Variant report

Variant	nsv519876
Chromosome Location	chr2:234466843-234493048
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:535)
CpG islands
(count:0)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:535 , 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	ARID3A	chr2:234475265-234475676	K562	blood:	n/a	n/a
2	ARID3A	chr2:234475017-234475641	HepG2	liver:	n/a	n/a
3	ATF1	chr2:234483767-234483892	K562	blood:	n/a	n/a
4	ATF1	chr2:234472775-234473093	K562	blood:	n/a	n/a
5	ATF3	chr2:234475068-234475632	A549	lung:	n/a	n/a
6	BACH1	chr2:234475144-234475550	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr2:234474862-234475661	A549	lung:	n/a	chr2:234475543-234475556 chr2:234475463-234475476
8	BCL3	chr2:234474395-234475621	A549	lung:	n/a	chr2:234475543-234475556 chr2:234474817-234474826 chr2:234475463-234475476
9	BCLAF1	chr2:234475180-234475695	GM12878	blood:	n/a	chr2:234475543-234475556 chr2:234475463-234475476
10	BHLHE40	chr2:234474978-234475601	K562	blood:	n/a	n/a
11	BHLHE40	chr2:234474372-234474782	GM12878	blood:	n/a	n/a
12	BHLHE40	chr2:234475310-234475515	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:234475109-234475603	HepG2	liver:	n/a	n/a
14	BRCA1	chr2:234475147-234475417	HepG2	liver:	n/a	n/a
15	CBX3	chr2:234475002-234475717	HCT-116	colon:	n/a	n/a
16	CBX3	chr2:234475220-234475608	K562	blood:	n/a	n/a
17	CCNT2	chr2:234475023-234475568	K562	blood:	n/a	n/a
18	CEBPB	chr2:234475303-234475493	K562	blood:	n/a	n/a
19	CEBPB	chr2:234475193-234475666	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr2:234475177-234475567	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPD	chr2:234475114-234475658	HepG2	liver:	n/a	n/a
22	CHD1	chr2:234474588-234475413	GM12878	blood:	n/a	n/a
23	CHD2	chr2:234475093-234475547	HepG2	liver:	n/a	n/a
24	CHD2	chr2:234475194-234475640	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr2:234474405-234475666	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr2:234474858-234474867	K562	blood:	n/a	n/a
27	CHD2	chr2:234474605-234475617	GM12878	blood:	n/a	n/a
28	CHD2	chr2:234475209-234475512	K562	blood:	n/a	n/a
29	CREB1	chr2:234475333-234475540	A549	lung:	n/a	n/a
30	CREB1	chr2:234474666-234475695	HepG2	liver:	n/a	n/a
31	CREB1	chr2:234475048-234475664	A549	lung:	n/a	n/a
32	CREB1	chr2:234475086-234475670	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr2:234485826-234485913	Lung_OC	lung:	n/a	n/a
34	CTCF	chr2:234475326-234475525	K562	blood:	n/a	n/a
35	CTCF	chr2:234475161-234475284	Fibrobl	skin:	n/a	n/a
36	CTCF	chr2:234475222-234475228	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:234475460-234475610	HMEC	breast:	n/a	n/a
38	CTCF	chr2:234475174-234475297	GM12892	blood:	n/a	n/a
39	CTCF	chr2:234475448-234475488	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr2:234475060-234475210	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr2:234475186-234475213	GM12878	blood:	n/a	n/a
42	CTCF	chr2:234475120-234475270	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr2:234475140-234475290	AG04449	skin:	n/a	n/a
44	CTCF	chr2:234475340-234475490	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr2:234475100-234475250	AG04449	skin:	n/a	n/a
46	CTCF	chr2:234475266-234475303	GM19239	blood:	n/a	n/a
47	CTCF	chr2:234481120-234481270	GM12869	blood:	n/a	n/a
48	CTCF	chr2:234475260-234475410	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr2:234475480-234475630	AG10803	skin:	n/a	n/a
50	CTCF	chr2:234475179-234475261	MCF-7	breast:	n/a	n/a

