Variant report

Variant	esv1806279
Chromosome Location	chr20:23956609-23980100
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	ARID3A	chr20:23976814-23977193	HepG2	liver:	n/a	n/a
2	BATF	chr20:23965266-23965679	GM12878	blood:	n/a	n/a
3	BCL11A	chr20:23959204-23959390	GM12878	blood:	n/a	chr20:23959323-23959332
4	BCL11A	chr20:23965025-23965194	GM12878	blood:	n/a	n/a
5	BCL11A	chr20:23957003-23957211	GM12878	blood:	n/a	n/a
6	BCL11A	chr20:23965421-23965603	GM12878	blood:	n/a	n/a
7	BCL11A	chr20:23970694-23970943	GM12878	blood:	n/a	n/a
8	BCL11A	chr20:23959584-23959850	GM12878	blood:	n/a	n/a
9	BCL3	chr20:23960441-23961293	GM12878	blood:	n/a	chr20:23960654-23960662
10	BCL3	chr20:23960521-23961246	GM12878	blood:	n/a	chr20:23960654-23960662
11	BHLHE40	chr20:23976881-23977143	GM12878	blood:	n/a	n/a
12	CEBPB	chr20:23961806-23961982	HepG2	liver:	n/a	n/a
13	CEBPB	chr20:23961774-23962025	HepG2	liver:	n/a	n/a
14	CTCF	chr20:23976900-23977050	HPAF	blood vessel:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
15	CTCF	chr20:23974118-23974138	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr20:23976856-23977144	Medullo	brain:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
17	CTCF	chr20:23979143-23979240	HepG2	liver:	n/a	n/a
18	CTCF	chr20:23965160-23965310	AoAF	blood vessel:	n/a	chr20:23965234-23965243
19	CTCF	chr20:23977200-23977350	HMEC	breast:	n/a	n/a
20	CTCF	chr20:23965280-23965430	GM12878	blood:	n/a	n/a
21	CTCF	chr20:23977225-23977341	GM10266	blood:	n/a	n/a
22	CTCF	chr20:23976940-23977090	MCF-7	breast:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
23	CTCF	chr20:23959280-23959430	GM12878	blood:	n/a	chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959384-23959402 chr20:23959386-23959407
24	CTCF	chr20:23959280-23959430	HEK293	kidney:	n/a	chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959384-23959402 chr20:23959386-23959407
25	CTCF	chr20:23959201-23959479	K562	blood:	n/a	chr20:23959276-23959289 chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959384-23959402 chr20:23959386-23959407
26	CTCF	chr20:23976940-23977090	SK-N-SH_RA	brain:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
27	CTCF	chr20:23965180-23965330	GM12872	blood:	n/a	chr20:23965234-23965243
28	CTCF	chr20:23965200-23965350	GM12865	blood:	n/a	chr20:23965234-23965243
29	CTCF	chr20:23976940-23977090	GM12875	blood:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
30	CTCF	chr20:23965180-23965330	GM12865	blood:	n/a	chr20:23965234-23965243
31	CTCF	chr20:23965296-23965543	H1-hESC	embryonic stem cell:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965413-23965434
32	CTCF	chr20:23976878-23977093	K562	blood:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
33	CTCF	chr20:23965200-23965350	GM12870	blood:	n/a	chr20:23965234-23965243
34	CTCF	chr20:23965287-23965569	GM13977	blood:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965413-23965434
35	CTCF	chr20:23965117-23965747	K562	blood:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965234-23965243 chr20:23965413-23965434
36	CTCF	chr20:23965340-23965490	Hela-S3	cervix:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965413-23965434
37	CTCF	chr20:23965038-23965721	A549	lung:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965234-23965243 chr20:23965413-23965434
38	CTCF	chr20:23976880-23977030	GM12878	blood:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
39	CTCF	chr20:23976768-23977270	HCT-116	colon:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
40	CTCF	chr20:23959328-23959490	GM12892	blood:	n/a	chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959384-23959402 chr20:23959386-23959407
41	CTCF	chr20:23965440-23965590	HepG2	liver:	n/a	n/a
42	CTCF	chr20:23976900-23977050	AoAF	blood vessel:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
43	CTCF	chr20:23976900-23977050	AG09309	skin:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
44	CTCF	chr20:23976940-23977090	HMEC	breast:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
45	CTCF	chr20:23976900-23977050	NB4	blood:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
46	CTCF	chr20:23976940-23977090	NHEK	skin:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
47	CTCF	chr20:23976860-23977010	MCF-7	breast:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
48	CTCF	chr20:23977280-23977430	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr20:23965235-23965560	K562	blood:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965413-23965434
50	CTCF	chr20:23965260-23965410	GM12801	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23972451-23972501	PANC-1	pancreas:	n/a
2	chr20:23969429-23969479	AG09309	skin:	n/a
3	chr20:23972451-23972501	HL-60	blood:	n/a
4	chr20:23969397-23969447	HMEC	breast:	n/a
5	chr20:23972451-23972501	U87	brain:	n/a
6	chr20:23965921-23965971	PFSK-1	brain:	n/a
7	chr20:23965921-23965971	NH-A	brain:	n/a
8	chr20:23969397-23969447	SAEC	small airway:	n/a
9	chr20:23969429-23969479	HAEpiC	amniotic membrane:	n/a
10	chr20:23965921-23965971	AG04449	skin:	fetal
11	chr20:23969832-23969882	MCF10A-Er-Src	breast:	n/a
12	chr20:23969429-23969479	HRPEpiC	eye:	n/a
13	chr20:23965841-23965891	GM06990	blood:	n/a
