Variant report

Variant	nsv9508
Chromosome Location	chr17:20440129-20458176
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:90)
CpG islands
(count:488)
Chromatin interactive
region (count:0)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:90 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr17:20443708-20444186	GM12878	blood:	n/a	n/a
2	BATF	chr17:20443556-20444223	GM12878	blood:	n/a	n/a
3	BATF	chr17:20449270-20449503	GM12878	blood:	n/a	n/a
4	BCL11A	chr17:20443777-20444111	GM12878	blood:	n/a	n/a
5	BCL11A	chr17:20443676-20444145	GM12878	blood:	n/a	n/a
6	CTCF	chr17:20445560-20445710	HRPEpiC	eye:	n/a	n/a
7	CTCF	chr17:20457903-20457938	Lung_OC	lung:	n/a	n/a
8	CTCF	chr17:20445580-20445730	AG09319	gingival:	n/a	n/a
9	CTCF	chr17:20448391-20448410	Kidney_OC	kidney:	n/a	n/a
10	CTCF	chr17:20456367-20456424	GM19240	blood:	n/a	n/a
11	CTCF	chr17:20445654-20445703	LNCaP	prostate:	n/a	n/a
12	CTCF	chr17:20445560-20445710	AG10803	skin:	n/a	n/a
13	CTCF	chr17:20445580-20445730	HMEC	breast:	n/a	n/a
14	CTCF	chr17:20445599-20445741	ProgFib	skin:	n/a	n/a
15	CTCF	chr17:20445632-20445687	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr17:20445580-20445730	Caco-2	colon:	n/a	n/a
17	CTCF	chr17:20445560-20445710	AG04449	skin:	n/a	n/a
18	CTCF	chr17:20445604-20445730	MCF-7	breast:	n/a	n/a
19	CTCF	chr17:20445600-20445750	MCF-7	breast:	n/a	n/a
20	CTCF	chr17:20445620-20445770	AG09319	gingival:	n/a	n/a
21	CTCF	chr17:20445558-20445726	T-47D	breast:	n/a	n/a
22	CTCF	chr17:20445620-20445770	AG10803	skin:	n/a	n/a
23	CTCF	chr17:20445593-20445750	NHEK	skin:	n/a	n/a
24	CTCF	chr17:20445580-20445730	AG09309	skin:	n/a	n/a
25	CTCF	chr17:20452453-20452487	LNCaP	prostate:	n/a	n/a
26	CTCF	chr17:20445637-20445731	Fibrobl	skin:	n/a	n/a
27	CTCF	chr17:20445580-20445730	SAEC	small airway:	n/a	n/a
28	CTCF	chr17:20445580-20445730	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr17:20445558-20445742	Pancreas_OC	pancreas:	n/a	n/a
30	CTCF	chr17:20445642-20445704	GM10266	blood:	n/a	n/a
31	CTCF	chr17:20440911-20440950	Pancreas_OC	pancreas:	n/a	n/a
32	CTCF	chr17:20445610-20445723	MCF-7	breast:	n/a	n/a
33	CTCF	chr17:20445589-20445738	LNCaP	prostate:	n/a	n/a
34	CTCF	chr17:20445622-20445689	GM12878	blood:	n/a	n/a
35	CTCF	chr17:20445520-20445670	HMEC	breast:	n/a	n/a
36	EBF1	chr17:20443599-20444220	GM12878	blood:	n/a	chr17:20444093-20444102 chr17:20444093-20444103
37	EBF1	chr17:20443620-20444226	GM12878	blood:	n/a	chr17:20444093-20444102 chr17:20444093-20444103
38	EP300	chr17:20444145-20444524	T-47D	breast:	n/a	n/a
39	EP300	chr17:20443863-20444125	GM12878	blood:	n/a	n/a
40	FOSL2	chr17:20448386-20448629	HepG2	liver:	n/a	n/a
41	FOSL2	chr17:20453744-20454093	HepG2	liver:	n/a	n/a
42	FOSL2	chr17:20452869-20453245	HepG2	liver:	n/a	n/a
43	FOXA1	chr17:20444181-20444516	T-47D	breast:	n/a	n/a
