Variant report

Variant	rs4102217
Chromosome Location	chr11:65263895-65263896
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	chr11:65263137-65276123	GM12878	blood:	n/a	n/a
2	NR2F2	chr11:65263528-65265745	K562	blood:	n/a	n/a
3	POLR2A	chr11:65263707-65276561	K562	blood:	n/a	n/a
4	POLR2A	chr11:65263591-65276127	GM12878	blood:	n/a	n/a
5	HEY1	chr11:65263782-65276303	K562	blood:	n/a	chr11:65265117-65265132 chr11:65265814-65265829
6	POLR2A	chr11:65263742-65264033	SK-N-SH	brain:	n/a	n/a
7	ZNF384	chr11:65263617-65263897	K562	blood:	n/a	n/a
8	TAF1	chr11:65263639-65264153	PFSK-1	brain:	n/a	n/a
9	GATA3	chr11:65263720-65264419	SH-SY5Y	brain:	n/a	chr11:65264284-65264294
10	POLR2A	chr11:65263586-65276720	PANC-1	pancreas:	n/a	n/a
11	REST	chr11:65263736-65264066	PFSK-1	brain:	n/a	n/a
12	POLR2A	chr11:65263679-65275464	H1-neurons	neurons:	n/a	n/a
13	TCF12	chr11:65263687-65264577	SK-N-SH	brain:	n/a	n/a
14	EP300	chr11:65263711-65267410	K562	blood:	n/a	chr11:65264255-65264268 chr11:65265612-65265622 chr11:65264162-65264176 chr11:65264157-65264171 chr11:65265120-65265136 chr11:65264167-65264181
15	POLR2A	chr11:65263184-65276060	GM12892	blood:	n/a	n/a
16	TEAD4	chr11:65263655-65275540	K562	blood:	n/a	chr11:65272376-65272385
17	ESR1	chr11:65263797-65264236	T-47D	breast:	n/a	n/a
18	POLR2A	chr11:65263623-65276062	GM12892	blood:	n/a	n/a
19	POLR2A	chr11:65263590-65264013	H1-neurons	neurons:	n/a	n/a
20	MXI1	chr11:65263495-65275543	SK-N-SH	brain:	n/a	chr11:65264243-65264252
21	POLR2A	chr11:65263703-65276201	K562	blood:	n/a	n/a
22	TCF12	chr11:65263561-65265600	SK-N-SH	brain:	n/a	chr11:65264911-65264918
23	EP300	chr11:65263565-65264330	SK-N-SH_RA	brain:	n/a	chr11:65264255-65264268 chr11:65264162-65264176 chr11:65264157-65264171 chr11:65264167-65264181
24	POLR2A	chr11:65263681-65264063	K562	blood:	n/a	n/a
25	TCF12	chr11:65263778-65276589	A549	lung:	n/a	chr11:65271318-65271326 chr11:65264911-65264918
26	POLR2A	chr11:65263700-65276346	HUVEC	blood vessel:	n/a	n/a
27	SIN3AK20	chr11:65263832-65267191	MCF-7	breast:	n/a	n/a
28	GATA3	chr11:65263762-65264162	T-47D	breast:	n/a	n/a
29	WRNIP1	chr11:65263844-65266669	GM12878	blood:	n/a	n/a
30	YY1	chr11:65263760-65264148	SK-N-SH_RA	brain:	n/a	n/a
31	ESR1	chr11:65263782-65264214	T-47D	breast:	n/a	n/a
32	ESR1	chr11:65263781-65264166	T-47D	breast:	n/a	n/a
33	POLR2A	chr11:65263584-65276225	PFSK-1	brain:	n/a	n/a
34	EP300	chr11:65263486-65267167	SK-N-SH	brain:	n/a	chr11:65264255-65264268 chr11:65265612-65265622 chr11:65264162-65264176 chr11:65264157-65264171 chr11:65265120-65265136 chr11:65264167-65264181
35	GATA2	chr11:65263765-65265422	SH-SY5Y	brain:	n/a	chr11:65264772-65264782 chr11:65264284-65264294
36	REST	chr11:65263786-65264009	K562	blood:	n/a	n/a
37	RCOR1	chr11:65263760-65264114	K562	blood:	n/a	n/a
38	IRF1	chr11:65263681-65272365	K562	blood:	n/a	chr11:65266380-65266397 chr11:65264580-65264594 chr11:65264582-65264593 chr11:65264818-65264832 chr11:65264578-65264592 chr11:65268590-65268600 chr11:65266380-65266392 chr11:65268723-65268737 chr11:65266380-65266392 chr11:65265506-65265520 chr11:65264582-65264596 chr11:65266381-65266392 chr11:65264918-65264932 chr11:65264582-65264595 chr11:65265184-65265198 chr11:65268381-65268395 chr11:65264581-65264595 chr11:65268383-65268393 chr11:65265505-65265517 chr11:65268379-65268393 chr11:65271754-65271768 chr11:65269013-65269022
39	MAZ	chr11:65263840-65264484	K562	blood:	n/a	n/a
40	POLR2A	chr11:65263641-65276461	U87	brain:	n/a	n/a
41	REST	chr11:65263785-65264089	SK-N-SH	brain:	n/a	n/a
42	ESR1	chr11:65263789-65264140	T-47D	breast:	n/a	n/a
43	RAD21	chr11:65263690-65264143	SK-N-SH_RA	brain:	n/a	n/a
44	POLR2A	chr11:65263642-65276479	SK-N-SH	brain:	n/a	n/a
45	EP300	chr11:65263574-65264158	SK-N-SH_RA	brain:	n/a	n/a
46	JUND	chr11:65263824-65263962	K562	blood:	n/a	n/a
47	POLR2A	chr11:65263725-65276261	SK-N-MC	brain:	n/a	n/a
48	TBL1XR1	chr11:65263808-65275424	K562	blood:	n/a	n/a
