chr8:36540284-36540298 chr8:36539889-36539904 chr8:36540281-36540301 chr8:36540074-36540089 chr8:36540090-36540110 chr8:36539884-36539904 chr8:36540092-36540108 chr8:36539887-36539901 chr8:36539886-36539902 chr8:36540283-36540299

No.	Distal block	Cell Line	Cell type
1	chr8:36532784..36534570-chr8:36538161..36540032,3	K562	blood:
2	chr8:36532784..36534570-chr8:36538161..36540032,3	K562	blood:
3	chr8:36532784..36534474-chr8:36538409..36540032,2	K562	blood:
4	chr8:36532784..36534474-chr8:36538409..36540032,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-419C23.1.1-3	chr8:36559339-36559411	ENSG00000253363.1
2	lnc-RP11-419C23.1.1-7	chr8:36438698-36439109	NONHSAT126019

Variant related genes	Relation type
RPL23P10	TF binding region

Extended variants
information (count: 1862 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:1862 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376088481	chr8:36434984-36434985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs147461103	chr8:36435083-36435084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138324349	chr8:36435112-36435113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563500339	chr8:36435122-36435123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570978098	chr8:36435159-36435160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs180948736	chr8:36435240-36435241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547120424	chr8:36435312-36435313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143906068	chr8:36435361-36435362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183660602	chr8:36435362-36435363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369176058	chr8:36435368-36435369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs367929597	chr8:36435373-36435374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113067253	chr8:36435374-36435375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188221955	chr8:36435378-36435379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34219514	chr8:36435407-36435408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554809788	chr8:36435518-36435519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542551233	chr8:36435520-36435521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147283507	chr8:36435545-36435546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148663676	chr8:36435564-36435565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537207829	chr8:36435597-36435598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558769272	chr8:36435643-36435644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553494997	chr8:36435711-36435712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577138001	chr8:36435718-36435719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545513652	chr8:36435761-36435762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560420041	chr8:36435781-36435782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535222310	chr8:36435796-36435797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572363697	chr8:36435808-36435809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371692727	chr8:36435832-36435833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182011925	chr8:36435868-36435869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142169628	chr8:36435878-36435879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs546170678	chr8:36435890-36435891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs199731116	chr8:36435897-36435898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376567519	chr8:36435900-36435901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550096808	chr8:36435911-36435912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368393823	chr8:36435929-36435930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150787961	chr8:36435980-36435981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2105482	chr8:36435994-36435995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547081833	chr8:36436001-36436002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1981325	chr8:36436055-36436056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2096482	chr8:36436081-36436082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs139209050	chr8:36436138-36436139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143975331	chr8:36436151-36436152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187380268	chr8:36436171-36436172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372233540	chr8:36436204-36436205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547892196	chr8:36436223-36436224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191751730	chr8:36436276-36436277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116281682	chr8:36436287-36436288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs75612925	chr8:36436347-36436348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532257985	chr8:36436381-36436382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs373240072	chr8:36436421-36436422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553348449	chr8:36436423-36436424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:122)

Disease	PMID	Source
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Multiple myeloma	16616336	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	21806811	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	20459607	CNVD
Renal cell carcinoma	18765545	CNVD
Colorectal cancer	16912164	CNVD
Neuroticism	17667963	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	18382360	CNVD
Ductal carcinoma	18381933	CNVD
Breast cancer	21328542	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Intellectual disability	22045946	CNVD
Lung cancer	17925434	CNVD
Uveal melanoma	20484589	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	19651600	CNVD
abnormal development	18461090	CNVD
Renal cell carcinoma	21215367	CNVD
Breast cancer	16620391	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Rhabdomyosarcoma	16790082	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:36432400-36440800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr8:36437200-36437800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr8:36437200-36438000	Enhancers	Fetal Heart	heart
4	chr8:36438000-36438800	Weak transcription	Fetal Heart	heart
5	chr8:36438800-36439000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:36438800-36439000	Enhancers	Fetal Heart	heart
7	chr8:36439000-36440200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:36439000-36440800	Weak transcription	Fetal Heart	heart
9	chr8:36440000-36440800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr8:36440000-36442000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr8:36440200-36440600	Enhancers	NHEK	skin
12	chr8:36440200-36441000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr8:36440200-36441000	Enhancers	Fetal Brain Female	brain
14	chr8:36440200-36441400	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr8:36440200-36442200	Enhancers	Adipose Nuclei	Adipose
16	chr8:36440800-36441000	Enhancers	Fetal Heart	heart
17	chr8:36440800-36441200	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr8:36440800-36441200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr8:36441400-36446000	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr8:36442000-36445800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr8:36445200-36445800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr8:36445800-36446600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr8:36446000-36446800	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr8:36457000-36457600	Enhancers	Small Intestine	intestine
25	chr8:36459400-36460000	Enhancers	Fetal Heart	heart
26	chr8:36469400-36469800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr8:36469400-36470000	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr8:36477000-36477400	Enhancers	Adipose Nuclei	Adipose
29	chr8:36479600-36479800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
30	chr8:36479800-36483400	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr8:36483400-36484200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr8:36483400-36484400	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr8:36483600-36484000	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr8:36483600-36484400	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr8:36483600-36484400	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr8:36484200-36484400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr8:36484200-36484400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr8:36485400-36485800	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr8:36485600-36487000	Enhancers	Spleen	Spleen
40	chr8:36486000-36486200	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr8:36486800-36487200	Enhancers	Fetal Heart	heart
42	chr8:36494800-36495800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr8:36495800-36499200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr8:36499200-36502400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr8:36502400-36502800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr8:36502800-36503200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr8:36503200-36503400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr8:36510400-36510800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr8:36511800-36512600	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr8:36512400-36512600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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