14	chr20:23969237-23969287	Hela-S3	cervix:	n/a
15	chr20:23969237-23969287	HepG2	liver:	n/a
16	chr20:23969832-23969882	BJ	skin:	n/a
17	chr20:23968830-23968880	T-47D	breast:	n/a
18	chr20:23968830-23968880	HIPEpiC	eye:	n/a
19	chr20:23972451-23972501	MCF10A-Er-Src	breast:	n/a
20	chr20:23970162-23970212	HCF	heart:	n/a
21	chr20:23972451-23972501	NHBE	bronchial:	n/a
22	chr20:23970162-23970212	BJ	skin:	n/a
23	chr20:23965921-23965971	HCM	heart:	n/a
24	chr20:23969397-23969447	ECC-1	luminal epithelium:	n/a
25	chr20:23968830-23968880	CMK	blood:	n/a
26	chr20:23970162-23970212	PANC-1	pancreas:	n/a
27	chr20:23965921-23965971	IMR90	lung:	fetal
28	chr20:23972451-23972501	GM12891	blood:	n/a
29	chr20:23969397-23969447	HIPEpiC	eye:	n/a
30	chr20:23969237-23969287	BE2_C	brain:	n/a
31	chr20:23969397-23969447	GM12878	blood:	n/a
32	chr20:23965841-23965891	CMK	blood:	n/a
33	chr20:23969397-23969447	SKMC	muscle:	n/a
34	chr20:23970162-23970212	NT2-D1	testis:	n/a
35	chr20:23969397-23969447	HUVEC	blood vessel:	n/a
36	chr20:23970162-23970212	AG09319	gingival:	n/a
37	chr20:23969832-23969882	ProgFib	skin:	n/a
38	chr20:23969397-23969447	MCF10A-Er-Src	breast:	n/a
39	chr20:23965841-23965891	GM12892	blood:	n/a
40	chr20:23969429-23969479	NHDF-neo	bronchial:	n/a
41	chr20:23965921-23965971	HIPEpiC	eye:	n/a
42	chr20:23969429-23969479	HPAEpiC	pulmonary alveolar:	n/a
43	chr20:23969237-23969287	HL-60	blood:	n/a
44	chr20:23969237-23969287	SK-N-MC	brain:	n/a
45	chr20:23969237-23969287	GM12878	blood:	n/a
46	chr20:23968830-23968880	SKMC	muscle:	n/a
47	chr20:23972451-23972501	Caco-2	colon:	n/a
48	chr20:23969432-23969482	GM06990	blood:	n/a
49	chr20:23968830-23968880	HMEC	breast:	n/a
50	chr20:23969237-23969287	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr20:23976507..23978682-chr20:23981230..23983499,2	K562	blood:
2	chr20:23918328..23919972-chr20:23977586..23980315,2	MCF-7	breast:
3	chr20:23870329..23871235-chr20:23976503..23977926,6	MCF-7	breast:
4	chr20:23979873..23982563-chr20:23986456..23988446,2	MCF-7	breast:
5	chr20:23870254..23870831-chr20:23976722..23977413,2	MCF-7	breast:
6	chr20:23917806..23918382-chr20:23976746..23977457,2	MCF-7	breast:
7	chr20:23917673..23918874-chr20:23976593..23977514,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GGTLC1-1	chr20:23979070-23979425	XLOC_013696

Variant related genes	Relation type
GGTLC1	TF binding region
ENSG00000236168	TF binding region
POM121L3P	TF binding region
GGTLC1	CpG island
ENSG00000236168	CpG island
POM121L3P	CpG island
BACH2	miRNA target sites

Extended variants
information (count: 882 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:882 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143954987	chr20:23956609-23956610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs6114395	chr20:23956612-23956613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs578070917	chr20:23956639-23956640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545334269	chr20:23956717-23956718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs530491842	chr20:23956724-23956725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148208929	chr20:23956759-23956760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs141198072	chr20:23956766-23956767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529749123	chr20:23956794-23956795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185029141	chr20:23956821-23956822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188551956	chr20:23956846-23956847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538851739	chr20:23956870-23956871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79600526	chr20:23956881-23956882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560826794	chr20:23956882-23956883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150783146	chr20:23956883-23956884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537009679	chr20:23956924-23956925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556941753	chr20:23956926-23956927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs73902516	chr20:23956954-23956955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536341526	chr20:23956970-23956971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139639427	chr20:23956974-23956975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573335344	chr20:23956975-23956976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2379307	chr20:23957000-23957001	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs76190680	chr20:23957004-23957005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371970146	chr20:23957012-23957013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145314482	chr20:23957044-23957045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560858569	chr20:23957077-23957078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529727590	chr20:23957124-23957125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376912761	chr20:23957142-23957143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1555472	chr20:23957181-23957182	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs77217870	