Variant report

Variant	rs659622
Chromosome Location	chr11:107328956-107328957
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:98)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:98 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ELF1	chr11:107328221-107329162	HCT-116	colon:	n/a	n/a
2	POLR2A	chr11:107328017-107329055	GM15510	blood:	n/a	n/a
3	POLR2A	chr11:107328208-107328990	PANC-1	pancreas:	n/a	n/a
4	GTF2F1	chr11:107328285-107329066	Hela-S3	cervix:	n/a	n/a
5	TCF12	chr11:107328214-107329050	A549	lung:	n/a	chr11:107328979-107328986
6	POLR2A	chr11:107328224-107329006	GM12878	blood:	n/a	n/a
7	POLR2A	chr11:107328175-107329068	GM12878	blood:	n/a	n/a
8	POLR2A	chr11:107328024-107328993	K562	blood:	n/a	n/a
9	YY1	chr11:107327836-107329046	SK-N-SH	brain:	n/a	n/a
10	ELF1	chr11:107328206-107329164	GM12878	blood:	n/a	n/a
11	RCOR1	chr11:107327948-107329118	K562	blood:	n/a	n/a
12	REST	chr11:107328010-107329012	H1-neurons	neurons:	n/a	n/a
13	REST	chr11:107328066-107329007	HL-60	blood:	n/a	n/a
14	ELF1	chr11:107328354-107329023	HepG2	liver:	n/a	n/a
15	POLR2A	chr11:107328332-107329052	HEK293	kidney:	n/a	n/a
16	MAFK	chr11:107328378-107329034	K562	blood:	n/a	n/a
17	MAX	chr11:107328253-107329009	SK-N-SH	brain:	n/a	n/a
18	TAF7	chr11:107328060-107328969	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr11:107327922-107329078	Raji	blood:	n/a	n/a
20	CTCF	chr11:107328860-107329010	GM12864	blood:	n/a	n/a
21	POLR2A	chr11:107328343-107328968	SK-N-MC	brain:	n/a	n/a
22	POLR2A	chr11:107327943-107329117	GM12878	blood:	n/a	n/a
23	POLR2A	chr11:107327938-107328968	PBDE	blood:	n/a	n/a
24	POLR2A	chr11:107327898-107329005	HepG2	liver:	n/a	n/a
25	POLR2A	chr11:107327977-107329005	GM19193	blood:	n/a	n/a
26	TAF1	chr11:107328023-107329080	H1-hESC	embryonic stem cell:	n/a	n/a
27	TAF1	chr11:107328281-107329041	SK-N-SH	brain:	n/a	n/a
28	POLR2A	chr11:107328325-107329193	HCT-116	colon:	n/a	n/a
29	ZMIZ1	chr11:107328362-107328993	K562	blood:	n/a	n/a
30	HCFC1	chr11:107328045-107328999	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr11:107327940-107329347	GM12891	blood:	n/a	n/a
32	MAX	chr11:107328250-107329001	ECC-1	luminal epithelium:	n/a	n/a
33	HEY1	chr11:107328282-107328982	HepG2	liver:	n/a	n/a
34	RELA	chr11:107328288-107329056	GM18951	blood:	n/a	n/a
35	ELF1	chr11:107328162-107329189	HCT-116	colon:	n/a	n/a
36	SIN3A	chr11:107327849-107329062	H1-hESC	embryonic stem cell:	n/a	n/a
37	ELF1	chr11:107328292-107329008	HepG2	liver:	n/a	n/a
38	YY1	chr11:107328112-107328972	GM12878	blood:	n/a	n/a
39	POLR2A	chr11:107328309-107329138	U87	brain:	n/a	n/a
40	POLR2A	chr11:107327989-107329132	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr11:107328295-107329042	ProgFib	skin:	n/a	n/a
42	TBP	chr11:107327792-107329016	H1-hESC	embryonic stem cell:	n/a	n/a
43	MBD4	chr11:107328243-107328976	HepG2	liver:	n/a	n/a
44	MAX	chr11:107328341-107329066	SK-N-SH	brain:	n/a	n/a
45	WRNIP1	chr11:107328064-107329079	GM12878	blood:	n/a	n/a
46	RCOR1	chr11:107328122-107329004	Hela-S3	cervix:	n/a	n/a
47	TBL1XR1	chr11:107328221-107329076	GM12878	blood:	n/a	n/a
48	ELF1	chr11:107328238-107329045	MCF-7	breast:	n/a	n/a
49	POLR2A	chr11:107327961-107329028	PFSK-1	brain:	n/a	n/a
50	KAP1	chr11:107328092-107329062	HEK293	kidney:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:107328914-107328964	A549	lung:	n/a
2	chr11:107328914-107328964	H1-hESC	embryonic stem cell:	embryo
3	chr11:107328914-107328964	MCF10A-Er-Src	breast:	n/a
4	chr11:107328914-107328964	SK-N-SH_RA	brain:	n/a
