Variant report

Variant	nsv2880
Chromosome Location	chr2:113716802-113736921
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:292)
CpG islands
(count:427)
Chromatin interactive
region (count:14)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:113724613-113724801	K562	blood:	n/a	n/a
2	BCL3	chr2:113735104-113735453	GM12878	blood:	n/a	chr2:113735299-113735308
3	BHLHE40	chr2:113716417-113717084	K562	blood:	n/a	n/a
4	CBX3	chr2:113716371-113717044	K562	blood:	n/a	n/a
5	CEBPB	chr2:113720388-113720637	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr2:113716320-113716969	K562	blood:	n/a	chr2:113716792-113716803 chr2:113716531-113716542 chr2:113716792-113716803
7	CEBPB	chr2:113720379-113720688	K562	blood:	n/a	n/a
8	CHD2	chr2:113718386-113718417	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr2:113716940-113717090	NHEK	skin:	n/a	chr2:113716952-113716970
10	CTCF	chr2:113717208-113717257	GM12891	blood:	n/a	n/a
11	CTCF	chr2:113717940-113718090	HRE	kidney:	n/a	chr2:113718007-113718020
12	CTCF	chr2:113716383-113717145	K562	blood:	n/a	chr2:113716952-113716970
13	CTCF	chr2:113716820-113716970	AG04449	skin:	n/a	chr2:113716952-113716970
14	CTCF	chr2:113717920-113718070	A549	lung:	n/a	chr2:113718007-113718020
15	CTCF	chr2:113717860-113718010	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr2:113716880-113717030	GM12873	blood:	n/a	chr2:113716952-113716970
17	CTCF	chr2:113716900-113717050	AoAF	blood vessel:	n/a	chr2:113716952-113716970
18	CTCF	chr2:113717938-113718072	Hela-S3	cervix:	n/a	chr2:113718007-113718020
19	CTCF	chr2:113716898-113717005	GM13976	blood:	n/a	chr2:113716952-113716970
20	CTCF	chr2:113717910-113718119	MCF-7	breast:	n/a	chr2:113718007-113718020
21	CTCF	chr2:113716914-113717014	ProgFib	skin:	n/a	chr2:113716952-113716970
22	CTCF	chr2:113718040-113718190	HFF-Myc	foreskin:	n/a	chr2:113718176-113718189
23	CTCF	chr2:113716896-113717017	GM10266	blood:	n/a	chr2:113716952-113716970
24	CTCF	chr2:113718000-113718150	A549	lung:	n/a	chr2:113718007-113718020
25	CTCF	chr2:113718036-113718041	ProgFib	skin:	n/a	n/a
26	CTCF	chr2:113717480-113717630	GM12866	blood:	n/a	n/a
27	CTCF	chr2:113716831-113717062	HepG2	liver:	n/a	chr2:113716952-113716970
28	CTCF	chr2:113716860-113717010	HEK293	kidney:	n/a	chr2:113716952-113716970
29	CTCF	chr2:113717060-113717210	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr2:113716820-113716970	GM12867	blood:	n/a	chr2:113716952-113716970
31	CTCF	chr2:113717900-113718050	SAEC	small airway:	n/a	chr2:113718007-113718020
32	CTCF	chr2:113718060-113718210	BE2_C	brain:	n/a	chr2:113718176-113718189
33	CTCF	chr2:113730500-113730650	HMEC	breast:	n/a	chr2:113730634-113730643
34	CTCF	chr2:113717980-113718130	SAEC	small airway:	n/a	chr2:113718007-113718020
35	CTCF	chr2:113716853-113717015	Pancreas_OC	pancreas:	n/a	chr2:113716952-113716970
36	CTCF	chr2:113716740-113716890	GM12801	blood:	n/a	n/a
37	CTCF	chr2:113717880-113718030	HA-sp	spinal cord:	n/a	chr2:113718007-113718020
38	CTCF	chr2:113717120-113717270	HEK293	kidney:	n/a	n/a
39	CTCF	chr2:113718013-113718080	MCF-7	breast:	n/a	n/a
40	CTCF	chr2:113717876-113718110	K562	blood:	n/a	chr2:113718007-113718020
41	CTCF	chr2:113717940-113718090	AG09319	gingival:	n/a	chr2:113718007-113718020
42	CTCF	chr2:113716840-113716990	AG04450	lung:	n/a	chr2:113716952-113716970
43	CTCF	chr2:113716873-113717007	GM12892	blood:	n/a	chr2:113716952-113716970
44	CTCF	chr2:113717080-113717230	GM12866	blood:	n/a	n/a
45	CTCF	chr2:113716860-113717010	HMEC	breast:	n/a	chr2:113716952-113716970
46	CTCF	chr2:113716857-113717043	MCF-7	breast:	n/a	chr2:113716952-113716970
47	CTCF	chr2:113716364-113717210	MCF-7	breast:	n/a	chr2:113716952-113716970
48	CTCF	chr2:113716820-113716970	HEEpiC	esophagus:	n/a	chr2:113716952-113716970
