Variant report

Variant	nsv585466
Chromosome Location	chr20:14706616-14862972
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1154)
CpG islands
(count:0)
Chromatin interactive
region (count:43)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1154 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14859363-14860384	HepG2	liver:	n/a	n/a
2	ATF1	chr20:14706954-14707154	K562	blood:	n/a	n/a
3	ATF2	chr20:14725297-14725726	GM12878	blood:	n/a	n/a
4	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
6	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
7	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
8	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
9	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
10	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
11	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
14	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
15	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
16	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
17	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
19	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
20	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
21	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
22	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
23	BATF	chr20:14725428-14725715	GM12878	blood:	n/a	n/a
24	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
25	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
26	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
27	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
28	BATF	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
29	BATF	chr20:14725407-14725742	GM12878	blood:	n/a	n/a
30	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
31	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
32	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
33	BCL11A	chr20:14833756-14834084	GM12878	blood:	n/a	n/a
34	BCL11A	chr20:14819190-14819731	GM12878	blood:	n/a	chr20:14819415-14819424
35	BCL11A	chr20:14813340-14813684	GM12878	blood:	n/a	n/a
36	BCL11A	chr20:14841111-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
37	BCL11A	chr20:14833719-14834115	GM12878	blood:	n/a	n/a
38	BCL11A	chr20:14813268-14813779	GM12878	blood:	n/a	n/a
39	BCL11A	chr20:14811061-14811585	GM12878	blood:	n/a	chr20:14811164-14811173
40	BCL11A	chr20:14810529-14810966	GM12878	blood:	n/a	chr20:14810705-14810714
41	BCL11A	chr20:14811187-14811493	GM12878	blood:	n/a	n/a
42	BCL11A	chr20:14859536-14859807	GM12878	blood:	n/a	n/a
43	BCL11A	chr20:14810584-14810953	GM12878	blood:	n/a	chr20:14810705-14810714
44	BCL11A	chr20:14819269-14819704	GM12878	blood:	n/a	chr20:14819415-14819424
45	BCL3	chr20:14859514-14860394	A549	lung:	n/a	chr20:14860151-14860160 chr20:14860265-14860274
46	BCL3	chr20:14859331-14860569	A549	lung:	n/a	chr20:14860151-14860160 chr20:14859419-14859428 chr20:14860265-14860274
47	BCL3	chr20:14826038-14826561	A549	lung:	n/a	chr20:14826452-14826461
48	BCL3	chr20:14825912-14826568	A549	lung:	n/a	chr20:14826452-14826461
49	BCLAF1	chr20:14819282-14819800	GM12878	blood:	n/a	chr20:14819415-14819424
50	BHLHE40	chr20:14810570-14811822	GM12878	blood:	n/a	n/a

No data

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
2	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
3	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
4	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
5	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
6	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
7	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
8	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
9	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
10	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
11	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
12	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
13	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
14	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
15	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
16	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
17	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
18	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
19	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
20	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
21	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
22	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
23	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
24	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
25	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:
26	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
27	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
28	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
29	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
30	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
31	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
32	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
33	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
34	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
35	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
36	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
37	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
38	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
39	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
40	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
41	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
42	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
43	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C20orf7-3	chr20:14830550-14830649	NONHSAT078714
2	lnc-FLRT3-4	chr20:14858021-14858161	ucscGeneNc_uc002woy_1
3	lnc-FLRT3-4	chr20:14816742-14816950	ucscGeneNc_uc002woy_1
4	lnc-FLRT3-4	chr20:14812896-14813240	ucscGeneNc_uc002woy_1
5	lnc-C20orf7-3	chr20:14830550-14831152	NONHSAT078716

