Variant report

Variant	rs2846861
Chromosome Location	chr11:65222305-65222306
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:88)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:88 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POU2F2	chr11:65222280-65223084	GM12878	blood:	n/a	n/a
2	POLR2A	chr11:65222294-65222861	HUVEC	blood vessel:	n/a	n/a
3	RCOR1	chr11:65222289-65223037	K562	blood:	n/a	n/a
4	TCF12	chr11:65222135-65223138	A549	lung:	n/a	n/a
5	POLR2A	chr11:65222303-65223053	MCF-7	breast:	n/a	n/a
6	MAX	chr11:65222252-65222988	K562	blood:	n/a	n/a
7	SMC3	chr11:65222299-65222951	K562	blood:	n/a	n/a
8	RUNX3	chr11:65222277-65223223	GM12878	blood:	n/a	n/a
9	NFATC1	chr11:65222193-65223200	GM12878	blood:	n/a	n/a
10	POLR2A	chr11:65222085-65223002	IMR90	lung:	n/a	n/a
11	POLR2A	chr11:65222231-65222959	HUVEC	blood vessel:	n/a	n/a
12	RCOR1	chr11:65222240-65222980	K562	blood:	n/a	n/a
13	POLR2A	chr11:65222177-65223085	HUVEC	blood vessel:	n/a	n/a
14	STAT5A	chr11:65222241-65223159	GM12878	blood:	n/a	n/a
15	POLR2A	chr11:65222302-65222957	GM15510	blood:	n/a	n/a
16	HEY1	chr11:65222292-65223021	HepG2	liver:	n/a	n/a
17	MTA3	chr11:65221885-65223341	GM12878	blood:	n/a	n/a
18	POLR2A	chr11:65222200-65223194	ProgFib	skin:	n/a	n/a
19	POLR2A	chr11:65222228-65223109	HCT-116	colon:	n/a	n/a
20	POLR2A	chr11:65222228-65223055	GM12891	blood:	n/a	n/a
21	POLR2A	chr11:65222294-65222930	A549	lung:	n/a	n/a
22	SIX5	chr11:65222053-65223026	A549	lung:	n/a	n/a
23	FOXM1	chr11:65222158-65223055	GM12878	blood:	n/a	n/a
24	POLR2A	chr11:65222146-65223109	HepG2	liver:	n/a	n/a
25	POLR2A	chr11:65222179-65223188	K562	blood:	n/a	n/a
26	POLR2A	chr11:65222278-65223111	SK-N-MC	brain:	n/a	n/a
27	POLR2A	chr11:65222281-65223269	GM12892	blood:	n/a	n/a
28	POLR2A	chr11:65221313-65224497	U87	brain:	n/a	n/a
29	GABPA	chr11:65222284-65222797	K562	blood:	n/a	chr11:65222641-65222650
30	POLR2A	chr11:65221907-65223320	PANC-1	pancreas:	n/a	n/a
31	POLR2A	chr11:65222265-65223173	K562	blood:	n/a	n/a
32	POLR2A	chr11:65222250-65222946	ECC-1	luminal epithelium:	n/a	n/a
33	CBX3	chr11:65222250-65223052	K562	blood:	n/a	n/a
34	THAP1	chr11:65222205-65222453	K562	blood:	n/a	n/a
35	ELF1	chr11:65222169-65223130	GM12878	blood:	n/a	n/a
36	CHD1	chr11:65221247-65223345	IMR90	lung:	n/a	n/a
37	POLR2A	chr11:65221644-65223363	U87	brain:	n/a	n/a
38	POLR2A	chr11:65222192-65223179	GM12878	blood:	n/a	n/a
39	RAD21	chr11:65222124-65222825	IMR90	lung:	n/a	n/a
40	ZBTB7A	chr11:65222186-65222815	ECC-1	luminal epithelium:	n/a	chr11:65222607-65222616
41	POLR2A	chr11:65222197-65223159	GM12878	blood:	n/a	n/a
42	SIN3AK20	chr11:65222081-65223183	MCF-7	breast:	n/a	n/a
43	POLR2A	chr11:65222206-65223328	GM12892	blood:	n/a	n/a
44	POLR2A	chr11:65222249-65223035	HUVEC	blood vessel:	n/a	n/a
45	POLR2A	chr11:65222281-65223005	ECC-1	luminal epithelium:	n/a	n/a
46	STAT5A	chr11:65222104-65223227	GM12878	blood:	n/a	n/a
47	JUN	chr11:65221883-65223238	K562	blood:	n/a	n/a
48	SP1	chr11:65222271-65222952	A549	lung:	n/a	n/a
49	POLR2A	chr11:65222271-65223041	MCF-7	breast:	n/a	n/a
50	CTCF	chr11:65222180-65222330	GM12871	blood:	n/a	n/a