49	CTCF	chr2:113717940-113718090	HCPEpiC	choroid plexus:	n/a	chr2:113718007-113718020
50	CTCF	chr2:113717964-113718003	IMR90	lung:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:113735503-113735553	PANC-1	pancreas:	n/a
2	chr2:113735612-113735662	MCF-7	breast:	n/a
3	chr2:113735451-113735501	NB4	blood:	n/a
4	chr2:113734107-113734157	IMR90	lung:	fetal
5	chr2:113735612-113735662	SAEC	small airway:	n/a
6	chr2:113735612-113735662	AG09319	gingival:	n/a
7	chr2:113735377-113735427	PrEC	prostate:	n/a
8	chr2:113735503-113735553	HCPEpiC	choroid plexus:	n/a
9	chr2:113735377-113735427	HRE	kidney:	n/a
10	chr2:113735503-113735553	PFSK-1	brain:	n/a
11	chr2:113735377-113735427	BJ	skin:	n/a
12	chr2:113735612-113735662	H1-hESC	embryonic stem cell:	embryo
13	chr2:113736044-113736094	NB4	blood:	n/a
14	chr2:113736044-113736094	SK-N-SH	brain:	n/a
15	chr2:113735612-113735662	GM06990	blood:	n/a
16	chr2:113735503-113735553	HepG2	liver:	n/a
17	chr2:113735377-113735427	RPTEC	kidney:	n/a
18	chr2:113735377-113735427	SK-N-MC	brain:	n/a
19	chr2:113736044-113736094	HEEpiC	esophagus:	n/a
20	chr2:113735377-113735427	NT2-D1	testis:	n/a
21	chr2:113736044-113736094	Hela-S3	cervix:	n/a
22	chr2:113734107-113734157	HEEpiC	esophagus:	n/a
23	chr2:113734107-113734157	Jurkat	blood:	n/a
24	chr2:113734107-113734157	NT2-D1	testis:	n/a
25	chr2:113735503-113735553	A549	lung:	n/a
26	chr2:113735451-113735501	HCT-116	colon:	n/a
27	chr2:113735451-113735501	HIPEpiC	eye:	n/a
28	chr2:113735451-113735501	CMK	blood:	n/a
29	chr2:113735503-113735553	MCF10A-Er-Src	breast:	n/a
30	chr2:113735404-113735454	IMR90	lung:	fetal
31	chr2:113736044-113736094	GM06990	blood:	n/a
32	chr2:113735612-113735662	AG04450	lung:	fetal
33	chr2:113736044-113736094	HRCEpiC	kidney:	n/a
34	chr2:113735612-113735662	SK-N-MC	brain:	n/a
35	chr2:113736044-113736094	GM19239	blood:	n/a
36	chr2:113735404-113735454	U87	brain:	n/a
37	chr2:113735377-113735427	AG04449	skin:	fetal
38	chr2:113735404-113735454	K562	blood:	n/a
39	chr2:113735451-113735501	HNPCEpiC	eye:	n/a
40	chr2:113735503-113735553	U87	brain:	n/a
41	chr2:113735451-113735501	K562	blood:	n/a
42	chr2:113734107-113734157	HPAEpiC	pulmonary alveolar:	n/a
43	chr2:113735451-113735501	HepG2	liver:	n/a
44	chr2:113735451-113735501	PrEC	prostate:	n/a
45	chr2:113735612-113735662	AG09309	skin:	n/a
46	chr2:113734107-113734157	U87	brain:	n/a
47	chr2:113735404-113735454	HMEC	breast:	n/a
48	chr2:113735503-113735553	AG04450	lung:	fetal
49	chr2:113735612-113735662	ProgFib	skin:	n/a
50	chr2:113736044-113736094	HAEpiC	amniotic membrane:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:113716265..113720193-chr2:113720770..113723429,3	MCF-7	breast:
2	chr2:113719430..113721104-chr2:113727150..113729244,2	K562	blood:
3	chr2:113731136..113733216-chr2:113735031..113736670,2	K562	blood:
4	chr2:113729798..113732687-chr2:113732770..113734292,2	MCF-7	breast:
5	chr2:113733169..113734691-chr2:113735565..113737676,2	MCF-7	breast:
6	chr2:113506982..113507826-chr2:113716083..113717303,4	MCF-7	breast:
7	chr2:113504578..113507107-chr2:113715041..113717876,2	MCF-7	breast:
8	chr2:113718593..113720289-chr2:113834611..113837557,2	MCF-7	breast:
9	chr2:113506583..113509292-chr2:113716187..113718342,2	K562	blood:
10	chr2:113506786..113507995-chr2:113716136..113717026,4	K562	blood:
11	chr2:113719430..113721104-chr2:113727150..113729244,2	K562	blood:
12	chr2:113507343..113507937-chr2:113716373..113717003,2	MCF-7	breast:
13	chr2:113716265..113720193-chr2:113720770..113723429,3	MCF-7	breast:
14	chr2:113717657..113719208-chr2:113861543..113864051,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL36G-1	chr2:113724814-113724969	ucscGeneNc_uc002tjs_2
2	lnc-IL36G-1	chr2:113733311-113733631	ucscGeneNc_uc002tjs_2
3	lnc-IL36G-1	chr2:113729437-113729596	ucscGeneNc_uc002tjs_2