5	chr11:107328914-107328964	HEK293	kidney:	embryo
6	chr11:107328914-107328964	GM12891	blood:	n/a
7	chr11:107328914-107328964	ECC-1	luminal epithelium:	n/a
8	chr11:107328914-107328964	HRCEpiC	kidney:	n/a
9	chr11:107328914-107328964	HMEC	breast:	n/a
10	chr11:107328914-107328964	LNCaP	prostate:	n/a
11	chr11:107328914-107328964	AG04450	lung:	fetal
12	chr11:107328914-107328964	ovcar-3	ovarian:	n/a
13	chr11:107328914-107328964	AG04449	skin:	fetal
14	chr11:107328914-107328964	GM06990	blood:	n/a
15	chr11:107328914-107328964	K562	blood:	n/a
16	chr11:107328914-107328964	PFSK-1	brain:	n/a
17	chr11:107328914-107328964	GM19239	blood:	n/a
18	chr11:107328914-107328964	SAEC	small airway:	n/a
19	chr11:107328914-107328964	T-47D	breast:	n/a
20	chr11:107328914-107328964	HAEpiC	amniotic membrane:	n/a
21	chr11:107328914-107328964	HCPEpiC	choroid plexus:	n/a
22	chr11:107328914-107328964	NHDF-neo	bronchial:	n/a
23	chr11:107328914-107328964	HL-60	blood:	n/a
24	chr11:107328914-107328964	HRPEpiC	eye:	n/a
25	chr11:107328914-107328964	HIPEpiC	eye:	n/a
26	chr11:107328914-107328964	AG10803	skin:	n/a
27	chr11:107328914-107328964	CMK	blood:	n/a
28	chr11:107328914-107328964	HEEpiC	esophagus:	n/a
29	chr11:107328914-107328964	HCT-116	colon:	n/a
30	chr11:107328914-107328964	HepG2	liver:	n/a
31	chr11:107328914-107328964	NT2-D1	testis:	n/a
32	chr11:107328914-107328964	BJ	skin:	n/a
33	chr11:107328914-107328964	GM12892	blood:	n/a
34	chr11:107328914-107328964	HUVEC	blood vessel:	n/a
35	chr11:107328914-107328964	NHBE	bronchial:	n/a
36	chr11:107328914-107328964	HCF	heart:	n/a
37	chr11:107328914-107328964	Hepatocyte	liver:	n/a
38	chr11:107328914-107328964	HPAEpiC	pulmonary alveolar:	n/a
39	chr11:107328914-107328964	NH-A	brain:	n/a
40	chr11:107328914-107328964	Caco-2	colon:	n/a
41	chr11:107328914-107328964	Hela-S3	cervix:	n/a
42	chr11:107328914-107328964	ProgFib	skin:	n/a
43	chr11:107328914-107328964	PrEC	prostate:	n/a
44	chr11:107328914-107328964	SK-N-SH	brain:	n/a
45	chr11:107328914-107328964	IMR90	lung:	fetal
46	chr11:107328914-107328964	AoSMC	blood vessel:	n/a
47	chr11:107328914-107328964	U87	brain:	n/a
48	chr11:107328914-107328964	SK-N-MC	brain:	n/a
49	chr11:107328914-107328964	HCM	heart:	n/a
50	chr11:107328914-107328964	SKMC	muscle:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:107311896..107313858-chr11:107327138..107329604,2	K562	blood:
2	chr11:107328376..107329012-chr20:10654520..10655433,2	HCT-116	colon:

No data

Variant related genes	Relation type
CWF19L2	TF binding region
CWF19L2	CpG island
ENSG00000152404	Chromatin interaction
ENSG00000101384	Chromatin interaction

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10502092	0.82[CHB][hapmap]
rs10749892	0.82[AMR][1000 genomes]
rs10789591	0.82[AMR][1000 genomes]
rs10789595	0.81[AMR][1000 genomes]
rs10789596	0.82[AMR][1000 genomes]
rs10890735	0.87[CHB][hapmap]
rs11212274	0.82[CHB][hapmap]
rs11212277	0.87[CHB][hapmap]
rs12577299	0.82[CHB][hapmap]
rs2037826	0.87[CHB][hapmap]
rs2113926	0.82[AMR][1000 genomes]
rs2113927	0.82[AMR][1000 genomes]
rs2355841	0.82[AMR][1000 genomes]
rs2355842	0.82[AMR][1000 genomes]
rs2432869	0.95[CEU][hapmap];0.86[JPT][hapmap]
rs2883633	0.82[AMR][1000 genomes]
rs473520	0.86[CEU][hapmap];0.80[JPT][hapmap]
rs4754208	0.82[AMR][1000 genomes]
rs4754212	0.82[AMR][1000 genomes]
rs478067	0.95[CEU][hapmap];0.87[JPT][hapmap];0.83[AMR][1000 genomes]
rs478815	0.83[AMR][1000 genomes]
rs501088	0.82[AMR][1000 genomes]
rs510743	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs512574	0.89[CEU][hapmap];0.87[JPT][hapmap];0.81[AMR][1000 genomes]
