Variant report

Variant	nsv1005269
Chromosome Location	chr2:34703116-34898472
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:522)
CpG islands
(count:246)
Chromatin interactive
region (count:11)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:522 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:34814574-34814687	K562	blood:	n/a	n/a
2	BATF	chr2:34881803-34882061	GM12878	blood:	n/a	n/a
3	BCL3	chr2:34803709-34804015	GM12878	blood:	n/a	n/a
4	BHLHE40	chr2:34795688-34795858	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:34891473-34891834	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:34827333-34827668	GM12878	blood:	n/a	n/a
7	CBX3	chr2:34744823-34745018	K562	blood:	n/a	n/a
8	CEBPB	chr2:34876038-34876081	K562	blood:	n/a	n/a
9	CEBPB	chr2:34706631-34706981	IMR90	lung:	n/a	chr2:34706794-34706805
10	CEBPB	chr2:34736004-34736033	HepG2	liver:	n/a	chr2:34736017-34736028
11	CEBPB	chr2:34706676-34706941	A549	lung:	n/a	chr2:34706794-34706805
12	CEBPB	chr2:34759886-34760188	MCF-7	breast:	n/a	chr2:34759972-34759985
13	CEBPB	chr2:34850841-34851040	A549	lung:	n/a	chr2:34850939-34850950 chr2:34850903-34850914
14	CEBPB	chr2:34717914-34718139	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:34788007-34788119	K562	blood:	n/a	chr2:34788088-34788101 chr2:34788090-34788101 chr2:34788088-34788101 chr2:34788090-34788101
16	CEBPB	chr2:34795632-34795901	MCF-7	breast:	n/a	n/a
17	CEBPB	chr2:34840044-34840132	A549	lung:	n/a	n/a
18	CEBPB	chr2:34706655-34707006	MCF-7	breast:	n/a	chr2:34706794-34706805
19	CEBPB	chr2:34759749-34759988	HepG2	liver:	n/a	chr2:34759832-34759845 chr2:34759832-34759843 chr2:34759972-34759985
20	CEBPB	chr2:34759877-34760165	K562	blood:	n/a	chr2:34759972-34759985
21	CEBPB	chr2:34803766-34804113	MCF-7	breast:	n/a	n/a
22	CEBPB	chr2:34706608-34706989	HepG2	liver:	n/a	chr2:34706794-34706805
23	CEBPB	chr2:34706625-34706972	K562	blood:	n/a	chr2:34706794-34706805
24	CEBPB	chr2:34717910-34718155	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr2:34793002-34793270	HepG2	liver:	n/a	chr2:34793159-34793170 chr2:34793159-34793172 chr2:34793160-34793171
26	CEBPB	chr2:34706730-34706928	H1-hESC	embryonic stem cell:	n/a	chr2:34706794-34706805
27	CEBPB	chr2:34759033-34759047	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:34850814-34851079	HepG2	liver:	n/a	chr2:34850939-34850950 chr2:34850903-34850914
29	CHD1	chr2:34795620-34795779	GM12878	blood:	n/a	n/a
30	CHD2	chr2:34881819-34881970	GM12878	blood:	n/a	n/a
31	CHD2	chr2:34826745-34826921	GM12878	blood:	n/a	n/a
32	CHD2	chr2:34827312-34827671	GM12878	blood:	n/a	n/a
33	CTCF	chr2:34795637-34795862	GM19238	blood:	n/a	n/a
34	CTCF	chr2:34795660-34795810	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr2:34795651-34795865	K562	blood:	n/a	n/a
36	CTCF	chr2:34795640-34795790	HAc	cerebellar:	n/a	n/a
37	CTCF	chr2:34795620-34795770	GM12868	blood:	n/a	n/a
38	CTCF	chr2:34795373-34796072	MCF-7	breast:	n/a	n/a
39	CTCF	chr2:34795680-34795830	SAEC	small airway:	n/a	n/a
40	CTCF	chr2:34795720-34795870	GM12871	blood:	n/a	n/a
41	CTCF	chr2:34772320-34772470	NHEK	skin:	n/a	n/a
42	CTCF	chr2:34795680-34795830	GM12871	blood:	n/a	n/a
43	CTCF	chr2:34795541-34795937	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr2:34772480-34772630	GM12867	blood:	n/a	n/a
45	CTCF	chr2:34772820-34772970	GM12874	blood:	n/a	n/a
46	CTCF	chr2:34795630-34795882	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr2:34735150-34735189	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr2:34772535-34772743	GM12878	blood:	n/a	n/a
49	CTCF	chr2:34795680-34795830	Caco-2	colon:	n/a	n/a
50	CTCF	chr2:34795659-34795823	SK-N-SH_RA	brain:	n/a	n/a

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:34719565-34719615	AG09309	skin:	n/a
2	chr2:34852273-34852323	AG04450	lung:	fetal
3	chr2:34719565-34719615	AG09309	skin:	n/a
4	chr2:34852273-34852323	AG04450	lung:	fetal