No data

Variant related genes	Relation type
IL36G	TF binding region
IL36G	CpG island
ENSG00000136688	chromatin interactions

Extended variants
information (count: 520 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:520 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs367641277	chr2:113716805-113716806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs571864335	chr2:113716826-113716827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530116997	chr2:113716830-113716831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371251537	chr2:113716843-113716844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs76262499	chr2:113716855-113716856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189026637	chr2:113716877-113716878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574779704	chr2:113716879-113716880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565510155	chr2:113716897-113716898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556211530	chr2:113716907-113716908	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569730117	chr2:113716916-113716917	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534818366	chr2:113716980-113716981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576711966	chr2:113717009-113717010	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs77576047	chr2:113717037-113717038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181705954	chr2:113717042-113717043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577863417	chr2:113717067-113717068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs116763389	chr2:113717108-113717109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571508939	chr2:113717114-113717115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs13415005	chr2:113717129-113717130	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs573855461	chr2:113717170-113717171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147729657	chr2:113717175-113717176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562530914	chr2:113717183-113717184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs13415097	chr2:113717185-113717186	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs140897855	chr2:113717213-113717214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565481439	chr2:113717229-113717230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142502676	chr2:113717241-113717242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs527972168	chr2:113717242-113717243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184822704	chr2:113717248-113717249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs67784503	chr2:113717249-113717250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs56126413	chr2:113717254-113717255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs386649271	chr2:113717303-113717304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375434535	chr2:113717320-113717321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369533102	chr2:113717358-113717359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561167900	chr2:113717361-113717362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559119200	chr2:113717362-113717363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs13417820	chr2:113717364-113717365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529036792	chr2:113717370-113717371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs56135174	chr2:113717371-113717372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs149807685	chr2:113717396-113717397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549871989	chr2:113717407-113717408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569766486	chr2:113717433-113717434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs367996361	chr2:113717446-113717447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538692510	chr2:113717466-113717467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs72942467	chr2:113717473-113717474	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs571482902	chr2:113717497-113717498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs13426809	chr2:113717524-113717525	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs79479313	chr2:113717525-113717526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79665416	chr2:113717539-113717540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553752518	chr2:113717563-113717564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574225083	chr2:113717589-113717590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190273716	chr2:113717595-113717596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	17699850	CNVD
Ovarian cancer	17699850	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113715800-113720600	Weak transcription	Fetal Intestine Small	intestine
2	chr2:113716200-113717000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr2:113716200-113717200	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr2:113716400-113717000	Enhancers	Hela-S3	cervix
5	chr2:113717200-113718000	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr2:113718000-113718200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr2:113726400-113727000	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr2:113726400-113727000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
9	chr2:113726400-113727200	Enhancers	Primary T cells fromperipheralblood	blood
10	chr2:113726400-113727400	Enhancers	Primary T cells from cord blood	blood
11	chr2:113726600-113727000	Enhancers	Primary hematopoietic stem cells	blood
12	chr2:113726600-113727000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr2:113726600-113727000	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr2:113726600-113727000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr2:113726600-113727200	Enhancers	Fetal Thymus	thymus
16	chr2:113726600-113727400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr2:113729200-113731600	Enhancers	HMEC	breast
18	chr2:113729400-113729600	Enhancers	NHEK	skin
19	chr2:113729400-113731400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr2:113729600-113729800	Flanking Active TSS	NHEK	skin
21	chr2:113729600-113731200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr2:113729600-113731200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr2:113729800-113730200	Enhancers	NHEK	skin
24	chr2:113730200-113730600	Flanking Active TSS	NHEK	skin
25	chr2:113730600-113731400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr2:113730600-113731400	Enhancers	NHEK	skin
27	chr2:113731200-113734800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr2:113731400-113734800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr2:113731400-113735000	Weak transcription	NHEK	skin
30	chr2:113731600-113735200	Weak transcription	HMEC	breast
31	chr2:113733800-113734400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr2:113733800-113739200	Enhancers	Primary T cells from cord blood	blood
33	chr2:113734200-113734400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr2:113734400-113734800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr2:113734800-113735000	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr2:113734800-113735400	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr2:113734800-113735400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr2:113734800-113735800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr2:113734800-113736000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr2:113734800-113736200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr2:113735000-113735200	Enhancers	Esophagus	oesophagus
42	chr2:113735000-113735200	Enhancers	NHEK	skin
43	chr2:113735000-113735800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
44	chr2:113735000-113735800	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr2:113735000-113736800	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr2:113735200-113735400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr2:113735200-113735400	Enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr2:113735200-113735600	Enhancers	GM12878-XiMat	blood
49	chr2:113735200-113735600	Flanking Active TSS	NHEK	skin
50	chr2:113735200-113735800	Enhancers	HMEC	breast

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