Variant report

Variant	rs34007534
Chromosome Location	chr2:10587570-10587571
allele	C/G
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	POLR2A	chr2:10587465-10588665	GM12878	blood:	n/a	n/a
2	POLR2A	chr2:10587534-10589505	GM12878	blood:	n/a	n/a
3	POLR2A	chr2:10587336-10588652	GM12892	blood:	n/a	n/a
4	POLR2A	chr2:10587540-10587780	HepG2	liver:	n/a	n/a
5	TCF12	chr2:10587325-10588396	A549	lung:	n/a	n/a
6	POLR2A	chr2:10587510-10587927	SK-N-SH	brain:	n/a	n/a
7	POLR2A	chr2:10587357-10587705	K562	blood:	n/a	n/a
8	BACH1	chr2:10587483-10587820	K562	blood:	n/a	n/a
9	MAX	chr2:10587436-10589475	A549	lung:	n/a	chr2:10588126-10588135 chr2:10588941-10588950 chr2:10588939-10588948 chr2:10588651-10588660 chr2:10588126-10588136 chr2:10588125-10588136 chr2:10588939-10588949 chr2:10588496-10588505 chr2:10588124-10588137 chr2:10588938-10588949 chr2:10588125-10588134 chr2:10588938-10588948 chr2:10588125-10588136 chr2:10588938-10588949 chr2:10588930-10588946 chr2:10588939-10588948 chr2:10588500-10588509 chr2:10588125-10588136 chr2:10588124-10588137 chr2:10588939-10588948
10	POLR2A	chr2:10587568-10588702	HL-60	blood:	n/a	n/a
11	SMC3	chr2:10587514-10587915	Hela-S3	cervix:	n/a	n/a
12	BHLHE40	chr2:10587527-10589296	GM12878	blood:	n/a	n/a
13	POLR2A	chr2:10587491-10588673	ECC-1	luminal epithelium:	n/a	n/a
14	CHD2	chr2:10587546-10589316	GM12878	blood:	n/a	n/a
15	E2F6	chr2:10587425-10589683	H1-hESC	embryonic stem cell:	n/a	chr2:10588665-10588674 chr2:10587961-10587970 chr2:10588257-10588267 chr2:10588788-10588797
16	CHD1	chr2:10586760-10588522	GM12878	blood:	n/a	n/a
17	MAX	chr2:10587527-10589593	HepG2	liver:	n/a	chr2:10588126-10588135 chr2:10588941-10588950 chr2:10588939-10588948 chr2:10588651-10588660 chr2:10588126-10588136 chr2:10588125-10588136 chr2:10588939-10588949 chr2:10588496-10588505 chr2:10588124-10588137 chr2:10588938-10588949 chr2:10588125-10588134 chr2:10588938-10588948 chr2:10588125-10588136 chr2:10588938-10588949 chr2:10588930-10588946 chr2:10588939-10588948 chr2:10588500-10588509 chr2:10588125-10588136 chr2:10588124-10588137 chr2:10588939-10588948
18	MYC	chr2:10587414-10589934	K562	blood:	n/a	chr2:10588126-10588135 chr2:10588941-10588950 chr2:10588939-10588948 chr2:10588651-10588660 chr2:10588126-10588136 chr2:10588125-10588136 chr2:10588939-10588949 chr2:10588496-10588505 chr2:10588124-10588137 chr2:10588938-10588949 chr2:10589691-10589701 chr2:10588125-10588134 chr2:10588938-10588948 chr2:10588125-10588136 chr2:10588938-10588949 chr2:10588930-10588946 chr2:10588939-10588948 chr2:10588500-10588509 chr2:10588125-10588136 chr2:10588124-10588137 chr2:10588939-10588948
19	MTA3	chr2:10587452-10588210	GM12878	blood:	n/a	n/a
20	MAX	chr2:10587516-10589455	H1-hESC	embryonic stem cell:	n/a	chr2:10588126-10588135 chr2:10588941-10588950 chr2:10588939-10588948 chr2:10588651-10588660 chr2:10588126-10588136 chr2:10588125-10588136 chr2:10588939-10588949 chr2:10588496-10588505 chr2:10588124-10588137 chr2:10588938-10588949 chr2:10588125-10588134 chr2:10588938-10588948 chr2:10588125-10588136 chr2:10588938-10588949 chr2:10588930-10588946 chr2:10588939-10588948 chr2:10588500-10588509 chr2:10588125-10588136 chr2:10588124-10588137 chr2:10588939-10588948
21	POLR2A	chr2:10587471-10589001	HUVEC	blood vessel:	n/a	n/a
22	POLR2A	chr2:10587456-10587851	K562	blood:	n/a	n/a
23	MYC	chr2:10587517-10589597	K562	blood:	n/a	chr2:10588126-10588135 chr2:10588941-10588950 chr2:10588939-10588948 chr2:10588651-10588660 chr2:10588126-10588136 chr2:10588125-10588136 chr2:10588939-10588949 chr2:10588496-10588505 chr2:10588124-10588137 chr2:10588938-10588949 chr2:10588125-10588134 chr2:10588938-10588948 chr2:10588125-10588136 chr2:10588938-10588949 chr2:10588930-10588946 chr2:10588939-10588948 chr2:10588500-10588509 chr2:10588125-10588136 chr2:10588124-10588137 chr2:10588939-10588948
