Variant report

Variant	rs1151520
Chromosome Location	chr11:65659813-65659814
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:120)
CpG islands
(count:61)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:65657750-65661000	K562	blood:	n/a	n/a
2	POLR2A	chr11:65657347-65660286	HepG2	liver:	n/a	n/a
3	SIN3AK20	chr11:65657618-65659903	HCT-116	colon:	n/a	n/a
4	CTCF	chr11:65659680-65659830	HCPEpiC	choroid plexus:	n/a	n/a
5	POLR2A	chr11:65657492-65660848	GM12891	blood:	n/a	n/a
6	POLR2A	chr11:65659740-65660084	GM12878	blood:	n/a	n/a
7	POU2F2	chr11:65659176-65660722	GM12878	blood:	n/a	n/a
8	POLR2A	chr11:65657769-65660331	K562	blood:	n/a	n/a
9	POLR2A	chr11:65654632-65669034	U87	brain:	n/a	n/a
10	POLR2A	chr11:65657733-65661893	SK-N-MC	brain:	n/a	n/a
11	PBX3	chr11:65657625-65660136	A549	lung:	n/a	n/a
12	UBTF	chr11:65657777-65659843	K562	blood:	n/a	n/a
13	POLR2A	chr11:65657516-65662050	K562	blood:	n/a	n/a
14	EGR1	chr11:65659738-65660006	K562	blood:	n/a	n/a
15	POLR2A	chr11:65657936-65661092	Hela-S3	cervix:	n/a	n/a
16	NFYB	chr11:65659669-65660019	GM12878	blood:	n/a	n/a
17	POLR2A	chr11:65655144-65662194	HUVEC	blood vessel:	n/a	n/a
18	POLR2A	chr11:65657409-65662237	HCT-116	colon:	n/a	n/a
19	PML	chr11:65657441-65661967	GM12878	blood:	n/a	n/a
20	SIN3AK20	chr11:65657191-65661090	PANC-1	pancreas:	n/a	n/a
21	ETS1	chr11:65657668-65660023	K562	blood:	n/a	chr11:65659355-65659368 chr11:65659357-65659368 chr11:65659356-65659370
22	TEAD4	chr11:65657196-65660349	K562	blood:	n/a	n/a
23	TRIM28	chr11:65657673-65660126	K562	blood:	n/a	n/a
24	GATA2	chr11:65657750-65659962	HUVEC	blood vessel:	n/a	chr11:65659559-65659573
25	POLR2A	chr11:65659744-65660561	HUVEC	blood vessel:	n/a	n/a
26	POLR2A	chr11:65657731-65661298	GM12878	blood:	n/a	n/a
27	POLR2A	chr11:65657295-65662093	PFSK-1	brain:	n/a	n/a
28	HEY1	chr11:65657685-65660821	K562	blood:	n/a	n/a
29	POLR2A	chr11:65657671-65660085	H1-hESC	embryonic stem cell:	n/a	n/a
30	HCFC1	chr11:65657083-65660476	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr11:65655457-65664831	A549	lung:	n/a	n/a
32	POLR2A	chr11:65657527-65662177	K562	blood:	n/a	n/a
33	POLR2A	chr11:65658966-65659950	HepG2	liver:	n/a	n/a
34	POLR2A	chr11:65658913-65660793	GM12878	blood:	n/a	n/a
35	TAF1	chr11:65659725-65659979	K562	blood:	n/a	n/a
36	ZC3H11A	chr11:65659689-65659853	K562	blood:	n/a	n/a
37	BCL3	chr11:65657463-65660696	A549	lung:	n/a	chr11:65659422-65659430
38	POLR2A	chr11:65659765-65660015	MCF-7	breast:	n/a	n/a
39	POLR2A	chr11:65659735-65660046	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr11:65655528-65662097	GM12892	blood:	n/a	n/a
41	POLR2A	chr11:65657589-65661069	ProgFib	skin:	n/a	n/a
42	HEY1	chr11:65657704-65662165	K562	blood:	n/a	n/a
43	POLR2A	chr11:65657476-65661952	HepG2	liver:	n/a	n/a
44	POLR2A	chr11:65659740-65660085	A549	lung:	n/a	n/a
45	SIN3AK20	chr11:65657543-65659963	HCT-116	colon:	n/a	n/a
46	CBX3	chr11:65657785-65660370	K562	blood:	n/a	n/a
47	POLR2A	chr11:65659244-65660703	GM12878	blood:	n/a	n/a
48	PML	chr11:65657247-65660092	K562	blood:	n/a	n/a
49	MAZ	chr11:65654781-65660027	IMR90	lung:	n/a	chr11:65658152-65658161 chr11:65658196-65658205 chr11:65655739-65655749
50	POLR2A	chr11:65654791-65669084	U87	brain:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:65659772-65659822	IMR90	lung:	fetal
2	chr11:65659772-65659822	HMEC	breast:	n/a
3	chr11:65659772-65659822	NT2-D1	testis:	n/a
4	chr11:65659772-65659822	HRCEpiC	kidney:	n/a
5	chr11:65659772-65659822	U87	brain:	n/a
6	chr11:65659772-65659822	GM06990	blood:	n/a
7	chr11:65659772-65659822	AG04449	skin:	fetal
8	chr11:65659772-65659822	HepG2	liver:	n/a
9	chr11:65659772-65659822	T-47D	breast:	n/a
10	chr11:65659772-65659822	SKMC	muscle:	n/a
11	chr11:65659772-65659822	SK-N-SH	brain:	n/a
12	chr11:65659772-65659822	ECC-1	luminal epithelium:	n/a
