Variant report

Variant	nsv584672
Chromosome Location	chr2:231289976-231348888
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	chr2:231290097-231290451	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:231304365-231304808	K562	blood:	n/a	n/a
3	ATF1	chr2:231323998-231324175	K562	blood:	n/a	n/a
4	ATF2	chr2:231312481-231313264	GM12878	blood:	n/a	n/a
5	ATF2	chr2:231336631-231337934	GM12878	blood:	n/a	n/a
6	ATF2	chr2:231312367-231313329	GM12878	blood:	n/a	n/a
7	ATF2	chr2:231335675-231336465	GM12878	blood:	n/a	n/a
8	ATF2	chr2:231335736-231336608	GM12878	blood:	n/a	n/a
9	ATF2	chr2:231337026-231337690	GM12878	blood:	n/a	n/a
10	ATF3	chr2:231289996-231290587	HCT-116	colon:	n/a	n/a
11	ATF3	chr2:231294360-231294570	K562	blood:	n/a	n/a
12	BATF	chr2:231308261-231308589	GM12878	blood:	n/a	n/a
13	BATF	chr2:231312538-231313109	GM12878	blood:	n/a	n/a
14	BATF	chr2:231337322-231337682	GM12878	blood:	n/a	n/a
15	BATF	chr2:231337273-231337705	GM12878	blood:	n/a	n/a
16	BATF	chr2:231312448-231313156	GM12878	blood:	n/a	n/a
17	BATF	chr2:231295941-231296275	GM12878	blood:	n/a	n/a
18	BCL11A	chr2:231312449-231313145	GM12878	blood:	n/a	chr2:231312984-231312993
19	BCL11A	chr2:231312471-231313197	GM12878	blood:	n/a	chr2:231312984-231312993
20	BCL11A	chr2:231337281-231337711	GM12878	blood:	n/a	n/a
21	BCL3	chr2:231336969-231338509	GM12878	blood:	n/a	chr2:231338274-231338283
22	BCL3	chr2:231336965-231337410	GM12878	blood:	n/a	n/a
23	BCLAF1	chr2:231335664-231338387	GM12878	blood:	n/a	chr2:231335975-231335984 chr2:231338274-231338283
24	BCLAF1	chr2:231337169-231337854	GM12878	blood:	n/a	n/a
25	BCLAF1	chr2:231312207-231313273	GM12878	blood:	n/a	chr2:231312984-231312993
26	BHLHE40	chr2:231311859-231311984	GM12878	blood:	n/a	n/a
27	BHLHE40	chr2:231337268-231337612	GM12878	blood:	n/a	n/a
28	BHLHE40	chr2:231335905-231336128	GM12878	blood:	n/a	n/a
29	BHLHE40	chr2:231312514-231313149	GM12878	blood:	n/a	n/a
30	CBX3	chr2:231294294-231294533	K562	blood:	n/a	n/a
31	CBX3	chr2:231294240-231294571	K562	blood:	n/a	n/a
32	CEBPB	chr2:231289708-231290476	Hela-S3	cervix:	n/a	chr2:231290285-231290296 chr2:231290257-231290268
33	CEBPB	chr2:231290077-231290476	HepG2	liver:	n/a	chr2:231290285-231290296 chr2:231290257-231290268
34	CEBPB	chr2:231306021-231306142	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:231305905-231306269	IMR90	lung:	n/a	n/a
36	CEBPB	chr2:231289998-231290477	A549	lung:	n/a	chr2:231290285-231290296 chr2:231290257-231290268
37	CEBPB	chr2:231290038-231290562	HCT-116	colon:	n/a	chr2:231290285-231290296 chr2:231290257-231290268
38	CEBPB	chr2:231347676-231347921	HepG2	liver:	n/a	chr2:231347799-231347810
39	CEBPB	chr2:231337413-231337647	IMR90	lung:	n/a	n/a
40	CEBPB	chr2:231312354-231313330	GM12878	blood:	n/a	n/a
41	CEBPB	chr2:231337229-231337878	HCT-116	colon:	n/a	n/a
42	CEBPB	chr2:231290146-231290424	HepG2	liver:	n/a	chr2:231290285-231290296 chr2:231290257-231290268
43	CEBPB	chr2:231290113-231290427	H1-hESC	embryonic stem cell:	n/a	chr2:231290285-231290296 chr2:231290257-231290268
44	CEBPB	chr2:231296517-231296794	A549	lung:	n/a	chr2:231296675-231296686
45	CEBPB	chr2:231290108-231290474	IMR90	lung:	n/a	chr2:231290285-231290296 chr2:231290257-231290268
46	CEBPB	chr2:231290108-231290459	A549	lung:	n/a	chr2:231290285-231290296 chr2:231290257-231290268
47	CEBPB	chr2:231296606-231296806	HepG2	liver:	n/a	chr2:231296675-231296686
48	CEBPB	chr2:231290100-231290446	K562	blood:	n/a	chr2:231290285-231290296 chr2:231290257-231290268
49	CEBPB	chr2:231289918-231290641	HCT-116	colon:	n/a	chr2:231290285-231290296 chr2:231290257-231290268
50	CEBPB	chr2:231299713-231299900	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:231292538..231294481-chr2:231296782..231298607,2	MCF-7	breast:
2	chr2:231292538..231294481-chr2:231296782..231298607,2	MCF-7	breast:
3	chr2:231292379..231294379-chr2:231300867..231302513,2	K562	blood:
4	chr2:231279705..231282048-chr2:231316333..231318680,2	K562	blood:
5	chr2:231280204..231284388-chr2:231286093..231293391,7	K562	blood:
6	chr2:231311040..231312950-chr2:231322465..231324120,2	K562	blood:
7	chr2:231299092..231301889-chr2:231304564..231307133,2	K562	blood:
8	chr2:231320643..231324421-chr2:231326944..231329739,3	K562	blood:
9	chr2:231292379..231294379-chr2:231300867..231302513,2	K562	blood:
10	chr2:231321959..231324583-chr2:231327145..231329217,3	K562	blood:
11	chr2:231299092..231300895-chr2:231303797..231306064,2	K562	blood:
12	chr2:231299092..231301889-chr2:231304564..231307133,2	K562	blood:
13	chr2:231280204..231282363-chr2:231291023..231293391,2	K562	blood:
14	chr2:231278566..231281205-chr2:231316961..231318680,2	K562	blood:
15	chr2:231281967..231284273-chr2:231304753..231307439,2	K562	blood:
16	chr2:231311040..231312950-chr2:231322465..231324120,2	K562	blood:
17	chr2:36824809..36825682-chr2:231297731..231298446,2	NB4	blood:
18	chr2:231312551..231315093-chr2:231315944..231317572,2	MCF-7	breast:
19	chr2:231323177..231324893-chr2:231325884..231328620,2	MCF-7	breast:
20	chr2:231299092..231300895-chr2:231303797..231306064,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SP140L-4	chr2:231333547-231333811	NONHSAT077287
2	lnc-SP140L-4	chr2:231334730-231335075	NONHSAT077287
3	lnc-SP140L-3	chr2:231331016-231331069	NONHSAT077285
4	lnc-SP140L-5	chr2:231339109-231339162	NONHSAT077289
5	lnc-SP140L-5	chr2:231337832-231338155	NONHSAT077289
6	lnc-SP140L-3	chr2:231331835-231331862	NONHSAT077285
7	lnc-SP140L-3	chr2:231328333-231328865	NONHSAT077285
8	lnc-SP110-7	chr2:231330481-231330918	NONHSAT077286
9	lnc-SP140L-4	chr2:231333758-231333811	NONHSAT077284
10	lnc-SP140L-4	chr2:231334730-231335232	NONHSAT077284

Variant related genes	Relation type
SP100	TF binding region
ENSG00000067066	chromatin interactions
ENSG00000171055	chromatin interactions

Extended variants
information (count: 2229 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2229 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12694867	chr2:231289976-231289977	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs533076043	chr2:231290021-231290022	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs181212269	chr2:231290026-231290027	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs111411726	chr2:231290112-231290113	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs530423848	chr2:231290152-231290153	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs186195832	chr2:231290166-231290167	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs542024719	chr2:231290179-231290180	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs528292991	chr2:231290230-231290231	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs149511599	chr2:231290247-231290248	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs189160503	chr2:231290258-231290259	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs539960175	chr2:231290260-231290261	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs375453116	chr2:231290300-231290301	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs200784019	chr2:231290303-231290304	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs143997587	chr2:231290328-231290329	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs528210204	chr2:231290402-231290403	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs570065947	chr2:231290424-231290425	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs537399357	chr2:231290457-231290458	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs540392825	chr2:231290516-231290517	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs35350531	chr2:231290517-231290518	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs397687978	chr2:231290527-231290528	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs556108725	chr2:231290547-231290548	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs574245413	chr2:231290549-231290550	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs545104914	chr2:231290599-231290600	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs148284006	chr2:231290603-231290604	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs141343406	chr2:231290613-231290614	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs544751923	chr2:231290614-231290615	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs182556756	chr2:231290615-231290616	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs574903281	chr2:231290721-231290722	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs542183662	chr2:231290741-231290742	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs560872102	chr2:231290768-231290769	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs146310446	chr2:231290910-231290911	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs546565184	chr2:231290914-231290915	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs565131643	chr2:231290989-231290990	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs532158118	chr2:231291004-231291005	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs139497837	chr2:231291041-231291042	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs186301085	chr2:231291053-231291054	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs537462294	chr2:231291079-231291080	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs144182801	chr2:231291124-231291125	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs2396758	chr2:231291144-231291145	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs190654168	