24	MAX	chr2:10587485-10589291	MCF-7	breast:	n/a	chr2:10588126-10588135 chr2:10588941-10588950 chr2:10588939-10588948 chr2:10588651-10588660 chr2:10588126-10588136 chr2:10588125-10588136 chr2:10588939-10588949 chr2:10588496-10588505 chr2:10588124-10588137 chr2:10588938-10588949 chr2:10588125-10588134 chr2:10588938-10588948 chr2:10588125-10588136 chr2:10588938-10588949 chr2:10588930-10588946 chr2:10588939-10588948 chr2:10588500-10588509 chr2:10588125-10588136 chr2:10588124-10588137 chr2:10588939-10588948
25	POLR2A	chr2:10586448-10590304	IMR90	lung:	n/a	n/a
26	FOXA1	chr2:10587381-10587955	HepG2	liver:	n/a	n/a
27	POLR2A	chr2:10587492-10589930	K562	blood:	n/a	n/a
28	MAFK	chr2:10587445-10587740	HepG2	liver:	n/a	n/a
29	POLR2A	chr2:10587363-10589635	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr2:10587366-10588600	GM12892	blood:	n/a	n/a
31	POLR2A	chr2:10587476-10590717	Raji	blood:	n/a	n/a
32	POLR2A	chr2:10587376-10588629	Hela-S3	cervix:	n/a	n/a
33	SIN3AK20	chr2:10587481-10589491	PANC-1	pancreas:	n/a	n/a
34	MAZ	chr2:10587505-10589676	IMR90	lung:	n/a	chr2:10588126-10588135 chr2:10588941-10588950 chr2:10588939-10588948 chr2:10588651-10588660 chr2:10588126-10588136 chr2:10588125-10588136 chr2:10588939-10588949 chr2:10588496-10588505 chr2:10588124-10588137 chr2:10588938-10588949 chr2:10588125-10588134 chr2:10588938-10588948 chr2:10588125-10588136 chr2:10588938-10588949 chr2:10588930-10588946 chr2:10588939-10588948 chr2:10588500-10588509 chr2:10588125-10588136 chr2:10588124-10588137 chr2:10588939-10588948
35	MAX	chr2:10587487-10590646	HCT-116	colon:	n/a	chr2:10588126-10588135 chr2:10588941-10588950 chr2:10588939-10588948 chr2:10588651-10588660 chr2:10588126-10588136 chr2:10588125-10588136 chr2:10588939-10588949 chr2:10588496-10588505 chr2:10588124-10588137 chr2:10588938-10588949 chr2:10589691-10589701 chr2:10588125-10588134 chr2:10588938-10588948 chr2:10588125-10588136 chr2:10588938-10588949 chr2:10588930-10588946 chr2:10588939-10588948 chr2:10588500-10588509 chr2:10588125-10588136 chr2:10588124-10588137 chr2:10588939-10588948
36	MYC	chr2:10587524-10589913	K562	blood:	n/a	chr2:10588126-10588135 chr2:10588941-10588950 chr2:10588939-10588948 chr2:10588651-10588660 chr2:10588126-10588136 chr2:10588125-10588136 chr2:10588939-10588949 chr2:10588496-10588505 chr2:10588124-10588137 chr2:10588938-10588949 chr2:10589691-10589701 chr2:10588125-10588134 chr2:10588938-10588948 chr2:10588125-10588136 chr2:10588938-10588949 chr2:10588930-10588946 chr2:10588939-10588948 chr2:10588500-10588509 chr2:10588125-10588136 chr2:10588124-10588137 chr2:10588939-10588948
37	MXI1	chr2:10586728-10589490	K562	blood:	n/a	chr2:10588938-10588947 chr2:10588938-10588947 chr2:10588127-10588136 chr2:10588940-10588949 chr2:10588494-10588509 chr2:10588496-10588511 chr2:10588125-10588134
38	CHD1	chr2:10586355-10588647	IMR90	lung:	n/a	n/a
39	E2F6	chr2:10587444-10589563	A549	lung:	n/a	chr2:10588665-10588674 chr2:10587961-10587970 chr2:10588257-10588267 chr2:10588788-10588797
40	POLR2A	chr2:10587443-10589592	GM12891	blood:	n/a	n/a
41	POLR2A	chr2:10587443-10590033	K562	blood:	n/a	n/a
42	MYBL2	chr2:10587356-10588309	HepG2	liver:	n/a	n/a
43	POLR2A	chr2:10587359-10588628	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr2:10587401-10589642	GM18505	blood:	n/a	n/a
45	HMGN3	chr2:10587511-10589240	K562	blood:	n/a	n/a
46	FOXA1	chr2:10587426-10587925	HepG2	liver:	n/a	n/a
47	FOXA1	chr2:10587384-10587974	HepG2	liver:	n/a	n/a
