Variant report

Variant	esv3354779
Chromosome Location	chr2:234474774-234478122
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:462)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	ATF3	chr2:234475068-234475632	A549	lung:	n/a	n/a
4	BACH1	chr2:234475144-234475550	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr2:234474395-234475621	A549	lung:	n/a	chr2:234475543-234475556 chr2:234474817-234474826 chr2:234475463-234475476
6	BCL3	chr2:234474862-234475661	A549	lung:	n/a	chr2:234475543-234475556 chr2:234475463-234475476
7	BCLAF1	chr2:234475180-234475695	GM12878	blood:	n/a	chr2:234475543-234475556 chr2:234475463-234475476
8	BHLHE40	chr2:234474978-234475601	K562	blood:	n/a	n/a
9	BHLHE40	chr2:234475310-234475515	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:234474372-234474782	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:234475109-234475603	HepG2	liver:	n/a	n/a
12	BRCA1	chr2:234475147-234475417	HepG2	liver:	n/a	n/a
13	CBX3	chr2:234475220-234475608	K562	blood:	n/a	n/a
14	CBX3	chr2:234475002-234475717	HCT-116	colon:	n/a	n/a
15	CCNT2	chr2:234475023-234475568	K562	blood:	n/a	n/a
16	CEBPB	chr2:234475303-234475493	K562	blood:	n/a	n/a
17	CEBPB	chr2:234475193-234475666	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr2:234475177-234475567	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPD	chr2:234475114-234475658	HepG2	liver:	n/a	n/a
20	CHD1	chr2:234474588-234475413	GM12878	blood:	n/a	n/a
21	CHD2	chr2:234474605-234475617	GM12878	blood:	n/a	n/a
22	CHD2	chr2:234475209-234475512	K562	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	CREB1	chr2:234475048-234475664	A549	lung:	n/a	n/a
28	CREB1	chr2:234474666-234475695	HepG2	liver:	n/a	n/a
29	CREB1	chr2:234475333-234475540	A549	lung:	n/a	n/a
30	CREB1	chr2:234475086-234475670	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr2:234475326-234475525	K562	blood:	n/a	n/a
32	CTCF	chr2:234475448-234475488	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr2:234475266-234475303	GM19239	blood:	n/a	n/a
34	CTCF	chr2:234475260-234475410	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr2:234475120-234475270	GM06990	blood:	n/a	n/a
36	CTCF	chr2:234475186-234475213	GM12878	blood:	n/a	n/a
37	CTCF	chr2:234475174-234475297	GM12892	blood:	n/a	n/a
38	CTCF	chr2:234475199-234475213	GM12891	blood:	n/a	n/a
39	CTCF	chr2:234475222-234475228	MCF-7	breast:	n/a	n/a
40	CTCF	chr2:234475140-234475290	AG04449	skin:	n/a	n/a
41	CTCF	chr2:234475179-234475261	MCF-7	breast:	n/a	n/a
42	CTCF	chr2:234477247-234477295	GM20000	blood:	n/a	n/a
43	CTCF	chr2:234475060-234475210	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr2:234475100-234475250	AG04449	skin:	n/a	n/a
45	CTCF	chr2:234475460-234475610	HMEC	breast:	n/a	n/a
46	CTCF	chr2:234475340-234475490	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr2:234475480-234475630	AG10803	skin:	n/a	n/a
48	CTCF	chr2:234475161-234475284	Fibrobl	skin:	n/a	n/a
49	CTCF	chr2:234474980-234475130	HAc	cerebellar:	n/a	n/a
50	CTCF	chr2:234475120-234475270	SK-N-SH_RA	brain:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr2:234452682..234455147-chr2:234473464..234475374,2	MCF-7	breast:
2	chr2:234472403..234474529-chr2:234475981..234478934,2	MCF-7	breast:
3	chr2:234393753..234400835-chr2:234472864..234476478,8	MCF-7	breast:
4	chr2:234400872..234402381-chr2:234473582..234476254,2	MCF-7	breast:
5	chr2:234473282..234477495-chr2:234598048..234603332,9	MCF-7	breast:
6	chr2:234473931..234475939-chr2:234762064..234763860,2	K562	blood:
7	chr2:234389092..234391362-chr2:234473035..234476486,3	MCF-7	breast:
8	chr2:234475015..234475516-chr20:34205146..34205692,2	NB4	blood:
9	chr2:234474046..234476375-chr2:234618981..234621894,3	MCF-7	breast:
10	chr2:234472037..234477650-chr2:234599067..234602356,8	MCF-7	breast:
11	chr2:234475954..234478927-chr2:234479708..234482579,2	MCF-7	breast:

No data

Variant related genes	Relation type
USP40	TF binding region
ENSG00000271639	chromatin interactions
ENSG00000085982	chromatin interactions
ENSG00000061656	chromatin interactions
ENSG00000240224	chromatin interactions
ENSG00000167165	chromatin interactions
ENSG00000123485	chromatin interactions