13	chr11:65659772-65659822	HIPEpiC	eye:	n/a
14	chr11:65659772-65659822	ProgFib	skin:	n/a
15	chr11:65659772-65659822	RPTEC	kidney:	n/a
16	chr11:65659772-65659822	NB4	blood:	n/a
17	chr11:65659772-65659822	SK-N-SH_RA	brain:	n/a
18	chr11:65659772-65659822	CMK	blood:	n/a
19	chr11:65659772-65659822	HPAEpiC	pulmonary alveolar:	n/a
20	chr11:65659772-65659822	H1-hESC	embryonic stem cell:	embryo
21	chr11:65659772-65659822	Jurkat	blood:	n/a
22	chr11:65659772-65659822	MCF10A-Er-Src	breast:	n/a
23	chr11:65659772-65659822	AG10803	skin:	n/a
24	chr11:65659772-65659822	BJ	skin:	n/a
25	chr11:65659772-65659822	GM12891	blood:	n/a
26	chr11:65659772-65659822	NHDF-neo	bronchial:	n/a
27	chr11:65659772-65659822	HRE	kidney:	n/a
28	chr11:65659772-65659822	GM12892	blood:	n/a
29	chr11:65659772-65659822	HAEpiC	amniotic membrane:	n/a
30	chr11:65659772-65659822	LNCaP	prostate:	n/a
31	chr11:65659772-65659822	HEEpiC	esophagus:	n/a
32	chr11:65659772-65659822	AoSMC	blood vessel:	n/a
33	chr11:65659772-65659822	AG09309	skin:	n/a
34	chr11:65659772-65659822	NHBE	bronchial:	n/a
35	chr11:65659772-65659822	HL-60	blood:	n/a
36	chr11:65659772-65659822	ovcar-3	ovarian:	n/a
37	chr11:65659772-65659822	AG04450	lung:	fetal
38	chr11:65659772-65659822	PANC-1	pancreas:	n/a
39	chr11:65659772-65659822	Hepatocyte	liver:	n/a
40	chr11:65659772-65659822	MCF-7	breast:	n/a
41	chr11:65659772-65659822	HEK293	kidney:	embryo
42	chr11:65659772-65659822	GM19239	blood:	n/a
43	chr11:65659772-65659822	HNPCEpiC	eye:	n/a
44	chr11:65659772-65659822	SAEC	small airway:	n/a
45	chr11:65659772-65659822	HCPEpiC	choroid plexus:	n/a
46	chr11:65659772-65659822	A549	lung:	n/a
47	chr11:65659772-65659822	HUVEC	blood vessel:	n/a
48	chr11:65659772-65659822	HCT-116	colon:	n/a
49	chr11:65659772-65659822	NH-A	brain:	n/a
50	chr11:65659772-65659822	AG09319	gingival:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:65190823..65192325-chr11:65659028..65661799,2	K562	blood:
2	chr11:65465574..65468849-chr11:65659509..65661845,3	K562	blood:
3	chr11:65657107..65659864-chr11:66036057..66038289,3	MCF-7	breast:
4	chr11:65650800..65661192-chr11:65726307..65736419,31	MCF-7	breast:
5	chr11:65512196..65514040-chr11:65659472..65661075,2	K562	blood:
6	chr11:65382961..65385315-chr11:65657365..65660183,3	K562	blood:
7	chr11:65654573..65660022-chr11:65726606..65732418,16	MCF-7	breast:
8	chr11:65650579..65663306-chr11:65677153..65690311,39	MCF-7	breast:
9	chr11:65659026..65661070-chr11:65896496..65899355,2	K562	blood:
10	chr11:65268166..65268701-chr11:65659614..65660338,2	Hela-S3	cervix:
11	chr11:65658134..65659956-chr11:66102829..66104938,2	K562	blood:
12	chr11:65397014..65399250-chr11:65658274..65660177,2	K562	blood:
13	chr11:65658275..65660605-chr5:137804830..137807316,2	K562	blood:
14	chr11:65574802..65576504-chr11:65658689..65661475,2	K562	blood:
15	chr11:65654924..65661575-chr11:65833688..65838665,10	K562	blood:
16	chr11:65478350..65482284-chr11:65653854..65660529,8	K562	blood:
17	chr11:65492420..65494936-chr11:65657867..65659851,2	K562	blood:
18	chr11:65654924..65660442-chr11:65834310..65838665,6	K562	blood:
19	chr11:65657526..65660220-chr11:65812973..65815737,3	MCF-7	breast:
20	chr11:65472457..65475716-chr11:65659486..65662901,4	K562	blood:
21	chr11:65477188..65481209-chr11:65654091..65661409,11	K562	blood:
22	chr11:65567188..65568859-chr11:65658310..65660115,2	K562	blood:
23	chr11:65479676..65481721-chr11:65658837..65660766,2	MCF-7	breast:
24	chr1:156469829..156471624-chr11:65658653..65660354,2	K562	blood:
25	chr11:65421851..65424621-chr11:65658230..65660930,2	K562	blood:
26	chr11:65646632..65650808-chr11:65654844..65660529,6	MCF-7	breast:

No data

Variant related genes	Relation type
FIBP	TF binding region
FIBP	CpG island