48	MYC	chr2:10587382-10588946	MCF10A-Er-Src	breast:	n/a	chr2:10588126-10588135 chr2:10588651-10588660 chr2:10588126-10588136 chr2:10588125-10588136 chr2:10588496-10588505 chr2:10588124-10588137 chr2:10588125-10588134 chr2:10588125-10588136 chr2:10588930-10588946 chr2:10588500-10588509 chr2:10588125-10588136 chr2:10588124-10588137
49	MAFF	chr2:10587412-10587797	K562	blood:	n/a	n/a
50	POLR2A	chr2:10587489-10590837	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:10259653..10265917-chr2:10585320..10590295,8	MCF-7	breast:
2	chr2:10586529..10589550-chr2:10592115..10595368,3	MCF-7	breast:
3	chr2:10420712..10423243-chr2:10586890..10589076,2	K562	blood:
4	chr2:10441623..10444200-chr2:10586906..10588748,2	K562	blood:
5	chr2:10441623..10444177-chr2:10587166..10588748,2	K562	blood:
6	chr2:10259839..10264771-chr2:10582056..10590038,19	K562	blood:
7	chr2:10584788..10589777-chr2:10826863..10830293,6	K562	blood:
8	chr2:10259710..10265084-chr2:10586364..10590442,7	MCF-7	breast:
9	chr2:10265245..10266788-chr2:10587089..10589177,2	K562	blood:
10	chr2:10191630..10196148-chr2:10586386..10589794,5	K562	blood:
11	chr2:10257984..10265070-chr2:10582045..10589780,17	K562	blood:
12	chr2:9982517..9985169-chr2:10586715..10588876,2	K562	blood:
13	chr2:10587002..10587961-chr9:130548122..130548787,2	Hela-S3	cervix:

Variant related genes	Relation type
SNORA80B	TF binding region
ENSG00000257135	TF binding region
ENSG00000217258	TF binding region
ENSG00000171848	Chromatin interaction
ENSG00000272524	Chromatin interaction
ENSG00000115756	Chromatin interaction
ENSG00000136807	Chromatin interaction
ENSG00000115761	Chromatin interaction
ENSG00000271787	Chromatin interaction
ENSG00000217258	Chromatin interaction
ENSG00000115750	Chromatin interaction
ENSG00000264030	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530829	chr2:10357105-10655131	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
2	nsv873645	chr2:10537347-10612091	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
3	nsv1007185	chr2:10540386-10791743	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
4	nsv873646	chr2:10550517-10612091	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
5	esv1840383	chr2:10569021-10588903	Active TSS Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
6	nsv873647	chr2:10576424-10597858	Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
7	nsv873648	chr2:10584639-10599493	Active TSS Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
8	esv1819730	chr2:10585164-10591407	Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
9	esv1818042	chr2:10585364-10591407	Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
10	esv1840643	chr2:10585364-10607465	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
11	nsv873649	chr2:10585458-10591628	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
12	nsv873650	chr2:10585458-10597858	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
13	nsv873651	chr2:10585575-10597858	Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
14	esv1792409	chr2:10585687-10588600	Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
15	esv1835530	chr2:10585687-10591407	Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
16	nsv580963	chr2:10586780-10588903	Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
17	esv3388869	chr2:10587326-10589874	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
18	esv3368694	chr2:10587501-10589549	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
19	esv1799664	chr2:10587504-10588903	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
20	esv1802837	chr2:10587504-10588903	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