No data

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:234392005..234393999-chr2:234465226..234467759,2	MCF-7	breast:
2	chr2:234475954..234478927-chr2:234479708..234482579,2	MCF-7	breast:
3	chr2:234475015..234475516-chr20:34205146..34205692,2	NB4	blood:
4	chr2:234347642..234349247-chr2:234472522..234474070,2	K562	blood:
5	chr2:234452682..234455147-chr2:234473464..234475374,2	MCF-7	breast:
6	chr2:234465036..234467198-chr2:234467958..234469567,2	K562	blood:
7	chr2:234473282..234477495-chr2:234598048..234603332,9	MCF-7	breast:
8	chr2:234470715..234472722-chr2:234612737..234614853,2	MCF-7	breast:
9	chr2:234472403..234474529-chr2:234475981..234478934,2	MCF-7	breast:
10	chr2:234475176..234476679-chr2:234491140..234493711,2	MCF-7	breast:
11	chr2:234473931..234475939-chr2:234762064..234763860,2	K562	blood:
12	chr2:234474046..234476375-chr2:234618981..234621894,3	MCF-7	breast:
13	chr2:234466977..234469529-chr2:234473794..234475392,2	K562	blood:
14	chr2:234464618..234469702-chr2:234598682..234603333,7	MCF-7	breast:
15	chr2:234394050..234398896-chr2:234464004..234468219,7	MCF-7	breast:
16	chr2:234468847..234471502-chr2:234600435..234602323,2	MCF-7	breast:
17	chr2:234389092..234391362-chr2:234473035..234476486,3	MCF-7	breast:
18	chr2:234475954..234478927-chr2:234479708..234482579,2	MCF-7	breast:
19	2:234492023-234494396..2:234954947-234965240	Hela-S3	cervix:
20	chr2:234472035..234473937-chr2:234616865..234619680,2	MCF-7	breast:
21	chr2:234472037..234477650-chr2:234599067..234602356,8	MCF-7	breast:
22	chr2:234461453..234463034-chr2:234464749..234466939,2	K562	blood:
23	chr2:234464216..234467169-chr2:234597494..234599447,2	MCF-7	breast:
24	chr2:234400872..234402381-chr2:234473582..234476254,2	MCF-7	breast:
25	2:234492023-234494396..2:234543708-234558325	GM12878	blood:
26	2:234492023-234494396..2:234743181-234749667	Hela-S3	cervix:
27	chr2:234463856..234470010-chr2:234471624..234476696,15	MCF-7	breast:
28	chr2:234465521..234470756-chr2:234471453..234476730,10	MCF-7	breast:
29	chr2:234460739..234462307-chr2:234463991..234467615,3	K562	blood:
30	chr2:234465036..234467198-chr2:234467958..234469567,2	K562	blood:
31	chr2:234464967..234466988-chr2:234593051..234595705,2	MCF-7	breast:
32	chr2:234395132..234400709-chr2:234463204..234468540,10	MCF-7	breast:
33	chr2:234393753..234400835-chr2:234472864..234476478,8	MCF-7	breast:
34	chr2:234467119..234468871-chr2:234606248..234608879,2	MCF-7	breast:
35	chr2:234468108..234469829-chr2:234620038..234622654,2	MCF-7	breast:
36	chr2:234428819..234430328-chr2:234465881..234468297,2	MCF-7	breast:
37	chr2:234465964..234468477-chr2:234472532..234475294,2	K562	blood:

No data

Variant related genes	Relation type
USP40	TF binding region
UGT1A12P	TF binding region
ENSG00000123485	chromatin interactions
ENSG00000061656	chromatin interactions
ENSG00000072080	chromatin interactions
ENSG00000085982	chromatin interactions
ENSG00000271639	chromatin interactions
ENSG00000242515	chromatin interactions
ENSG00000224814	chromatin interactions
ENSG00000167165	chromatin interactions
ENSG00000234143	chromatin interactions
ENSG00000240224	chromatin interactions