No data

Variant related genes	Relation type
RPS10P2	TF binding region

Extended variants
information (count: 4213 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:4213 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4813165	chr20:14706616-14706617	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs191842750	chr20:14706620-14706621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569869237	chr20:14706648-14706649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184013541	chr20:14706662-14706663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556015289	chr20:14706726-14706727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574285227	chr20:14706733-14706734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574343092	chr20:14706790-14706791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560497345	chr20:14706863-14706864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs6074780	chr20:14706879-14706880	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs6079542	chr20:14706916-14706917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs371765919	chr20:14706935-14706936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553461400	chr20:14706937-14706938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572084200	chr20:14706995-14706996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs6074781	chr20:14707003-14707004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545870812	chr20:14707005-14707006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs6074782	chr20:14707025-14707026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs6074783	chr20:14707050-14707051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560573538	chr20:14707069-14707070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148361371	chr20:14707079-14707080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs16994837	chr20:14707127-14707128	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs6042882	chr20:14707144-14707145	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs367692358	chr20:14707281-14707282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562750248	chr20:14707317-14707318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141519240	chr20:14707331-14707332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73899274	chr20:14707334-14707335	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs188304253	chr20:14707365-14707366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565699052	chr20:14707378-14707379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs115954604	chr20:14707388-14707389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142278662	chr20:14707397-14707398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551460797	chr20:14707401-14707402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569857037	chr20:14707420-14707421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537634698	chr20:14707442-14707443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs79299417	chr20:14707466-14707467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs60302342	chr20:14707504-14707505	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs6034020	chr20:14707535-14707536	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs553711509	chr20:14707559-14707560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113458126	chr20:14707571-14707572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140175436	chr20:14707590-14707591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557873277	chr20:14707697-14707698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374975932	chr20:14707801-14707802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576233411	chr20:14707818-14707819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143852039	chr20:14707857-14707858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561698679	chr20:14707862-14707863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112413729	chr20:14707924-14707925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1932949	chr20:14707975-14707976	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs559271631	chr20:14708007-14708008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1932948	chr20:14708023-14708024	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs551393699	chr20:14708031-14708032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147238055	chr20:14708035-14708036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73262865	chr20:14708042-14708043	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Glaucoma	21310917	CNVD
Alagille syndrome	22470819	CNVD
Lung cancer	16773561	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Myelofibrosis	22110671	CNVD
Kabuki syndrome	21720541	CNVD
Glioblastoma multiforme	22286061	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Neurocytoma	17123091	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164919	CNVD
Multiple sclerosis	20663923	CNVD
Schizophrenia	20663923	CNVD
brain infarct	20663923	CNVD
Breast cancer	22522925	CNVD
Breast cancer	17142309	CNVD
Cancer	20164920	CNVD
Schizophrenia	23813976	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20531469	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Williams Syndrome	20824207	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
early-passage human iPS cells	21368824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14698600-14707000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr20:14706400-14707000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr20:14707000-14707200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr20:14707200-14709600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr20:14709400-14710200	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr20:14710000-14710200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr20:14710000-14710400	Enhancers	Liver	Liver
8	chr20:14710000-14710400	Enhancers	HepG2	liver
9	chr20:14710000-14710600	Enhancers	Stomach Mucosa	stomach
10	chr20:14710200-14710400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr20:14710400-14713000	Weak transcription	Liver	Liver
12	chr20:14710600-14712000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr20:14710600-14713000	Weak transcription	Stomach Mucosa	stomach
14	chr20:14711600-14714600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr20:14712000-14713400	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr20:14712800-14713600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr20:14713000-14713400	Enhancers	Fetal Kidney	kidney
18	chr20:14713000-14713600	Enhancers	Stomach Mucosa	stomach
19	chr20:14713000-14713800	Enhancers	Liver	Liver
20	chr20:14713200-14713600	Enhancers	Hela-S3	cervix
21	chr20:14713200-14713800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr20:14719000-14719200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr20:14719200-14721000	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr20:14720600-14721800	Enhancers	Fetal Brain Male	brain
25	chr20:14721000-14721400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr20:14721000-14721400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr20:14721000-14721800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr20:14721200-14721600	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr20:14721200-14721800	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr20:14721200-14721800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr20:14721200-14721800	Enhancers	Fetal Brain Female	brain
32	chr20:14721200-14722000	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr20:14721200-14722000	Enhancers	Brain Germinal Matrix	brain
34	chr20:14721400-14721600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr20:14721600-14726800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr20:14724800-14726200	Enhancers	GM12878-XiMat	blood
37	chr20:14726000-14727600	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr20:14726200-14726600	Enhancers	Fetal Kidney	kidney
39	chr20:14726600-14727000	Active TSS	Skeletal Muscle Female	skeletal muscle
40	chr20:14726800-14727000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr20:14727000-14727600	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr20:14738200-14738600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr20:14738400-14738600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr20:14740600-14740800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr20:14742800-14743400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr20:14743000-14744000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr20:14743400-14744200	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr20:14745200-14746200	Enhancers	Stomach Mucosa	stomach
49	chr20:14746000-14746200	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr20:14750600-14756200	Weak transcription	Psoas Muscle	Psoas

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