21	esv1803350	chr2:10587504-10588903	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
22	esv1818199	chr2:10587504-10591407	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10577200-10587800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr2:10584600-10587600	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:10585000-10587600	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:10585000-10587600	Weak transcription	Esophagus	oesophagus
5	chr2:10585000-10587600	Transcr. at gene 5' and 3'	NHEK	skin
6	chr2:10585000-10587800	Weak transcription	Spleen	Spleen
7	chr2:10585200-10587800	Flanking Active TSS	Primary B cells from peripheral blood	blood
8	chr2:10585200-10588000	Flanking Active TSS	Primary B cells from cord blood	blood
9	chr2:10585600-10588000	Active TSS	Fetal Kidney	kidney
10	chr2:10585600-10589000	Active TSS	GM12878-XiMat	blood
11	chr2:10586000-10589600	Active TSS	Pancreatic Islets	Pancreatic Islet
12	chr2:10586200-10587800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr2:10586200-10588200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
14	chr2:10586200-10588800	Active TSS	Fetal Muscle Trunk	muscle
15	chr2:10586200-10589000	Active TSS	HSMM	muscle
16	chr2:10586200-10589000	Active TSS	HSMMtube	muscle
17	chr2:10586200-10589800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr2:10586400-10587600	Flanking Active TSS	Duodenum Mucosa	Duodenum
19	chr2:10586400-10587600	Flanking Active TSS	Dnd41	blood
20	chr2:10586400-10587800	Flanking Active TSS	Fetal Muscle Leg	muscle
21	chr2:10586400-10588800	Active TSS	Colonic Mucosa	Colon
22	chr2:10586400-10589000	Active TSS	Hela-S3	cervix
23	chr2:10586600-10587600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr2:10586600-10587600	Flanking Active TSS	Fetal Stomach	stomach
25	chr2:10586600-10587800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
26	chr2:10586600-10587800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
27	chr2:10586600-10587800	Flanking Active TSS	Fetal Intestine Large	intestine
28	chr2:10586600-10587800	Flanking Active TSS	HUVEC	blood vessel
29	chr2:10586600-10587800	Flanking Active TSS	NH-A	brain
30	chr2:10586600-10587800	Flanking Active TSS	Osteobl	bone
31	chr2:10586600-10588200	Flanking Active TSS	Stomach Smooth Muscle	stomach
32	chr2:10586600-10589000	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr2:10586600-10589000	Active TSS	NHLF	lung
34	chr2:10586600-10589400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr2:10586600-10589400	Active TSS	Psoas Muscle	Psoas
36	chr2:10586600-10589800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr2:10586800-10587600	Flanking Active TSS	NHDF-Ad	bronchial
38	chr2:10586800-10587800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
39	chr2:10586800-10587800	Flanking Active TSS	Liver	Liver
40	chr2:10586800-10587800	Active TSS	Fetal Brain Male	brain
41	chr2:10586800-10587800	Flanking Active TSS	Fetal Thymus	thymus
42	chr2:10586800-10587800	Flanking Active TSS	Thymus	Thymus
43	chr2:10586800-10588000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
44	chr2:10586800-10588000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr2:10586800-10588200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
46	chr2:10586800-10589400	Active TSS	Fetal Brain Female	brain
47	chr2:10586800-10589600	Active TSS	Lung	lung
48	chr2:10587000-10587600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr2:10587000-10587600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr2:10587000-10587600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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