No data

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:65122004..65123879-chr11:65220475..65223059,2	K562	blood:
2	chr11:62608095..62609669-chr11:65220631..65223111,2	MCF-7	breast:
3	chr11:65178877..65218546-chr11:65218612..65286191,1014	K562	blood:

No data

Variant related genes	Relation type
ENSG00000173727	TF binding region
ENSG00000245532	Chromatin interaction
ENSG00000173825	Chromatin interaction
ENSG00000133316	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10896001	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11227204	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1152619	0.86[JPT][hapmap]
rs11822111	0.84[AMR][1000 genomes]
rs1616810	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1621277	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1626021	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1784100	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1784101	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1784858	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1784859	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1784860	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2105608	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2508711	0.86[ASN][1000 genomes]
rs2508712	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2957268	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2957269	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3015965	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3015966	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3016343	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3132743	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3132767	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs512715	0.83[MEX][hapmap]
rs587080	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs587390	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs588298	0.96[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs600231	0.82[JPT][hapmap];0.82[MEX][hapmap]
rs602838	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs604676	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs605035	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs660588	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs661403	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs674485	0.83[MEX][hapmap]
rs682845	0.96[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs694243	0.83[MEX][hapmap]
rs7114809	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7934628	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526181	chr11:64638041-65257329	Flanking Active TSS Enhancers Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1539 gene(s)	inside rSNPs	diseases
2	esv2422285	chr11:65013294-65254540	Genic enhancers Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	474 gene(s)	inside rSNPs	diseases
3	nsv897715	chr11:65083491-65427346	Enhancers Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	984 gene(s)	inside rSNPs	diseases
4	nsv897716	chr11:65083491-65481166	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	999 gene(s)	inside rSNPs	diseases
5	nsv541065	chr11:65117387-65271894	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	835 gene(s)	inside rSNPs	diseases
6	esv1829999	chr11:65136686-65343124	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	963 gene(s)	inside rSNPs	diseases
7	nsv897717	chr11:65140209-65278461	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	942 gene(s)	inside rSNPs	diseases
8	nsv897718	chr11:65140209-65577516	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1003 gene(s)	inside rSNPs	diseases
9	nsv541066	chr11:65142779-65271894	Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	833 gene(s)	inside rSNPs	diseases
10	nsv541067	chr11:65142779-65313799	Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	950 gene(s)	inside rSNPs	diseases
11	nsv541068	chr11:65142779-65331136	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	953 gene(s)	inside rSNPs	diseases
12	nsv541069	chr11:65142779-65368787	Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	965 gene(s)	inside rSNPs	diseases
13	nsv541070	chr11:65142779-65397058	Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	972 gene(s)	inside rSNPs	diseases
14	nsv541071	chr11:65142779-65429352	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	984 gene(s)	inside rSNPs	diseases
15	nsv897719	chr11:65157094-65335705	Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	949 gene(s)	inside rSNPs	diseases
16	nsv541072	chr11:65171202-65313799	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	946 gene(s)	inside rSNPs	diseases
17	nsv541073	chr11:65171202-65331136	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	949 gene(s)	inside rSNPs	diseases
18	nsv541074	chr11:65171202-65368787	Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	961 gene(s)	inside rSNPs	diseases
19	nsv541075	chr11:65210592-65331136	Genic enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	620 gene(s)	inside rSNPs	diseases
20	nsv541076	chr11:65210592-65397058	Flanking Active TSS Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	645 gene(s)	inside rSNPs	diseases
21	nsv897720	chr11:65213434-65445950	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	665 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs2846861	VWCE	cis	parietal	SCAN
rs2846861	BBS1	cis	parietal	SCAN
rs2846861	NEAT1	cis	Adipose Subcutaneous	GTEx
rs2846861	NEAT1	cis	Nerve Tibial	GTEx
rs2846861	C11orf83	cis	parietal	SCAN
rs2846861	SCGB2A2	cis	parietal	SCAN
rs2846861	TncRNA	Cis_1M	lymphoblastoid	RTeQTL
rs2846861	NEAT1	cis	Esophagus Mucosa	GTEx
rs2846861	STX5	cis	parietal	SCAN
rs2846861	NEAT1	cis	Muscle Skeletal	GTEx

