Variant report

Variant	rs12362915
Chromosome Location	chr11:63974154-63974155
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:169)
CpG islands
(count:183)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:169 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:63973771-63976077	U87	brain:	n/a	n/a
2	POLR2A	chr11:63972847-63976061	GM12891	blood:	n/a	n/a
3	TBP	chr11:63973889-63975530	K562	blood:	n/a	n/a
4	PML	chr11:63973759-63974439	K562	blood:	n/a	n/a
5	GABPA	chr11:63973757-63974529	K562	blood:	n/a	n/a
6	POLR2A	chr11:63973087-63975757	GM12878	blood:	n/a	n/a
7	POU2F2	chr11:63974077-63975564	GM12891	blood:	n/a	n/a
8	PML	chr11:63973613-63975622	K562	blood:	n/a	chr11:63975049-63975057 chr11:63975106-63975115
9	MYC	chr11:63973624-63975764	K562	blood:	n/a	chr11:63973884-63973893 chr11:63973992-63974002
10	CCNT2	chr11:63973900-63975557	K562	blood:	n/a	chr11:63974266-63974275 chr11:63975509-63975518
11	POLR2A	chr11:63972904-63976551	GM12878	blood:	n/a	n/a
12	IRF1	chr11:63974014-63974416	K562	blood:	n/a	chr11:63974319-63974328
13	POLR2A	chr11:63973231-63976656	GM12878	blood:	n/a	n/a
14	NR2F2	chr11:63973768-63975984	K562	blood:	n/a	n/a
15	MAX	chr11:63973836-63974489	K562	blood:	n/a	chr11:63973884-63973893 chr11:63973992-63974002
16	POLR2A	chr11:63972968-63979020	GM12878	blood:	n/a	n/a
17	POLR2A	chr11:63973082-63976238	K562	blood:	n/a	n/a
18	POLR2A	chr11:63972926-63975688	HL-60	blood:	n/a	n/a
19	ELF1	chr11:63972952-63975775	GM12878	blood:	n/a	chr11:63973154-63973165 chr11:63975062-63975071 chr11:63975061-63975072 chr11:63973114-63973127
20	ATF2	chr11:63973260-63974846	GM12878	blood:	n/a	n/a
21	EP300	chr11:63973814-63974238	GM12878	blood:	n/a	chr11:63974113-63974129
22	POLR2A	chr11:63972869-63978649	K562	blood:	n/a	n/a
23	PAX5	chr11:63973738-63975649	GM12878	blood:	n/a	n/a
24	RELA	chr11:63973037-63974516	GM18951	blood:	n/a	n/a
25	RCOR1	chr11:63973840-63975581	K562	blood:	n/a	n/a
26	POLR2A	chr11:63972859-63975682	PFSK-1	brain:	n/a	n/a
27	SPI1	chr11:63973680-63974353	HL-60	blood:	n/a	n/a
28	BHLHE40	chr11:63973937-63975538	K562	blood:	n/a	chr11:63974489-63974505
29	STAT5A	chr11:63972958-63975971	GM12878	blood:	n/a	chr11:63974138-63974150 chr11:63973245-63973256 chr11:63973221-63973228
30	POLR2A	chr11:63973192-63976000	HUVEC	blood vessel:	n/a	n/a
31	MYC	chr11:63973745-63975597	NB4	blood:	n/a	chr11:63973884-63973893 chr11:63973992-63974002
32	TAF1	chr11:63973802-63974411	K562	blood:	n/a	n/a
33	POLR2A	chr11:63972913-63974731	PANC-1	pancreas:	n/a	n/a
34	EBF1	chr11:63973775-63975565	GM12878	blood:	n/a	chr11:63974054-63974063 chr11:63974054-63974064 chr11:63974390-63974399 chr11:63974053-63974064
35	MYC	chr11:63973905-63975590	K562	blood:	n/a	chr11:63973992-63974002
36	POLR2A	chr11:63972929-63976250	GM12892	blood:	n/a	n/a
37	HEY1	chr11:63973201-63977331	K562	blood:	n/a	chr11:63975289-63975298
38	MAX	chr11:63973720-63975880	K562	blood:	n/a	chr11:63973884-63973893 chr11:63973992-63974002
39	JUND	chr11:63973773-63974476	K562	blood:	n/a	n/a
40	NFIC	chr11:63973541-63974470	GM12878	blood:	n/a	n/a
41	RCOR1	chr11:63974081-63975583	K562	blood:	n/a	n/a
42	POLR2A	chr11:63972963-63975964	SK-N-MC	brain:	n/a	n/a
43	CHD2	chr11:63973077-63975776	K562	blood:	n/a	n/a
44	HEY1	chr11:63973758-63975657	K562	blood:	n/a	chr11:63975289-63975298
45	STAT5A	chr11:63973894-63974239	GM12878	blood:	n/a	chr11:63974138-63974150
46	POLR2A	chr11:63973058-63976444	GM12892	blood:	n/a	n/a
47	MXI1	chr11:63974025-63974331	K562	blood:	n/a	n/a
48	POLR2A	chr11:63972937-63980346	K562	blood:	n/a	n/a
49	EP300	chr11:63973795-63974397	K562	blood:	n/a	chr11:63974113-63974129