5	chr2:34719565-34719615	T-47D	breast:	n/a
6	chr2:34720275-34720325	SK-N-SH	brain:	n/a
7	chr2:34720275-34720325	Hela-S3	cervix:	n/a
8	chr2:34719719-34719769	HAEpiC	amniotic membrane:	n/a
9	chr2:34719719-34719769	HCT-116	colon:	n/a
10	chr2:34719719-34719769	AG04450	lung:	fetal
11	chr2:34719565-34719615	GM19239	blood:	n/a
12	chr2:34719719-34719769	HepG2	liver:	n/a
13	chr2:34719719-34719769	AG10803	skin:	n/a
14	chr2:34719719-34719769	GM12892	blood:	n/a
15	chr2:34720275-34720325	MCF-7	breast:	n/a
16	chr2:34852273-34852323	HPAEpiC	pulmonary alveolar:	n/a
17	chr2:34719565-34719615	NT2-D1	testis:	n/a
18	chr2:34852273-34852323	ECC-1	luminal epithelium:	n/a
19	chr2:34719719-34719769	HL-60	blood:	n/a
20	chr2:34719565-34719615	SK-N-MC	brain:	n/a
21	chr2:34852273-34852323	SKMC	muscle:	n/a
22	chr2:34719565-34719615	ovcar-3	ovarian:	n/a
23	chr2:34719565-34719615	K562	blood:	n/a
24	chr2:34719565-34719615	NH-A	brain:	n/a
25	chr2:34719565-34719615	HUVEC	blood vessel:	n/a
26	chr2:34719565-34719615	GM12891	blood:	n/a
27	chr2:34719565-34719615	NHDF-neo	bronchial:	n/a
28	chr2:34720275-34720325	GM12892	blood:	n/a
29	chr2:34720275-34720325	HCF	heart:	n/a
30	chr2:34720275-34720325	HRE	kidney:	n/a
31	chr2:34719719-34719769	NB4	blood:	n/a
32	chr2:34720275-34720325	HCT-116	colon:	n/a
33	chr2:34719719-34719769	NHDF-neo	bronchial:	n/a
34	chr2:34719565-34719615	PANC-1	pancreas:	n/a
35	chr2:34719719-34719769	AoSMC	blood vessel:	n/a
36	chr2:34852273-34852323	LNCaP	prostate:	n/a
37	chr2:34719565-34719615	CMK	blood:	n/a
38	chr2:34720275-34720325	Jurkat	blood:	n/a
39	chr2:34719719-34719769	HRPEpiC	eye:	n/a
40	chr2:34852273-34852323	NH-A	brain:	n/a
41	chr2:34719565-34719615	H1-hESC	embryonic stem cell:	embryo
42	chr2:34720275-34720325	HIPEpiC	eye:	n/a
43	chr2:34719719-34719769	PANC-1	pancreas:	n/a
44	chr2:34719719-34719769	HEK293	kidney:	embryo
45	chr2:34719565-34719615	SKMC	muscle:	n/a
46	chr2:34720275-34720325	HUVEC	blood vessel:	n/a
47	chr2:34719719-34719769	SKMC	muscle:	n/a
48	chr2:34719719-34719769	PFSK-1	brain:	n/a
49	chr2:34719719-34719769	PrEC	prostate:	n/a
50	chr2:34852273-34852323	AG09309	skin:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:34321381..34322557-chr2:34795669..34796275,5	MCF-7	breast:
2	chr2:34237681..34238401-chr2:34795339..34796232,5	MCF-7	breast:
3	chr2:34237506..34238447-chr2:34795265..34796658,5	MCF-7	breast:
4	chr2:33906151..33906814-chr2:34795262..34796206,5	MCF-7	breast:
5	chr2:34795663..34796225-chr8:85142407..85143298,2	MCF-7	breast:
6	chr2:34707651..34709954-chr2:34710435..34712219,2	MCF-7	breast:
7	chr2:34321239..34322372-chr2:34772370..34773083,4	MCF-7	breast:
8	chr2:34876891..34879240-chr2:34886043..34888561,2	K562	blood:
9	chr2:34707651..34709954-chr2:34710435..34712219,2	MCF-7	breast:
10	chr2:34876891..34879240-chr2:34886043..34888561,2	K562	blood:
11	chr17:76778253..76778888-chr2:34769758..34770277,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASGRP3-14	chr2:34792150-34792344	NONHSAT070037
2	lnc-RASGRP3-15	chr2:34878421-34878470	NONHSAT070041
3	lnc-RASGRP3-14	chr2:34800570-34801134	NONHSAT070037
4	lnc-RASGRP3-14	chr2:34756150-34756498	NONHSAT070037
5	lnc-RASGRP3-14	chr2:34792147-34792344	l_1807_chr2:34789043-34803561_liver
6	lnc-RASGRP3-14	chr2:34815937-34816109	l_1807_chr2:34789043-34803561_liver
7	lnc-RASGRP3-14	chr2:34800570-34803561	l_1807_chr2:34789043-34803561_liver
8	lnc-RASGRP3-14	chr2:34789044-34789084	l_1807_chr2:34789043-34803561_liver
9	lnc-FAM98A-7	chr2:34787656-34787849	NONHSAT070038
10	lnc-RASGRP3-14	chr2:34811019-34811128	NONHSAT070039
11	lnc-FAM98A-7	chr2:34823138-34823205	NONHSAT070038
12	lnc-RASGRP3-14	chr2:34815892-34816802	NONHSAT070039
13	lnc-RASGRP3-3	chr2:34860316-34860407	ENSG00000226785
14	lnc-RASGRP3-13	chr2:34713820-34713911	NONHSAT070033
15	lnc-RASGRP3-14	chr2:34792161-34792344	NONHSAT070039

No data

Variant related genes	Relation type
ENSG00000228262	TF binding region