rs525996	0.95[CEU][hapmap];0.86[JPT][hapmap]
rs533703	0.82[AMR][1000 genomes]
rs537341	0.83[AMR][1000 genomes]
rs541277	0.82[AMR][1000 genomes]
rs550882	0.81[AMR][1000 genomes]
rs551168	0.95[CEU][hapmap];0.87[JPT][hapmap]
rs556528	0.80[JPT][hapmap];0.83[AMR][1000 genomes]
rs557972	0.82[AMR][1000 genomes]
rs559269	0.81[CEU][hapmap];0.87[JPT][hapmap];0.82[AMR][1000 genomes]
rs559959	0.83[AMR][1000 genomes]
rs574014	0.94[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs574879	0.80[CEU][hapmap]
rs580224	0.80[CEU][hapmap]
rs580913	0.95[CEU][hapmap];0.87[JPT][hapmap]
rs594772	0.82[AMR][1000 genomes]
rs602628	0.82[AMR][1000 genomes]
rs603487	0.95[CEU][hapmap];0.87[JPT][hapmap];0.81[AMR][1000 genomes]
rs604211	0.95[CEU][hapmap];0.87[JPT][hapmap];0.83[AMR][1000 genomes]
rs607151	0.95[CEU][hapmap];0.81[AMR][1000 genomes]
rs610203	0.81[AMR][1000 genomes]
rs615998	0.82[AMR][1000 genomes]
rs621677	0.95[CEU][hapmap];0.85[JPT][hapmap];0.81[AMR][1000 genomes]
rs622862	0.80[CEU][hapmap]
rs628513	0.83[AMR][1000 genomes]
rs636080	0.80[CEU][hapmap]
rs639437	0.95[CEU][hapmap];0.86[JPT][hapmap]
rs650699	0.95[CEU][hapmap];0.87[JPT][hapmap]
rs651620	0.95[CEU][hapmap];0.87[JPT][hapmap]
rs6588961	0.82[AMR][1000 genomes]
rs661889	0.80[CEU][hapmap];0.87[JPT][hapmap];0.83[AMR][1000 genomes]
rs682042	0.95[CEU][hapmap];0.87[JPT][hapmap];0.83[AMR][1000 genomes]
rs682590	0.95[CEU][hapmap];0.87[JPT][hapmap];0.81[AMR][1000 genomes]
rs686806	0.94[CEU][hapmap];0.87[JPT][hapmap];0.83[AMR][1000 genomes]
rs7115296	0.82[AMR][1000 genomes]
rs7127931	0.82[AMR][1000 genomes]
rs7131186	0.82[AMR][1000 genomes]
rs7931852	0.82[AMR][1000 genomes]
rs7932042	0.82[AMR][1000 genomes]
rs7932991	0.82[AMR][1000 genomes]
rs7938897	0.82[AMR][1000 genomes]
rs7945258	0.81[AMR][1000 genomes]
rs7945936	0.82[AMR][1000 genomes]
rs7946787	0.82[AMR][1000 genomes]
rs90623	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898365	chr11:106944975-107430300	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv898366	chr11:106944975-107433835	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv898367	chr11:106944975-107443420	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv898369	chr11:106958304-107443420	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv898370	chr11:107027991-107430300	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv898372	chr11:107049968-107433835	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1038368	chr11:107116577-107664181	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
8	nsv541163	chr11:107116577-107664181	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
9	nsv898373	chr11:107124903-107433835	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	esv2756363	chr11:107189790-107376790	ZNF genes & repeats Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
11	nsv556376	chr11:107250851-107486598	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
12	nsv898375	chr11:107299631-107365191	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
13	nsv898376	chr11:107299631-107443420	Weak transcription Active TSS Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	nsv898377	chr11:107316499-107354312	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
15	esv2757476	chr11:107324276-107344568	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
16	esv2759864	chr11:107324276-107344568	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107326800-107329000	Active TSS	iPS-18 Cell Line	embryonic stem cell