44	FOXA1	chr17:20445123-20445312	T-47D	breast:	n/a	n/a
45	FOXA1	chr17:20444156-20444512	T-47D	breast:	n/a	n/a
46	FOXA1	chr17:20445087-20445435	T-47D	breast:	n/a	n/a
47	FOXM1	chr17:20443589-20444290	GM12878	blood:	n/a	n/a
48	FOXM1	chr17:20443701-20444186	GM12878	blood:	n/a	n/a
49	FOXP2	chr17:20444251-20444474	SK-N-MC	brain:	n/a	n/a
50	GABPA	chr17:20450160-20450376	Hela-S3	cervix:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:20456901-20456951	NHBE	bronchial:	n/a
2	chr17:20450466-20450516	PrEC	prostate:	n/a
3	chr17:20450466-20450516	RPTEC	kidney:	n/a
4	chr17:20456385-20456435	Hepatocyte	liver:	n/a
5	chr17:20456901-20456951	SK-N-SH_RA	brain:	n/a
6	chr17:20454132-20454182	A549	lung:	n/a
7	chr17:20450484-20450534	ProgFib	skin:	n/a
8	chr17:20448558-20448608	HEK293	kidney:	embryo
9	chr17:20446526-20446576	AG09319	gingival:	n/a
10	chr17:20450466-20450516	LNCaP	prostate:	n/a
11	chr17:20450484-20450534	Jurkat	blood:	n/a
12	chr17:20446526-20446576	Hela-S3	cervix:	n/a
13	chr17:20456385-20456435	ovcar-3	ovarian:	n/a
14	chr17:20448558-20448608	Caco-2	colon:	n/a
15	chr17:20456385-20456435	HCF	heart:	n/a
16	chr17:20445757-20445807	AG09319	gingival:	n/a
17	chr17:20446526-20446576	AoSMC	blood vessel:	n/a
18	chr17:20456901-20456951	A549	lung:	n/a
19	chr17:20446526-20446576	GM12891	blood:	n/a
20	chr17:20454132-20454182	GM12892	blood:	n/a
21	chr17:20456385-20456435	SAEC	small airway:	n/a
22	chr17:20450466-20450516	IMR90	lung:	fetal
23	chr17:20448558-20448608	HRCEpiC	kidney:	n/a
24	chr17:20450466-20450516	HIPEpiC	eye:	n/a
25	chr17:20456385-20456435	AG10803	skin:	n/a
26	chr17:20456901-20456951	BJ	skin:	n/a
27	chr17:20450484-20450534	HEK293	kidney:	embryo
28	chr17:20448558-20448608	SK-N-SH_RA	brain:	n/a
29	chr17:20446526-20446576	GM06990	blood:	n/a
30	chr17:20448558-20448608	HepG2	liver:	n/a
31	chr17:20450484-20450534	H1-hESC	embryonic stem cell:	embryo
32	chr17:20456901-20456951	HCPEpiC	choroid plexus:	n/a
33	chr17:20450466-20450516	Hepatocyte	liver:	n/a
34	chr17:20454132-20454182	HPAEpiC	pulmonary alveolar:	n/a
35	chr17:20450466-20450516	GM12878	blood:	n/a
36	chr17:20456385-20456435	AG09319	gingival:	n/a
37	chr17:20456385-20456435	HEK293	kidney:	embryo
38	chr17:20446526-20446576	HUVEC	blood vessel:	n/a
39	chr17:20448558-20448608	AG09319	gingival:	n/a
40	chr17:20450484-20450534	HRE	kidney:	n/a
41	chr17:20450466-20450516	NHBE	bronchial:	n/a
42	chr17:20456385-20456435	HepG2	liver:	n/a
43	chr17:20456901-20456951	NH-A	brain:	n/a
44	chr17:20456901-20456951	SK-N-SH	brain:	n/a
45	chr17:20446526-20446576	A549	lung:	n/a
46	chr17:20450466-20450516	Caco-2	colon:	n/a
47	chr17:20450484-20450534	NHDF-neo	bronchial:	n/a
48	chr17:20445757-20445807	AoSMC	blood vessel:	n/a
49	chr17:20454132-20454182	HCT-116	colon:	n/a
50	chr17:20450466-20450516	SK-N-SH	brain:	n/a

