Variant report

Variant	rs12286110
Chromosome Location	chr11:67788035-67788036
allele	A/C
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	chr11:67788001-67788239	A549	lung:	n/a	n/a
2	CTCF	chr11:67787305-67789655	A549	lung:	n/a	chr11:67788221-67788234 chr11:67788247-67788268 chr11:67788245-67788263 chr11:67788383-67788392 chr11:67788246-67788262
3	RAD21	chr11:67788010-67788512	H1-hESC	embryonic stem cell:	n/a	chr11:67788491-67788501 chr11:67788246-67788265
4	MAX	chr11:67787401-67789169	A549	lung:	n/a	chr11:67788672-67788682
5	MYC	chr11:67788012-67788328	MCF10A-Er-Src	breast:	n/a	n/a
6	POLR2A	chr11:67787952-67788500	U87	brain:	n/a	n/a
7	BCL3	chr11:67787937-67788806	A549	lung:	n/a	n/a
8	CTCF	chr11:67787920-67788070	GM06990	blood:	n/a	n/a
9	POLR2A	chr11:67788000-67788478	A549	lung:	n/a	n/a
10	RCOR1	chr11:67788009-67788354	Hela-S3	cervix:	n/a	n/a
11	SP1	chr11:67787831-67788505	A549	lung:	n/a	chr11:67788090-67788103
12	EP300	chr11:67787964-67789180	A549	lung:	n/a	n/a
13	MAX	chr11:67787961-67788418	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr11:67787970-67788455	A549	lung:	n/a	n/a
15	RAD21	chr11:67787901-67789135	SK-N-SH	brain:	n/a	chr11:67788491-67788501 chr11:67788246-67788265
16	FOSL2	chr11:67787657-67788632	A549	lung:	n/a	n/a
17	CTCF	chr11:67787373-67789265	SK-N-SH	brain:	n/a	chr11:67788221-67788234 chr11:67788247-67788268 chr11:67788245-67788263 chr11:67788383-67788392 chr11:67788246-67788262
18	POLR2A	chr11:67787903-67789164	A549	lung:	n/a	n/a
19	POLR2A	chr11:67787975-67789157	Hela-S3	cervix:	n/a	n/a
20	REST	chr11:67787870-67788845	A549	lung:	n/a	chr11:67788393-67788411 chr11:67788392-67788412
21	POLR2A	chr11:67787453-67788514	Hela-S3	cervix:	n/a	n/a
22	RAD21	chr11:67788011-67788469	H1-hESC	embryonic stem cell:	n/a	chr11:67788246-67788265
23	CTCF	chr11:67788004-67788455	H1-hESC	embryonic stem cell:	n/a	chr11:67788221-67788234 chr11:67788247-67788268 chr11:67788245-67788263 chr11:67788383-67788392 chr11:67788246-67788262
24	GABPA	chr11:67787984-67788429	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr11:67788022-67788463	HepG2	liver:	n/a	chr11:67788221-67788234 chr11:67788247-67788268 chr11:67788245-67788263 chr11:67788383-67788392 chr11:67788246-67788262
26	MXI1	chr11:67787946-67788553	IMR90	lung:	n/a	chr11:67788489-67788498
27	RAD21	chr11:67788031-67788529	A549	lung:	n/a	chr11:67788491-67788501 chr11:67788246-67788265
28	MAX	chr11:67787863-67789169	A549	lung:	n/a	chr11:67788672-67788682
29	POLR2A	chr11:67787882-67788480	A549	lung:	n/a	n/a
30	SMC3	chr11:67787909-67788609	SK-N-SH	brain:	n/a	chr11:67788247-67788261
31	POLR2A	chr11:67787953-67788540	HL-60	blood:	n/a	n/a
32	RAD21	chr11:67787918-67789187	HCT-116	colon:	n/a	chr11:67788491-67788501 chr11:67788246-67788265
33	CTCF	chr11:67787900-67788050	HMEC	breast:	n/a	n/a
34	CTCF	chr11:67788020-67788474	K562	blood:	n/a	chr11:67788221-67788234 chr11:67788247-67788268 chr11:67788245-67788263 chr11:67788383-67788392 chr11:67788246-67788262
35	TCF7L2	chr11:67788007-67788513	PANC-1	pancreas:	n/a	n/a
36	SMC3	chr11:67787943-67788426	Hela-S3	cervix:	n/a	chr11:67788247-67788261
37	MYC	chr11:67787904-67789132	A549	lung:	n/a	chr11:67788672-67788682
38	TCF12	chr11:67787456-67789224	A549	lung:	n/a	chr11:67787526-67787536
39	MAZ	chr11:67788003-67788427	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr11:67787900-67788050	HCM	heart:	n/a	n/a
41	CTCF	chr11:67787960-67788110	HepG2	liver:	n/a	n/a
42	POLR2A	chr11:67788011-67789130	Hela-S3	cervix:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:67785418..67788114-chr11:67980159..67983027,2	MCF-7	breast:
2	chr11:67787958..67790078-chr11:67980039..67982910,2	MCF-7	breast:
3	chr11:67771065..67771769-chr11:67787544..67788124,2	MCF-7	breast:
4	chr11:67780454..67783992-chr11:67785967..67788810,5	K562	blood:

Variant related genes	Relation type
ALDH3B1	TF binding region
ENSG00000006534	Chromatin interaction
ENSG00000110057	Chromatin interaction
ENSG00000110066	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs11228121	1.00[AFR][1000 genomes]
rs12281209	1.00[AFR][1000 genomes]
rs35880888	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:34 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1036101	chr11:67346813-67828351	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription Genic enhancers 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	139 gene(s)	inside rSNPs	diseases
2	nsv541079	chr11:67346813-67828351	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
3	nsv468606	chr11:67352689-67816936	Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
4	nsv555269	chr11:67352689-67816936	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
5	nsv427892	chr11:67451649-67926562	Bivalent Enhancer Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
6	esv2757450	chr11:67472905-67891289	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	112 gene(s)	inside rSNPs	diseases
7	esv2759835	chr11:67472905-67891289	Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	112 gene(s)	inside rSNPs	diseases
8	nsv428260	chr11:67524937-67797669	Enhancers Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	80 gene(s)	inside rSNPs	diseases
9	esv2758275	chr11:67524937-67859490	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	87 gene(s)	inside rSNPs	diseases
10	nsv469856	chr11:67639037-67859490	Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
11	nsv482760	chr11:67639037-67859490	Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
12	nsv1047567	chr11:67747160-67819790	Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
13	nsv8836	chr11:67752879-67819799	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
14	nsv897836	chr11:67757350-67816936	Enhancers Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
15	nsv897837	chr11:67757350-67821036	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
16	nsv897838	chr11:67757350-67833543	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
17	nsv825963	chr11:67763676-68197054	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	149 gene(s)	inside rSNPs	diseases
18	nsv1050471	chr11:67764068-67821610	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
19	nsv897839	chr11:67765056-67793014	Genic enhancers Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
20	nsv468613	chr11:67765056-67794643	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
21	nsv555277	chr11:67765056-67794643	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
22	nsv468614	chr11:67765056-67799926	ZNF genes & repeats Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
23	nsv897840	chr11:67765056-67804605	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
24	nsv468615	chr11:67765056-67816936	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
25	nsv555278	chr11:67765056-67816936	Enhancers Genic enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription 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	61 gene(s)	inside rSNPs	diseases
26	nsv897841	chr11:67765056-67816936	Bivalent Enhancer Weak transcription Enhancers Strong transcription Active TSS Flanking 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	61 gene(s)	inside rSNPs	diseases
27	nsv469964	chr11:67765056-67821036	Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
28	nsv897842	chr11:67765056-67821036	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
29	nsv897843	chr11:67765056-67833543	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
30	nsv1046054	chr11:67768796-67819790	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	60 gene(s)	inside rSNPs	diseases
31	nsv897844	chr11:67772729-67793014	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
32	nsv897845	chr11:67774231-67821036	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
33	nsv897846	chr11:67776465-67794643	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
34	nsv897847	chr11:67776465-67804605	Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67771600-67797600	Weak transcription	Small Intestine	intestine
2	chr11:67772600-67792400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr11:67782400-67788200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr11:67782400-67791400	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr11:67782400-67794800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr11:67782400-67794800	Strong transcription	Primary neutrophils fromperipheralblood	blood
7	chr11:67782400-67796800	Weak transcription	Colon Smooth Muscle	Colon
8	chr11:67782600-67789000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:67782600-67791400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr11:67782600-67791600	Weak transcription	Ovary	ovary
11	chr11:67782600-67791600	Weak transcription	Stomach Smooth Muscle	stomach
12	chr11:67782600-67792200	Weak transcription	HSMMtube	muscle
13	chr11:67782600-67792600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr11:67782600-67794000	Weak transcription	NH-A	brain
15	chr11:67782600-67797000	Weak transcription	Rectal Smooth Muscle	rectum
16	chr11:67782800-67795800	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr11:67782800-67797200	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr11:67784000-67789200	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr11:67784600-67788200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr11:67784600-67788200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr11:67784800-67788200	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr11:67784800-67788200	Weak transcription	Stomach Mucosa	stomach
23	chr11:67784800-67789000	Weak transcription	Duodenum Mucosa	Duodenum
24	chr11:67784800-67791400	Weak transcription	Osteobl	bone
25	chr11:67784800-67791600	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr11:67785000-67788200	Weak transcription	Fetal Intestine Large	intestine
27	chr11:67785000-67788400	Weak transcription	Fetal Heart	heart
28	chr11:67785000-67791200	Weak transcription	NHDF-Ad	bronchial
29	chr11:67785000-67792600	Weak transcription	Left Ventricle	heart
30	chr11:67785200-67788200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr11:67785200-67788200	Weak transcription	Fetal Muscle Leg	muscle
32	chr11:67785200-67788200	Weak transcription	HMEC	breast
33	chr11:67785200-67797200	Weak transcription	Right Atrium	heart
34	chr11:67785400-67795800	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr11:67785600-67788200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr11:67785600-67788200	Weak transcription	Brain Anterior Caudate	brain
37	chr11:67785600-67788400	Genic enhancers	A549	lung
38	chr11:67785600-67788600	Weak transcription	Fetal Lung	lung
39	chr11:67785600-67789400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr11:67785600-67792200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr11:67785600-67792400	Weak transcription	Brain Cingulate Gyrus	brain
42	chr11:67785600-67796000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr11:67785600-67797600	Weak transcription	Brain Substantia Nigra	brain
44	chr11:67785800-67788600	Weak transcription	Liver	Liver
45	chr11:67785800-67791600	Weak transcription	Brain Hippocampus Middle	brain
46	chr11:67785800-67794800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr11:67786000-67788200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr11:67786000-67788200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr11:67786000-67788200	Weak transcription	Gastric	stomach
50	chr11:67786400-67788200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin

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