chr20:23957223-23957224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79924440	chr20:23957224-23957225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560212258	chr20:23957228-23957229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561165602	chr20:23957238-23957239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs180959341	chr20:23957254-23957255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111934170	chr20:23957286-23957287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183595430	chr20:23957298-23957299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147209827	chr20:23957391-23957392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2984255	chr20:23957396-23957397	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs536679611	chr20:23957408-23957409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576847220	chr20:23957420-23957421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553164573	chr20:23957434-23957435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566973317	chr20:23957462-23957463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539188519	chr20:23957533-23957534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189492910	chr20:23957536-23957537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575949320	chr20:23957537-23957538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182551201	chr20:23957561-23957562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555268927	chr20:23957582-23957583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149759207	chr20:23957591-23957592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4011419	chr20:23957604-23957605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113826109	chr20:23957607-23957608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145704759	chr20:23957661-23957662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
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
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23948800-23959000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:23955800-23956800	Enhancers	Dnd41	blood
3	chr20:23956200-23959000	Weak transcription	Fetal Muscle Trunk	muscle
4	chr20:23956800-23958600	Weak transcription	Dnd41	blood
5	chr20:23958600-23959000	Enhancers	Dnd41	blood
6	chr20:23959000-23959200	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr20:23959000-23959200	Enhancers	Fetal Thymus	thymus
8	chr20:23959000-23959200	Enhancers	Lung	lung
9	chr20:23959000-23959200	Flanking Active TSS	Dnd41	blood
10	chr20:23959000-23959400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr20:23959000-23959400	Enhancers	Primary T cells fromperipheralblood	blood
12	chr20:23959000-23959600	Enhancers	Fetal Stomach	stomach
13	chr20:23959000-23963400	Enhancers	Fetal Muscle Trunk	muscle
14	chr20:23959200-23959400	Enhancers	Dnd41	blood
15	chr20:23959200-23959600	Enhancers	A549	lung
16	chr20:23959200-23960400	Enhancers	Primary B cells from cord blood	blood
17	chr20:23959200-23960800	Enhancers	Primary B cells from peripheral blood	blood
18	chr20:23959400-23959600	Flanking Active TSS	Dnd41	blood
19	chr20:23959400-23960000	Weak transcription	Lung	lung
20	chr20:23959400-23960600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr20:23959400-23962200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr20:23959600-23960000	Weak transcription	Fetal Stomach	stomach
23	chr20:23959600-23960000	Weak transcription	A549	lung
24	chr20:23959600-23961000	Enhancers	Dnd41	blood
25	chr20:23960000-23960200	Enhancers	A549	lung
26	chr20:23960000-23960400	ZNF genes & repeats	Fetal Stomach	stomach
27	chr20:23960000-23960800	Enhancers	Pancreas	Pancrea
28	chr20:23960000-23961400	Active TSS	Lung	lung
29	chr20:23960200-23963200	Weak transcription	A549	lung
30	chr20:23960200-23963400	Enhancers	Fetal Muscle Leg	muscle
31	chr20:23960400-23960600	Enhancers	Fetal Kidney	kidney
32	chr20:23960400-23960600	Enhancers	Fetal Lung	lung
33	chr20:23960400-23960800	Enhancers	Esophagus	oesophagus
34	chr20:23960400-23960800	Weak transcription	Fetal Thymus	thymus
35	chr20:23960400-23963400	Enhancers	Fetal Stomach	stomach
36	chr20:23960600-23960800	Flanking Active TSS	Duodenum Mucosa	Duodenum
37	chr20:23960600-23961200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr20:23960600-23961200	Flanking Active TSS	Fetal Kidney	kidney
39	chr20:23960600-23961200	Flanking Active TSS	Fetal Lung	lung
40	chr20:23960600-23961400	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr20:23960600-23961800	Enhancers	Fetal Heart	heart
42	chr20:23960600-23962400	Enhancers	HepG2	liver
43	chr20:23960800-23961200	ZNF genes & repeats	Esophagus	oesophagus
44	chr20:23960800-23961400	Genic enhancers	Pancreas	Pancrea
45	chr20:23960800-23962000	Enhancers	Right Ventricle	heart
46	chr20:23961000-23961200	Flanking Active TSS	Fetal Brain Male	brain
47	chr20:23961000-23961400	Enhancers	Right Atrium	heart
48	chr20:23961000-23961800	Enhancers	Fetal Thymus	thymus
49	chr20:23961000-23962800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr20:23961000-23963000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland

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