No data

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LGALS9B-12	chr17:20446789-20446842	NONHSAT146601
2	lnc-LGALS9B-12	chr17:20447359-20447436	NONHSAT146601
3	lnc-LGALS9B-12	chr17:20446287-20446510	NONHSAT146601

No data

Variant related genes	Relation type
ENSG00000230339	TF binding region
ENSG00000265916	TF binding region
TBC1D3P3	TF binding region
ENSG00000264981	TF binding region
ENSG00000267075	TF binding region
ENSG00000230339	CpG island
ENSG00000265916	CpG island
TBC1D3P3	CpG island
ENSG00000264981	CpG island
ENSG00000267075	CpG island

Extended variants
information (count: 296 )
Associated
traits (count: 150 )

Variant overlapped rSNPs/rCNVs (count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540559190	chr17:20440132-20440133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs558674889	chr17:20440264-20440265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200864438	chr17:20440490-20440491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576828827	chr17:20440621-20440622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372457371	chr17:20440741-20440742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs377089488	chr17:20441024-20441025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs370480221	chr17:20441025-20441026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574666454	chr17:20441053-20441054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542000250	chr17:20441078-20441079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373492563	chr17:20441148-20441149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs111668724	chr17:20441159-20441160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs377585337	chr17:20441222-20441223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573900160	chr17:20441249-20441250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370874128	chr17:20441266-20441267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs77414475	chr17:20441307-20441308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200399116	chr17:20441383-20441384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565816826	chr17:20441398-20441399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369074524	chr17:20441415-20441416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532159463	chr17:20441446-20441447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550666819	chr17:20441454-20441455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568950986	chr17:20441466-20441467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536386999	chr17:20441483-20441484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1678241	chr17:20441513-20441514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1678240	chr17:20441537-20441538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs1678239	chr17:20441543-20441544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184294257	chr17:20441576-20441577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548068137	chr17:20441582-20441583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111247647	chr17:20441623-20441624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375806924	chr17:20441647-20441648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377711298	chr17:20441649-20441650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558825787	chr17:20441660-20441661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371648479	chr17:20441661-20441662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537873025	chr17:20441694-20441695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556168995	chr17:20441696-20441697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574576631	chr17:20441902-20441903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542351144	chr17:20442025-20442026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201997899	chr17:20442027-20442028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572604693	chr17:20442059-20442060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546144494	chr17:20442098-20442099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201525707	chr17:20442271-20442272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564791225	chr17:20442274-20442275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534412236	chr17:20442275-20442276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373673967	chr17:20442378-20442379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376667099	chr17:20442438-20442439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs367580788	chr17:20442446-20442447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200307142	chr17:20442459-20442460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371403478	chr17:20442493-20442494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373928508	chr17:20442536-20442537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377199095	chr17:20442569-20442570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548269006	chr17:20442658-20442659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:150)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:20437000-20445200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr17:20437200-20445200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr17:20438000-20444200	Weak transcription	Fetal Thymus	thymus
4	chr17:20439000-20444200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr17:20443200-20445800	Enhancers	Primary B cells from peripheral blood	blood
6	chr17:20444200-20444400	Enhancers	Primary hematopoietic stem cells	blood
7	chr17:20444200-20444400	Enhancers	Rectal Mucosa Donor 29	rectum
8	chr17:20444200-20445400	Enhancers	Fetal Thymus	thymus
9	chr17:20444200-20445600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr17:20444200-20445800	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr17:20444200-20445800	Enhancers	GM12878-XiMat	blood
12	chr17:20444400-20445200	Weak transcription	Primary hematopoietic stem cells	blood
13	chr17:20444400-20445200	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr17:20445200-20445600	Enhancers	Primary hematopoietic stem cells	blood
15	chr17:20445200-20445600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr17:20445200-20445600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr17:20445200-20445600	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr17:20445200-20445600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr17:20445200-20445600	Enhancers	Rectal Mucosa Donor 29	rectum
20	chr17:20445200-20445800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr17:20445400-20445800	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr17:20445400-20445800	Enhancers	NHDF-Ad	bronchial
23	chr17:20457400-20457600	Enhancers	Fetal Muscle Trunk	muscle

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