Extended variants
information (count: 904 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:904 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12472244	chr2:234466843-234466844	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs540788505	chr2:234466869-234466870	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs377190658	chr2:234466882-234466883	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs535005489	chr2:234466898-234466899	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs534097250	chr2:234466933-234466934	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs549405678	chr2:234466941-234466942	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs562939719	chr2:234466945-234466946	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs369795373	chr2:234467018-234467019	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs529155588	chr2:234467025-234467026	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs549219408	chr2:234467100-234467101	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs565752963	chr2:234467160-234467161	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs148571610	chr2:234467169-234467170	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs551267827	chr2:234467182-234467183	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs141946038	chr2:234467200-234467201	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs75667073	chr2:234467266-234467267	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs557394067	chr2:234467272-234467273	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs574040548	chr2:234467278-234467279	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs536557941	chr2:234467299-234467300	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs192084691	chr2:234467302-234467303	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs372947779	chr2:234467335-234467336	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs369966937	chr2:234467405-234467406	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs73996127	chr2:234467417-234467418	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs182746755	chr2:234467440-234467441	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs372952253	chr2:234467471-234467472	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs150733643	chr2:234467472-234467473	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs543068689	chr2:234467486-234467487	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs139212900	chr2:234467505-234467506	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs528825620	chr2:234467510-234467511	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs201644858	chr2:234467526-234467527	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs185841893	chr2:234467535-234467536	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs36062504	chr2:234467593-234467594	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs75376968	chr2:234467645-234467646	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs528362564	chr2:234467646-234467647	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs577715018	chr2:234467647-234467648	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs143974222	chr2:234467697-234467698	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs79994094	chr2:234467708-234467709	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs191097076	chr2:234467791-234467792	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs551058275	chr2:234467823-234467824	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs543255026	chr2:234467837-234467838	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs74432143	chr2:234467850-234467851	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs536675571	chr2:234467888-234467889	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs553076677	chr2:234467901-234467902	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs567194421	chr2:234468028-234468029	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs79479792	chr2:234468042-234468043	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs558727974	chr2:234468064-234468065	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs575394571	chr2:234468103-234468104	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs543130097	chr2:234468142-234468143	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs6720619	chr2:234468148-234468149	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs376347714	chr2:234468191-234468192	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs182531405	chr2:234468215-234468216	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	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
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	22429812	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
prenatal diagnosis	22389664	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mental retardation	20152051	CNVD
Cancer	21183584	CNVD
Albright''s disease	22277900	CNVD
Brachydactyly-Mental Retardation Syndrome	22470819	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Colorectal cancer	19359472	CNVD
Autism	18414403	CNVD
Chronic myeloid leukemia	21384125	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:606 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234402200-234472400	Weak transcription	Psoas Muscle	Psoas
2	chr2:234413000-234474200	Weak transcription	Fetal Heart	heart
3	chr2:234423200-234473400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr2:234426200-234474000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:234428800-234474400	Weak transcription	Brain Germinal Matrix	brain
6	chr2:234430200-234473800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr2:234430800-234472800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr2:234432000-234467600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr2:234432200-234474800	Weak transcription	Spleen	Spleen
10	chr2:234432600-234474400	Weak transcription	Colonic Mucosa	Colon
11	chr2:234437200-234474400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:234441600-234474800	Weak transcription	Gastric	stomach
13	chr2:234442400-234474400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr2:234447800-234474800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr2:234451200-234474200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr2:234453200-234474400	Weak transcription	Small Intestine	intestine
17	chr2:234453600-234474000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr2:234455400-234468400	Weak transcription	Fetal Intestine Small	intestine
19	chr2:234455400-234474400	Weak transcription	Brain Cingulate Gyrus	brain
20	chr2:234456600-234474000	Weak transcription	Fetal Brain Male	brain
21	chr2:234457400-234474000	Weak transcription	Rectal Smooth Muscle	rectum
22	chr2:234459200-234469800	Strong transcription	Liver	Liver
23	chr2:234459600-234470000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr2:234459800-234469200	Strong transcription	HepG2	liver
25	chr2:234460000-234469800	Strong transcription	Adipose Nuclei	Adipose
26	chr2:234460600-234474000	Weak transcription	Colon Smooth Muscle	Colon
27	chr2:234461400-234469600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr2:234461800-234474000	Weak transcription	Primary T helper cells PMA-I stimulated	--
29	chr2:234462400-234467600	Weak transcription	Fetal Kidney	kidney
30	chr2:234462600-234467400	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr2:234462800-234467200	Weak transcription	Fetal Lung	lung
32	chr2:234463000-234474200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr2:234463200-234467200	Weak transcription	Primary B cells from cord blood	blood
34	chr2:234463200-234467200	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr2:234463200-234473400	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr2:234464200-234467400	Strong transcription	Fetal Stomach	stomach
37	chr2:234464800-234468600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr2:234464800-234469600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr2:234465000-234469600	Strong transcription	Stomach Smooth Muscle	stomach
40	chr2:234465200-234468200	Strong transcription	Rectal Mucosa Donor 31	rectum
41	chr2:234465400-234468000	Strong transcription	Cortex derived primary cultured neurospheres	brain
42	chr2:234465400-234468000	Strong transcription	Rectal Mucosa Donor 29	rectum
43	chr2:234465600-234467000	Enhancers	HSMM	muscle
44	chr2:234465800-234467000	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr2:234465800-234467400	Strong transcription	Left Ventricle	heart
46	chr2:234465800-234468000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr2:234465800-234469200	Strong transcription	Sigmoid Colon	Sigmoid Colon
48	chr2:234465800-234469600	Strong transcription	Duodenum Mucosa	Duodenum
49	chr2:234465800-234472400	Weak transcription	K562	blood
50	chr2:234466000-234467200	Weak transcription	Placenta	Placenta

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