50	POLR2A	chr11:63971678-63979009	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:63974153-63974203	AoSMC	blood vessel:	n/a
2	chr11:63974123-63974173	GM12891	blood:	n/a
3	chr11:63974123-63974173	HL-60	blood:	n/a
4	chr11:63974123-63974173	Hepatocyte	liver:	n/a
5	chr11:63974131-63974181	NHBE	bronchial:	n/a
6	chr11:63974153-63974203	HIPEpiC	eye:	n/a
7	chr11:63974123-63974173	HCT-116	colon:	n/a
8	chr11:63974123-63974173	SKMC	muscle:	n/a
9	chr11:63974153-63974203	GM12891	blood:	n/a
10	chr11:63974131-63974181	PFSK-1	brain:	n/a
11	chr11:63974131-63974181	SK-N-SH_RA	brain:	n/a
12	chr11:63974123-63974173	U87	brain:	n/a
13	chr11:63974153-63974203	PFSK-1	brain:	n/a
14	chr11:63974123-63974173	MCF10A-Er-Src	breast:	n/a
15	chr11:63974131-63974181	HAEpiC	amniotic membrane:	n/a
16	chr11:63974123-63974173	T-47D	breast:	n/a
17	chr11:63974153-63974203	GM12878	blood:	n/a
18	chr11:63974153-63974203	HCF	heart:	n/a
19	chr11:63974153-63974203	LNCaP	prostate:	n/a
20	chr11:63974153-63974203	HPAEpiC	pulmonary alveolar:	n/a
21	chr11:63974123-63974173	GM06990	blood:	n/a
22	chr11:63974153-63974203	Caco-2	colon:	n/a
23	chr11:63974131-63974181	HMEC	breast:	n/a
24	chr11:63974153-63974203	HUVEC	blood vessel:	n/a
25	chr11:63974131-63974181	HRCEpiC	kidney:	n/a
26	chr11:63974153-63974203	NB4	blood:	n/a
27	chr11:63974153-63974203	MCF10A-Er-Src	breast:	n/a
28	chr11:63974123-63974173	NHBE	bronchial:	n/a
29	chr11:63974153-63974203	HRPEpiC	eye:	n/a
30	chr11:63974131-63974181	LNCaP	prostate:	n/a
31	chr11:63974153-63974203	GM06990	blood:	n/a
32	chr11:63974131-63974181	PANC-1	pancreas:	n/a
33	chr11:63974131-63974181	SKMC	muscle:	n/a
34	chr11:63974123-63974173	HRE	kidney:	n/a
35	chr11:63974131-63974181	AG09309	skin:	n/a
36	chr11:63974123-63974173	HAEpiC	amniotic membrane:	n/a
37	chr11:63974153-63974203	NHDF-neo	bronchial:	n/a
38	chr11:63974131-63974181	ECC-1	luminal epithelium:	n/a
39	chr11:63974123-63974173	BE2_C	brain:	n/a
40	chr11:63974131-63974181	HIPEpiC	eye:	n/a
41	chr11:63974123-63974173	HMEC	breast:	n/a
42	chr11:63974123-63974173	ECC-1	luminal epithelium:	n/a
43	chr11:63974153-63974203	CMK	blood:	n/a
44	chr11:63974153-63974203	SK-N-SH_RA	brain:	n/a
45	chr11:63974153-63974203	SK-N-SH	brain:	n/a
46	chr11:63974131-63974181	Hela-S3	cervix:	n/a
47	chr11:63974123-63974173	MCF-7	breast:	n/a
48	chr11:63974123-63974173	ProgFib	skin:	n/a
49	chr11:63974131-63974181	K562	blood:	n/a
50	chr11:63974153-63974203	RPTEC	kidney:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:63972047..63977847-chr11:64122012..64128099,8	K562	blood:
2	chr11:63969363..63977705-chr11:64080619..64088284,16	K562	blood:
3	chr11:63972230..63976425-chr11:64106710..64112651,7	K562	blood:
4	chr11:63951359..63955952-chr11:63973161..63976481,4	MCF-7	breast:
5	chr11:63973802..63976476-chr11:64070377..64073257,2	MCF-7	breast:
6	chr11:62607620..62609636-chr11:63971953..63974699,2	MCF-7	breast:
7	chr11:63740485..63742258-chr11:63973387..63975999,2	K562	blood:
8	chr1:17231194..17231908-chr11:63973619..63974205,2	NB4	blood:
9	chr11:63973628..63976272-chr11:64056827..64059574,2	MCF-7	breast:
10	chr11:63973691..63975490-chr11:64083933..64085958,2	MCF-7	breast:
11	chr11:63932241..63934493-chr11:63974004..63976708,3	K562	blood:
12	chr11:63930981..63933673-chr11:63971506..63975446,4	K562	blood:
13	chr11:63972384..63977847-chr11:64121311..64126015,8	K562	blood:

No data

Variant related genes	Relation type
FERMT3	TF binding region
FERMT3	CpG island
ENSG00000182450	Chromatin interaction
ENSG00000257069	Chromatin interaction
ENSG00000173113	Chromatin interaction
ENSG00000256100	Chromatin interaction
ENSG00000133315	Chromatin interaction