ENSG00000175550	Chromatin interaction
ENSG00000175115	Chromatin interaction
ENSG00000175229	Chromatin interaction
ENSG00000172543	Chromatin interaction
ENSG00000255557	Chromatin interaction
ENSG00000175467	Chromatin interaction
ENSG00000255038	Chromatin interaction
ENSG00000214659	Chromatin interaction
ENSG00000172977	Chromatin interaction
ENSG00000116604	Chromatin interaction
ENSG00000174791	Chromatin interaction
ENSG00000197136	Chromatin interaction
ENSG00000174903	Chromatin interaction
ENSG00000175573	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1048924	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10896054	1.00[EUR][1000 genomes]
rs12275175	1.00[EUR][1000 genomes]
rs12283972	1.00[EUR][1000 genomes]
rs12294096	1.00[EUR][1000 genomes]
rs12294241	1.00[EUR][1000 genomes]
rs12294549	1.00[EUR][1000 genomes]
rs1647569	1.00[EUR][1000 genomes]
rs34035680	1.00[EUR][1000 genomes]
rs35194319	1.00[EUR][1000 genomes]
rs500667	1.00[EUR][1000 genomes]
rs508328	1.00[EUR][1000 genomes]
rs516889	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs548709	1.00[EUR][1000 genomes]
rs551115	1.00[EUR][1000 genomes]
rs551986	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs558167	1.00[AMR][1000 genomes]
rs56663613	1.00[EUR][1000 genomes]
rs56990327	1.00[EUR][1000 genomes]
rs601314	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs604630	0.92[ASW][hapmap];0.87[LWK][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs613953	1.00[EUR][1000 genomes]
rs614330	1.00[EUR][1000 genomes]
rs641323	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs645043	0.81[AFR][1000 genomes]
rs669300	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs7107453	1.00[TSI][hapmap]
rs7115662	1.00[EUR][1000 genomes]
rs7124858	1.00[EUR][1000 genomes]
rs73492420	1.00[EUR][1000 genomes]
rs73492424	1.00[EUR][1000 genomes]
rs73492432	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897736	chr11:65335705-65676516	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' 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	227 gene(s)	inside rSNPs	diseases
2	nsv430401	chr11:65419324-65788024	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
3	esv2758274	chr11:65559893-65722363	Genic enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription 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 target site	178 gene(s)	inside rSNPs	diseases
4	esv2759834	chr11:65559893-65722363	Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers 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	178 gene(s)	inside rSNPs	diseases
5	nsv427890	chr11:65559893-65722363	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Genic enhancers 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 target site	178 gene(s)	inside rSNPs	diseases
6	nsv897761	chr11:65580638-65738566	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	186 gene(s)	inside rSNPs	diseases
7	nsv555215	chr11:65581579-65676516	Strong transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers 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	165 gene(s)	inside rSNPs	diseases
8	nsv897762	chr11:65613218-65758854	Active TSS Flanking Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	185 gene(s)	inside rSNPs	diseases
9	nsv897764	chr11:65613348-65695222	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
10	nsv897765	chr11:65623708-65758854	Strong transcription Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
11	nsv832191	chr11:65632329-65806120	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
12	nsv530622	chr11:65649068-65661361	Genic enhancers Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	65 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs1151520	CCDC85B	cis	lymphoblastoid	seeQTL