2	chr11:107326800-107329200	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr11:107326800-107329200	Active TSS	HUES64 Cell Line	embryonic stem cell
4	chr11:107326800-107329200	Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr11:107326800-107329400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr11:107326800-107329400	Active TSS	GM12878-XiMat	blood
7	chr11:107327000-107329000	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr11:107327000-107329200	Active TSS	K562	blood
9	chr11:107327200-107329200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr11:107327400-107329000	Active TSS	HSMM	muscle
11	chr11:107327400-107329200	Active TSS	H1 Cell Line	embryonic stem cell
12	chr11:107327400-107329200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr11:107327400-107329200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr11:107327400-107329200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr11:107327400-107329200	Active TSS	Psoas Muscle	Psoas
16	chr11:107327400-107329200	Active TSS	A549	lung
17	chr11:107327400-107329400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr11:107327600-107329000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr11:107327600-107329000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr11:107327600-107329000	Active TSS	Brain Hippocampus Middle	brain
21	chr11:107327600-107329000	Active TSS	Rectal Smooth Muscle	rectum
22	chr11:107327600-107329000	Active TSS	Skeletal Muscle Male	skeletal muscle
23	chr11:107327600-107329000	Active TSS	NHEK	skin
24	chr11:107327600-107329200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr11:107327600-107329200	Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr11:107327600-107329200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
27	chr11:107327600-107329200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr11:107327600-107329200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr11:107327600-107329200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
30	chr11:107327600-107329200	Active TSS	Fetal Brain Male	brain
31	chr11:107327600-107329200	Active TSS	Fetal Muscle Trunk	muscle
32	chr11:107327600-107329200	Active TSS	Ovary	ovary
33	chr11:107327600-107329200	Active TSS	Thymus	Thymus
34	chr11:107327600-107329200	Active TSS	NHDF-Ad	bronchial
35	chr11:107327600-107329200	Active TSS	NHLF	lung
36	chr11:107327600-107329400	Active TSS	Right Atrium	heart
37	chr11:107327800-107329000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
38	chr11:107327800-107329000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr11:107327800-107329000	Active TSS	H9 Cell Line	embryonic stem cell
40	chr11:107327800-107329000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr11:107327800-107329200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr11:107327800-107329200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
43	chr11:107327800-107329200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr11:107327800-107329200	Active TSS	Aorta	Aorta
45	chr11:107327800-107329200	Active TSS	Brain Germinal Matrix	brain
46	chr11:107327800-107329200	Active TSS	Colonic Mucosa	Colon
47	chr11:107327800-107329200	Active TSS	Fetal Intestine Large	intestine
48	chr11:107327800-107329200	Active TSS	Fetal Intestine Small	intestine
49	chr11:107327800-107329200	Active TSS	Pancreatic Islets	Pancreatic Islet
50	chr11:107327800-107329200	Active TSS	Fetal Lung	lung

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