49	EP300	chr11:65263796-65264469	T-47D	breast:	n/a	chr11:65264255-65264268 chr11:65264162-65264176 chr11:65264157-65264171 chr11:65264167-65264181
50	MTA3	chr11:65263609-65276355	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:65263786..65274103-chr11:65335962..65346813,28	MCF-7	breast:
2	chr11:64845733..64847412-chr11:65262539..65264597,2	K562	blood:
3	chr11:65178877..65218546-chr11:65218612..65286191,1014	K562	blood:
4	chr11:65263752..65266788-chr11:65624237..65626722,4	K562	blood:
5	chr11:65262963..65264911-chr11:65321406..65323614,2	K562	blood:
6	chr11:65263708..65266379-chr11:65359213..65361243,2	K562	blood:
7	chr11:65263261..65267812-chr11:65306192..65309215,4	MCF-7	breast:
8	chr11:65263855..65269766-chr11:65381384..65386650,8	MCF-7	breast:
9	chr11:65263558..65266439-chr11:65666909..65668740,3	K562	blood:
10	chr11:65116402..65157784-chr11:65261420..65278410,154	K562	blood:
11	chr11:65263752..65266249-chr11:65624237..65626407,2	K562	blood:
12	chr11:65262109..65269742-chr11:65336183..65344125,16	MCF-7	breast:
13	chr11:65261343..65264179-chr11:65354610..65357170,2	K562	blood:
14	chr11:65262833..65264423-chr11:65305627..65307751,2	K562	blood:
15	chr11:65263724..65269268-chr11:65338505..65344270,10	K562	blood:
16	chr11:65262283..65263978-chr11:65419665..65421629,2	K562	blood:

Variant related genes	Relation type
MALAT1	TF binding region
ENSG00000197136	Chromatin interaction
ENSG00000175592	Chromatin interaction
ENSG00000173442	Chromatin interaction
ENSG00000245532	Chromatin interaction
ENSG00000172732	Chromatin interaction
ENSG00000173338	Chromatin interaction
ENSG00000172757	Chromatin interaction
ENSG00000269018	Chromatin interaction
ENSG00000162241	Chromatin interaction
ENSG00000146670	Chromatin interaction
ENSG00000173465	Chromatin interaction
ENSG00000168056	Chromatin interaction
ENSG00000173825	Chromatin interaction
ENSG00000126391	Chromatin interaction
ENSG00000173327	Chromatin interaction
ENSG00000255478	Chromatin interaction
ENSG00000260233	Chromatin interaction
ENSG00000176973	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10896004	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10896005	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10896006	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10896007	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs10896008	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10896009	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10896010	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10896012	0.91[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11227196	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11227197	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11227198	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11227199	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11227200	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11227201	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11227202	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11227205	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11227206	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12269965	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12269975	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12294910	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12360896	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12364730	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12788055	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12808303	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17146964	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2508710	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34527830	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34582634	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34877911	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35292734	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35469818	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35826299	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57311037	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7128776	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7931615	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7935551	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65252800-65264400	Enhancers	Placenta	Placenta