ENSG00000126432	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000176340	Chromatin interaction
ENSG00000173153	Chromatin interaction
ENSG00000162302	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000168071	Chromatin interaction
ENSG00000168439	Chromatin interaction
ENSG00000272426	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs14788	1.00[LWK][hapmap]
rs2232407	1.00[LWK][hapmap]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	254 gene(s)	inside rSNPs	diseases
2	esv1802079	chr11:63746066-64151373	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	247 gene(s)	inside rSNPs	diseases
3	nsv897646	chr11:63754986-64150370	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
4	nsv1035875	chr11:63800238-64132030	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	234 gene(s)	inside rSNPs	diseases
5	nsv469961	chr11:63822940-64085967	Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
6	nsv897660	chr11:63860826-64125142	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription 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	231 gene(s)	inside rSNPs	diseases
7	nsv897661	chr11:63863405-64129722	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
8	nsv897662	chr11:63889749-64150370	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
9	nsv897664	chr11:63919742-64150370	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
10	nsv468592	chr11:63924446-64042997	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	166 gene(s)	inside rSNPs	diseases
11	nsv555184	chr11:63924446-64042997	Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	166 gene(s)	inside rSNPs	diseases
12	nsv897665	chr11:63927695-64026144	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	155 gene(s)	inside rSNPs	diseases
13	nsv897666	chr11:63929493-64026144	Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	155 gene(s)	inside rSNPs	diseases
14	nsv869944	chr11:63932152-64123062	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	227 gene(s)	inside rSNPs	diseases
15	nsv468593	chr11:63941734-64089874	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
16	nsv555185	chr11:63941734-64089874	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer 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 target site	212 gene(s)	inside rSNPs	diseases
17	nsv555186	chr11:63949095-64097233	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
18	nsv468595	chr11:63953121-64027888	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription 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	146 gene(s)	inside rSNPs	diseases
19	nsv555187	chr11:63953121-64027888	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	146 gene(s)	inside rSNPs	diseases
20	nsv897667	chr11:63964657-64078380	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	141 gene(s)	inside rSNPs	diseases
21	nsv897668	chr11:63964657-64085298	Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	163 gene(s)	inside rSNPs	diseases
22	nsv897669	chr11:63964657-64089874	Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
23	nsv897670	chr11:63964657-64097233	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
24	nsv897671	chr11:63964657-64150370	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer 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	179 gene(s)	inside rSNPs	diseases
25	nsv541061	chr11:63970174-64010995	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	76 gene(s)	inside rSNPs	diseases
26	nsv832186	chr11:63972260-64170059	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	180 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63955200-63974400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:63955200-63975000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