Extended variants
information (count: 110 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:110 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541601477	chr2:234474801-234474802	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs147624581	chr2:234474808-234474809	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs142426540	chr2:234474821-234474822	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs537472487	chr2:234474825-234474826	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs73996138	chr2:234474874-234474875	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs35722741	chr2:234474899-234474900	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs567993279	chr2:234474921-234474922	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs561718296	chr2:234474950-234474951	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs4663710	chr2:234474956-234474957	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs144772512	chr2:234474986-234474987	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs12994878	chr2:234474990-234474991	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs112047382	chr2:234475010-234475011	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs557457761	chr2:234475038-234475039	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs150151167	chr2:234475058-234475059	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs111249647	chr2:234475070-234475071	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs543447183	chr2:234475107-234475108	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs111942439	chr2:234475119-234475120	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs112793557	chr2:234475120-234475121	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs529192171	chr2:234475193-234475194	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs542517424	chr2:234475224-234475225	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs554326385	chr2:234475229-234475230	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs143663553	chr2:234475234-234475235	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs112852283	chr2:234475235-234475236	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs571329361	chr2:234475282-234475283	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs77550906	chr2:234475297-234475298	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs377522114	chr2:234475331-234475332	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs377485271	chr2:234475371-234475372	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs189252815	chr2:234475372-234475373	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs191251401	chr2:234475381-234475382	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs183752976	chr2:234475393-234475394	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs113463832	chr2:234475408-234475409	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs62192778	chr2:234475415-234475416	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs566801128	chr2:234475435-234475436	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs148158811	chr2:234475440-234475441	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs558715849	chr2:234475483-234475484	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs577365835	chr2:234475505-234475506	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs537215148	chr2:234475537-234475538	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs536701187	chr2:234475558-234475559	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs556927952	chr2:234475568-234475569	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs573523486	chr2:234475573-234475574	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs542932313	chr2:234475596-234475597	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs559713330	chr2:234475606-234475607	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs557068522	chr2:234475642-234475643	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs186935219	chr2:234475650-234475651	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs542792250	chr2:234475684-234475685	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs71058564	chr2:234475708-234475709	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs66727805	chr2:234475735-234475736	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs71359949	chr2:234475851-234475852	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs71359948	chr2:234475877-234475878	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs372538075	chr2:234475903-234475904	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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

Chromatin state (count:187 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234432200-234474800	Weak transcription	Spleen	Spleen
2	chr2:234441600-234474800	Weak transcription	Gastric	stomach
3	chr2:234447800-234474800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr2:234466400-234474800	Weak transcription	Esophagus	oesophagus
5	chr2:234466600-234474800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr2:234474000-234474800	Flanking Active TSS	Dnd41	blood
7	chr2:234474000-234475600	Active TSS	Fetal Brain Male	brain
8	chr2:234474000-234475800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr2:234474000-234475800	Active TSS	Right Atrium	heart
10	chr2:234474000-234475800	Active TSS	Stomach Smooth Muscle	stomach
11	chr2:234474200-234474800	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr2:234474200-234474800	Active TSS	Primary B cells from cord blood	blood
13	chr2:234474200-234474800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
14	chr2:234474200-234475000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr2:234474200-234475200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr2:234474200-234475400	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr2:234474200-234475600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr2:234474200-234475600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr2:234474200-234475800	Active TSS	HUES64 Cell Line	embryonic stem cell
20	chr2:234474200-234475800	Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr2:234474200-234475800	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr2:234474200-234475800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr2:234474200-234475800	Active TSS	Fetal Intestine Small	intestine
24	chr2:234474200-234475800	Active TSS	Psoas Muscle	Psoas
25	chr2:234474200-234475800	Active TSS	Thymus	Thymus
26	chr2:234474400-234474800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr2:234474400-234474800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
28	chr2:234474400-234474800	Flanking Active TSS	Primary T cells from cord blood	blood
29	chr2:234474400-234474800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
30	chr2:234474400-234474800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
31	chr2:234474400-234474800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
32	chr2:234474400-234474800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
33	chr2:234474400-234474800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
34	chr2:234474400-234474800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr2:234474400-234474800	Flanking Active TSS	Duodenum Mucosa	Duodenum
36	chr2:234474400-234474800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
37	chr2:234474400-234474800	Active TSS	HepG2	liver
38	chr2:234474400-234475000	Flanking Active TSS	Primary hematopoietic stem cells	blood
39	chr2:234474400-234475000	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
40	chr2:234474400-234475000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
41	chr2:234474400-234475000	Flanking Active TSS	Brain Germinal Matrix	brain
42	chr2:234474400-234475000	Flanking Active TSS	HUVEC	blood vessel
43	chr2:234474400-234475200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr2:234474400-234475400	Active TSS	Aorta	Aorta
45	chr2:234474400-234475400	Active TSS	Liver	Liver
46	chr2:234474400-234475400	Active TSS	Fetal Heart	heart
47	chr2:234474400-234475600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr2:234474400-234475600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr2:234474400-234475600	Active TSS	Colon Smooth Muscle	Colon
50	chr2:234474400-234475600	Active TSS	Duodenum Smooth Muscle	Duodenum

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