rs1151520	CCDC85B	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65655000-65660200	Flanking Active TSS	Stomach Smooth Muscle	stomach
2	chr11:65655000-65662200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr11:65656200-65660000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
4	chr11:65656200-65660200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
5	chr11:65656200-65660200	Flanking Active TSS	Dnd41	blood
6	chr11:65656200-65660800	Flanking Active TSS	Adipose Nuclei	Adipose
7	chr11:65656200-65662200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr11:65657800-65660000	Active TSS	Brain Inferior Temporal Lobe	brain
9	chr11:65657800-65661200	Active TSS	Psoas Muscle	Psoas
10	chr11:65658000-65660000	Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr11:65658200-65660000	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
12	chr11:65658200-65660000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
13	chr11:65658200-65660400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
14	chr11:65658200-65662000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr11:65658400-65660000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr11:65658600-65660000	Enhancers	Fetal Brain Male	brain
17	chr11:65658600-65660000	Enhancers	Stomach Mucosa	stomach
18	chr11:65658600-65660400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
19	chr11:65658600-65660600	Flanking Active TSS	Fetal Brain Female	brain
20	chr11:65658600-65660600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
21	chr11:65658600-65662000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
22	chr11:65658600-65662200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr11:65658800-65660600	Flanking Active TSS	Brain Hippocampus Middle	brain
24	chr11:65658800-65660800	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr11:65658800-65662000	Transcr. at gene 5' and 3'	NHLF	lung
26	chr11:65659000-65660000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr11:65659000-65660200	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr11:65659000-65660400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
29	chr11:65659000-65660400	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
30	chr11:65659000-65660600	Transcr. at gene 5' and 3'	NHEK	skin
31	chr11:65659000-65660800	Transcr. at gene 5' and 3'	Osteobl	bone
32	chr11:65659000-65662200	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
33	chr11:65659000-65662200	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr11:65659000-65662200	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr11:65659200-65660000	Flanking Active TSS	Primary T cells from cord blood	blood
36	chr11:65659200-65660000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
37	chr11:65659200-65660200	Transcr. at gene 5' and 3'	A549	lung
38	chr11:65659200-65660400	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
39	chr11:65659200-65660600	Enhancers	Pancreas	Pancrea
40	chr11:65659200-65660600	Flanking Active TSS	Rectal Smooth Muscle	rectum
41	chr11:65659200-65661400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr11:65659200-65661800	Flanking Active TSS	Brain Cingulate Gyrus	brain
43	chr11:65659200-65662200	Transcr. at gene 5' and 3'	Breast Myoepithelial Primary Cells	Breast
44	chr11:65659400-65660000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr11:65659400-65660000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr11:65659400-65660000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
47	chr11:65659400-65660000	Enhancers	Gastric	stomach
48	chr11:65659400-65660000	Transcr. at gene 5' and 3'	NH-A	brain
49	chr11:65659400-65660200	Flanking Active TSS	Fetal Stomach	stomach
50	chr11:65659400-65660200	Transcr. at gene 5' and 3'	HUVEC	blood vessel

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