ENSG00000228262	CpG island
ENSG00000108669	chromatin interactions

Extended variants
information (count: 2175 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2175 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138735484	chr2:34703158-34703159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs528949694	chr2:34703173-34703174	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs72869750	chr2:34703231-34703232	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs562120550	chr2:34703263-34703264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531163584	chr2:34703275-34703276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551293610	chr2:34703276-34703277	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539864463	chr2:34703301-34703302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148999111	chr2:34703307-34703308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540146199	chr2:34703325-34703326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116004605	chr2:34703356-34703357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566878414	chr2:34703367-34703368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184005266	chr2:34703405-34703406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555862101	chr2:34703421-34703422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs143825617	chr2:34703431-34703432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148130125	chr2:34703436-34703437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs376714850	chr2:34703447-34703448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188651845	chr2:34703476-34703477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191031373	chr2:34703488-34703489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540153945	chr2:34703592-34703593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35086480	chr2:34703599-34703600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs202076573	chr2:34703601-34703602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs397872434	chr2:34703611-34703612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs202150685	chr2:34703612-34703613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141352853	chr2:34703613-34703614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146930320	chr2:34703614-34703615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559867052	chr2:34703715-34703716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573610574	chr2:34703720-34703721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182375622	chr2:34703721-34703722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542343529	chr2:34703725-34703726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562649370	chr2:34703779-34703780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573411114	chr2:34703799-34703800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141948130	chr2:34703819-34703820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187160641	chr2:34703862-34703863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566800547	chr2:34703863-34703864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs72869751	chr2:34703877-34703878	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs533637700	chr2:34703944-34703945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547298374	chr2:34703961-34703962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574530507	chr2:34703972-34703973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145135270	chr2:34703978-34703979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535881890	chr2:34704007-34704008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115773139	chr2:34704077-34704078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7592512	chr2:34704078-34704079	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs139366464	chr2:34704088-34704089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141157097	