2	chr11:65252800-65265200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr11:65253200-65264000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr11:65253400-65264400	Enhancers	Left Ventricle	heart
5	chr11:65254200-65264200	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr11:65254800-65264200	Enhancers	Primary B cells from peripheral blood	blood
7	chr11:65255800-65264200	Enhancers	Fetal Stomach	stomach
8	chr11:65255800-65264200	Enhancers	Stomach Mucosa	stomach
9	chr11:65256000-65264000	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr11:65256000-65264000	Enhancers	Fetal Muscle Trunk	muscle
11	chr11:65256000-65264000	Enhancers	Fetal Muscle Leg	muscle
12	chr11:65256000-65265200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr11:65256200-65265200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr11:65258800-65264200	Enhancers	Primary hematopoietic stem cells	blood
15	chr11:65259800-65264000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr11:65259800-65264000	Enhancers	Fetal Heart	heart
17	chr11:65260400-65264000	Enhancers	Primary B cells from cord blood	blood
18	chr11:65260600-65264200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr11:65261000-65264000	Enhancers	Brain Anterior Caudate	brain
20	chr11:65261000-65265200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr11:65261000-65265200	Weak transcription	Gastric	stomach
22	chr11:65261200-65264200	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr11:65261800-65264200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr11:65261800-65264200	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr11:65261800-65265200	Weak transcription	Ovary	ovary
26	chr11:65262000-65264200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr11:65262400-65264000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr11:65262400-65264200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr11:65262800-65264000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr11:65263000-65264000	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr11:65263000-65264000	Enhancers	Fetal Lung	lung
32	chr11:65263000-65264200	Enhancers	NH-A	brain
33	chr11:65263200-65264000	Enhancers	Fetal Kidney	kidney
34	chr11:65263200-65264000	Enhancers	Psoas Muscle	Psoas
35	chr11:65263200-65264200	Enhancers	Primary T cells fromperipheralblood	blood
36	chr11:65263200-65264200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr11:65263200-65264800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr11:65263200-65265000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr11:65263200-65265000	Enhancers	Placenta Amnion	Placenta Amnion
40	chr11:65263400-65264000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr11:65263400-65264000	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr11:65263400-65264200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr11:65263400-65264200	Enhancers	Primary T helper cells fromperipheralblood	blood
44	chr11:65263400-65264200	Enhancers	Brain Substantia Nigra	brain
45	chr11:65263400-65264400	Enhancers	Fetal Intestine Large	intestine
46	chr11:65263400-65264400	Enhancers	HMEC	breast
47	chr11:65263400-65264600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr11:65263400-65264600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr11:65263400-65264600	Enhancers	Lung	lung
50	chr11:65263400-65264800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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