chr2:231291164-231291165	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201151945	chr2:231291240-231291241	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs3028414	chr2:231291241-231291242	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs151324586	chr2:231291242-231291243	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs113177927	chr2:231291243-231291244	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs199606726	chr2:231291244-231291245	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs397829082	chr2:231291245-231291246	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs567610848	chr2:231291253-231291254	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs182940391	chr2:231291256-231291257	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs146098214	chr2:231291287-231291288	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs7355772	chr2:231291290-231291291	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Chronic lymphocytic leukemia	21546498	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
Breast cancer	22522925	CNVD

Chromatin state (count:1976 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231281600-231294800	Weak transcription	Gastric	stomach
2	chr2:231281800-231293000	Weak transcription	Fetal Stomach	stomach
3	chr2:231282000-231293400	Weak transcription	Fetal Muscle Trunk	muscle
4	chr2:231282000-231294000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr2:231282400-231292600	Weak transcription	A549	lung
6	chr2:231282600-231290000	Weak transcription	Placenta	Placenta
7	chr2:231283600-231293800	Weak transcription	Fetal Lung	lung
8	chr2:231283600-231294800	Weak transcription	HSMM	muscle
9	chr2:231283600-231309200	Weak transcription	Stomach Smooth Muscle	stomach
10	chr2:231283800-231294600	Weak transcription	Fetal Heart	heart
11	chr2:231283800-231294800	Weak transcription	Esophagus	oesophagus
12	chr2:231284200-231290400	Genic enhancers	Primary B cells from peripheral blood	blood
13	chr2:231284200-231290400	Genic enhancers	Monocytes-CD14+_RO01746	blood
14	chr2:231284200-231290800	Weak transcription	Hela-S3	cervix
15	chr2:231284200-231292000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr2:231284200-231292200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr2:231284200-231292400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr2:231284200-231294800	Weak transcription	Lung	lung
19	chr2:231284200-231294800	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr2:231284200-231294800	Weak transcription	Thymus	Thymus
21	chr2:231284200-231301000	Weak transcription	Rectal Smooth Muscle	rectum
22	chr2:231284200-231304000	Weak transcription	NH-A	brain
23	chr2:231284400-231293000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr2:231284600-231306200	Weak transcription	HMEC	breast
25	chr2:231285200-231290400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr2:231285400-231290400	Genic enhancers	Primary B cells from cord blood	blood
27	chr2:231287600-231291600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr2:231287600-231292200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr2:231287600-231293400	Weak transcription	Fetal Muscle Leg	muscle
30	chr2:231287800-231292400	Enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr2:231288400-231290800	Enhancers	HepG2	liver
32	chr2:231288600-231290400	Genic enhancers	Primary T cells fromperipheralblood	blood
33	chr2:231288800-231290000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr2:231288800-231290200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr2:231288800-231290600	Genic enhancers	Primary T cells from cord blood	blood
36	chr2:231288800-231290600	Weak transcription	HUVEC	blood vessel
37	chr2:231288800-231293800	Weak transcription	NHDF-Ad	bronchial
38	chr2:231288800-231319000	Weak transcription	Fetal Kidney	kidney
39	chr2:231288800-231356000	Weak transcription	Stomach Mucosa	stomach
40	chr2:231289000-231290000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr2:231289000-231290000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr2:231289000-231290000	Enhancers	Liver	Liver
43	chr2:231289000-231290200	Weak transcription	NHEK	skin
44	chr2:231289000-231290400	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr2:231289000-231290400	Weak transcription	K562	blood
46	chr2:231289000-231291600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr2:231289000-231291600	Weak transcription	Dnd41	blood
48	chr2:231289000-231291800	Weak transcription	Fetal Intestine Small	intestine
49	chr2:231289000-231292000	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr2:231289000-231292200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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