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65212800-65222400	Weak transcription	Stomach Mucosa	stomach
2	chr11:65220400-65227000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:65221400-65222400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr11:65221600-65222400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr11:65221600-65222800	Active TSS	H9 Cell Line	embryonic stem cell
6	chr11:65221600-65222800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:65221800-65222400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr11:65221800-65222400	Flanking Active TSS	HepG2	liver
9	chr11:65221800-65222600	Enhancers	Spleen	Spleen
10	chr11:65221800-65222800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr11:65221800-65222800	Active TSS	Colonic Mucosa	Colon
12	chr11:65221800-65222800	Active TSS	Rectal Smooth Muscle	rectum
13	chr11:65221800-65222800	Flanking Active TSS	Osteobl	bone
14	chr11:65221800-65223200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr11:65221800-65223200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr11:65221800-65223200	Flanking Active TSS	Stomach Smooth Muscle	stomach
17	chr11:65221800-65223200	Flanking Active TSS	HSMM	muscle
18	chr11:65221800-65223200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr11:65221800-65225400	Active TSS	GM12878-XiMat	blood
20	chr11:65222000-65222400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
21	chr11:65222000-65222400	Flanking Active TSS	Primary T cells from cord blood	blood
22	chr11:65222000-65222400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
23	chr11:65222000-65222400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
24	chr11:65222000-65222400	Active TSS	Brain Anterior Caudate	brain
25	chr11:65222000-65222400	Enhancers	Fetal Brain Male	brain
26	chr11:65222000-65222400	Flanking Active TSS	Fetal Intestine Large	intestine
27	chr11:65222000-65222400	Flanking Active TSS	Fetal Intestine Small	intestine
28	chr11:65222000-65222400	Flanking Active TSS	Fetal Lung	lung
29	chr11:65222000-65222400	Flanking Active TSS	Fetal Stomach	stomach
30	chr11:65222000-65222400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
31	chr11:65222000-65222400	Flanking Active TSS	Thymus	Thymus
32	chr11:65222000-65222400	Flanking Active TSS	HSMMtube	muscle
33	chr11:65222000-65222400	Flanking Active TSS	K562	blood
34	chr11:65222000-65222800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
35	chr11:65222000-65222800	Active TSS	Aorta	Aorta
36	chr11:65222000-65222800	Active TSS	Brain Hippocampus Middle	brain
37	chr11:65222000-65222800	Active TSS	Brain Inferior Temporal Lobe	brain
38	chr11:65222000-65222800	Active TSS	Duodenum Smooth Muscle	Duodenum
39	chr11:65222000-65222800	Active TSS	Psoas Muscle	Psoas
40	chr11:65222000-65222800	Active TSS	A549	lung
41	chr11:65222000-65223000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
42	chr11:65222000-65223000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
43	chr11:65222000-65223000	Flanking Active TSS	Primary hematopoietic stem cells	blood
44	chr11:65222000-65223000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
45	chr11:65222000-65223000	Active TSS	Brain Germinal Matrix	brain
46	chr11:65222000-65223000	Flanking Active TSS	HUVEC	blood vessel
47	chr11:65222000-65223000	Flanking Active TSS	NHEK	skin
48	chr11:65222000-65223200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr11:65222000-65223200	Flanking Active TSS	Primary B cells from cord blood	blood
50	chr11:65222000-65223200	Flanking Active TSS	Primary B cells from peripheral blood	blood

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