3	chr11:63955200-63975200	Strong transcription	HUES64 Cell Line	embryonic stem cell
4	chr11:63955800-63975400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:63956200-63974200	Weak transcription	Right Atrium	heart
6	chr11:63957400-63974800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr11:63957400-63975800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr11:63959600-63975000	Strong transcription	NHEK	skin
9	chr11:63959600-63976000	Strong transcription	Fetal Brain Female	brain
10	chr11:63959600-63977000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
11	chr11:63959800-63976000	Strong transcription	HUES48 Cell Line	embryonic stem cell
12	chr11:63960000-63974400	Strong transcription	Brain Substantia Nigra	brain
13	chr11:63960000-63975400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
14	chr11:63960000-63975600	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:63960000-63976200	Strong transcription	H1 Cell Line	embryonic stem cell
16	chr11:63964000-63975200	Strong transcription	Brain Angular Gyrus	brain
17	chr11:63964400-63974400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr11:63967200-63975600	Strong transcription	Placenta Amnion	Placenta Amnion
19	chr11:63967400-63976200	Strong transcription	Brain Germinal Matrix	brain
20	chr11:63968000-63974400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr11:63969400-63974200	Genic enhancers	Skeletal Muscle Male	skeletal muscle
22	chr11:63970200-63979000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr11:63970600-63975200	Weak transcription	Fetal Brain Male	brain
24	chr11:63971000-63974200	Weak transcription	Small Intestine	intestine
25	chr11:63971200-63974200	Genic enhancers	Fetal Muscle Leg	muscle
26	chr11:63971400-63974200	Genic enhancers	Fetal Muscle Trunk	muscle
27	chr11:63971600-63992800	Weak transcription	Fetal Kidney	kidney
28	chr11:63972000-63974200	Weak transcription	Psoas Muscle	Psoas
29	chr11:63972000-63974800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr11:63972000-63980000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr11:63972000-63990000	Weak transcription	Ovary	ovary
32	chr11:63972200-63974200	Weak transcription	Lung	lung
33	chr11:63972200-63974200	Strong transcription	HMEC	breast
34	chr11:63972200-63975000	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr11:63972400-63974200	Strong transcription	Brain Cingulate Gyrus	brain
36	chr11:63972400-63974200	Strong transcription	Brain Hippocampus Middle	brain
37	chr11:63972400-63974200	Strong transcription	Brain Inferior Temporal Lobe	brain
38	chr11:63972400-63974200	Weak transcription	Colon Smooth Muscle	Colon
39	chr11:63972400-63974200	Weak transcription	NHDF-Ad	bronchial
40	chr11:63972400-63974400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr11:63972400-63974400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr11:63972400-63974400	Weak transcription	Fetal Lung	lung
43	chr11:63972400-63974400	Weak transcription	NH-A	brain
44	chr11:63972400-63974400	Strong transcription	Osteobl	bone
45	chr11:63972400-63975400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr11:63972400-63976200	Strong transcription	A549	lung
47	chr11:63972600-63974200	Strong transcription	Cortex derived primary cultured neurospheres	brain
48	chr11:63972600-63974200	Strong transcription	Brain Anterior Caudate	brain
49	chr11:63972600-63974200	Strong transcription	Fetal Stomach	stomach
50	chr11:63972600-63974800	Weak transcription	Pancreatic Islets	Pancreatic Islet

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