chr2:34704090-34704091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201179684	chr2:34704092-34704093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs56401309	chr2:34704093-34704094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141676927	chr2:34704163-34704164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562440644	chr2:34704177-34704178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs62161860	chr2:34704179-34704180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545255757	chr2:34704216-34704217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Autism	22495309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:34700600-34711800	Weak transcription	Fetal Kidney	kidney
2	chr2:34702600-34703400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:34703400-34706000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:34706000-34706200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:34706200-34708000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr2:34708000-34708600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:34711000-34712800	Enhancers	Fetal Intestine Large	intestine
8	chr2:34711800-34712200	Enhancers	Fetal Kidney	kidney
9	chr2:34712000-34713000	Enhancers	Fetal Lung	lung
10	chr2:34712800-34717800	Weak transcription	Fetal Intestine Large	intestine
11	chr2:34713000-34714600	Weak transcription	Fetal Lung	lung
12	chr2:34714600-34715000	Enhancers	Fetal Lung	lung
13	chr2:34715000-34716600	Weak transcription	Fetal Lung	lung
14	chr2:34716600-34717200	Enhancers	Fetal Lung	lung
15	chr2:34717200-34717600	Weak transcription	Fetal Lung	lung
16	chr2:34717600-34717800	Enhancers	Fetal Lung	lung
17	chr2:34717800-34718000	Flanking Active TSS	Fetal Lung	lung
18	chr2:34717800-34718400	Enhancers	Fetal Intestine Large	intestine
19	chr2:34718000-34718200	Enhancers	Fetal Lung	lung
20	chr2:34718200-34718400	Flanking Active TSS	Fetal Lung	lung
21	chr2:34718400-34719000	Enhancers	Fetal Lung	lung
22	chr2:34719000-34720800	Weak transcription	Fetal Lung	lung
23	chr2:34720800-34721200	Enhancers	Fetal Lung	lung
24	chr2:34744400-34744600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:34744800-34746000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:34749200-34749600	Enhancers	NHEK	skin
27	chr2:34749200-34749800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr2:34752200-34752400	Enhancers	Fetal Kidney	kidney
29	chr2:34752400-34753200	Weak transcription	Fetal Kidney	kidney
30	chr2:34752800-34753200	Enhancers	Fetal Intestine Large	intestine
31	chr2:34753200-34753600	Enhancers	Fetal Intestine Small	intestine
32	chr2:34753200-34753600	Enhancers	Fetal Kidney	kidney
33	chr2:34753400-34753800	Enhancers	Fetal Intestine Large	intestine
34	chr2:34753600-34758800	Weak transcription	Fetal Kidney	kidney
35	chr2:34753600-34759000	Weak transcription	Fetal Intestine Small	intestine
36	chr2:34758800-34759200	Enhancers	Fetal Kidney	kidney
37	chr2:34758800-34760600	Enhancers	Fetal Lung	lung
38	chr2:34759000-34760600	Enhancers	Fetal Intestine Small	intestine
39	chr2:34759200-34759400	Weak transcription	Fetal Kidney	kidney
40	chr2:34759200-34761400	Enhancers	Fetal Intestine Large	intestine
41	chr2:34759400-34759800	Enhancers	Fetal Kidney	kidney
42	chr2:34761200-34761600	Enhancers	Pancreas	Pancrea
43	chr2:34770400-34771000	Enhancers	Fetal Muscle Trunk	muscle
44	chr2:34772200-34772400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr2:34772400-34773000	Enhancers	Pancreas	Pancrea
46	chr2:34772400-34774200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr2:34773000-34773400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr2:34774000-34775000	Enhancers	NHEK	skin
49	chr2:34774200-34775400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr2:34774200-34775400	Enhancers	HMEC	breast

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