Variant report

Variant	rs3751855
Chromosome Location	chr16:31091209-31091210
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:31090778..31094988-chr16:31190438..31192944,4	K562	blood:
2	chr16:30995095..30997179-chr16:31088575..31091751,4	MCF-7	breast:
3	chr16:31091019..31091656-chr16:31107126..31107712,2	MCF-7	breast:
4	chr16:31088446..31092085-chr16:31188490..31191515,3	K562	blood:
5	chr16:31089101..31091709-chr16:31454244..31455871,2	K562	blood:
6	chr16:30967737..30970640-chr16:31089568..31092427,3	K562	blood:

Variant related genes	Relation type
ENSG00000167397	Chromatin interaction
ENSG00000099377	Chromatin interaction
ENSG00000089280	Chromatin interaction
ENSG00000176723	Chromatin interaction
ENSG00000099381	Chromatin interaction

Extended variants
information (count: 152 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:140)

rs_ID	r²[population]
rs1046276	1.00[JPT][hapmap]
rs1060506	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10782001	0.89[JPT][hapmap]
rs10782002	0.89[JPT][hapmap]
rs10871454	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11076	0.88[JPT][hapmap]
rs1108431	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11150599	0.88[JPT][hapmap]
rs11150600	0.89[JPT][hapmap]
rs11150601	0.87[CEU][hapmap];0.89[JPT][hapmap]
rs11150604	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11640534	0.89[JPT][hapmap]
rs11640767	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11640957	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11640961	0.89[JPT][hapmap]
rs11642003	0.82[ASN][1000 genomes]
rs11642192	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11647284	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11647442	0.95[ASN][1000 genomes]
rs11649653	1.00[JPT][hapmap]
rs11862744	0.91[CEU][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11864806	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11864839	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11865038	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11865499	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12102776	0.82[CHB][hapmap]
rs12445568	0.87[CEU][hapmap]
rs12445650	0.92[CEU][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12448321	0.89[ASN][1000 genomes]
rs12597511	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs12716981	0.95[ASN][1000 genomes]
rs12716982	0.95[ASN][1000 genomes]
rs12924903	1.00[JPT][hapmap]
rs12928852	0.89[JPT][hapmap]
rs12931046	0.83[CEU][hapmap];0.89[JPT][hapmap]
rs12934418	0.89[ASN][1000 genomes]
rs13708	0.88[CEU][hapmap];0.89[JPT][hapmap]
rs14235	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1458201	0.89[JPT][hapmap]
rs1458202	0.89[JPT][hapmap]
rs1549293	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs17839567	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17839568	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1870293	0.87[CEU][hapmap];0.89[JPT][hapmap]
rs1978485	0.95[ASN][1000 genomes]
rs1978487	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2032915	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2054213	0.87[CEU][hapmap];0.89[JPT][hapmap]
rs2288004	0.89[ASN][1000 genomes]
rs2303222	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2303223	1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2305880	0.87[CEU][hapmap];0.89[JPT][hapmap]
rs2305884	0.87[CEU][hapmap];0.89[JPT][hapmap]
rs2359612	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2855475	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs28725459	0.91[ASN][1000 genomes]
rs28814987	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2884738	0.95[ASN][1000 genomes]
rs34649473	0.85[ASN][1000 genomes]
rs35351013	0.93[ASN][1000 genomes]
rs35468353	0.91[CEU][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35675346	1.00[JPT][hapmap]
rs35713203	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35961830	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4468641	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4527034	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs4889525	0.89[JPT][hapmap]
rs4889526	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4889530	0.87[ASN][1000 genomes]
rs4889599	0.87[CEU][hapmap];0.89[JPT][hapmap]
rs4889603	0.89[JPT][hapmap]
rs4889604	0.83[CEU][hapmap];0.89[JPT][hapmap]
rs4889606	0.89[JPT][hapmap]
rs4889609	0.91[CEU][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4889619	0.84[ASN][1000 genomes]
rs4889620	0.95[ASN][1000 genomes]
rs4889623	0.82[CHB][hapmap]
rs4889651	0.88[JPT][hapmap]
rs4889653	0.88[JPT][hapmap]
rs55766044	0.95[ASN][1000 genomes]
rs55979739	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56284083	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56314408	0.95[ASN][1000 genomes]
rs56813533	0.93[ASN][1000 genomes]
rs57434408	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57576577	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs58726213	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs59061704	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs59735493	0.95[ASN][1000 genomes]
rs60996860	0.91[ASN][1000 genomes]
rs61162043	1.00[ASN][1000 genomes]
rs61320757	0.95[ASN][1000 genomes]
rs6565217	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6950	0.87[CEU][hapmap];0.89[JPT][hapmap]
rs7184567	0.92[CEU][hapmap]
rs7187995	0.93[ASN][1000 genomes]
rs7190802	0.82[CHB][hapmap]
rs7196161	1.00[ASN][1000 genomes]
rs7196726	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7197717	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7199949	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7200879	1.00[JPT][hapmap]
rs7203999	0.87[CEU][hapmap];0.89[JPT][hapmap]
rs7204459	0.83[CEU][hapmap];0.89[JPT][hapmap]
rs7206511	0.89[JPT][hapmap]
rs7294	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs729482	0.87[CEU][hapmap];1.00[JPT][hapmap]
rs732172	0.91[CEU][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs732173	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73530203	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs749670	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs749671	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs749767	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7500176	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs750952	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8046707	0.89[JPT][hapmap]
rs8047803	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8050588	0.89[JPT][hapmap]
rs8050894	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs8056842	0.92[CEU][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8060857	0.83[CEU][hapmap];0.89[JPT][hapmap]
rs8061047	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8062719	0.87[CEU][hapmap];0.89[JPT][hapmap]
rs881929	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs889548	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs889555	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs897986	0.87[CEU][hapmap];0.89[JPT][hapmap]
rs9673641	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9923231	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9925964	0.95[ASN][1000 genomes]
rs9926533	0.89[JPT][hapmap]
rs9927295	0.82[YRI][hapmap]
rs9929899	0.86[ASN][1000 genomes]
rs9933843	0.88[JPT][hapmap]
rs9934438	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9936329	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs9938550	0.87[CEU][hapmap]
rs9939417	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs9939558	0.89[ASN][1000 genomes]
rs9972727	0.95[ASN][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	nsv1062456	chr16:30442166-31253997	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic 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	437 gene(s)	inside rSNPs	diseases
2	nsv542898	chr16:30442166-31253997	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
3	nsv905729	chr16:30642867-31247924	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	387 gene(s)	inside rSNPs	diseases
4	nsv431451	chr16:30682399-31340999	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers 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	350 gene(s)	inside rSNPs	diseases
5	nsv905734	chr16:30877544-31191482	Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
6	nsv905735	chr16:30890538-31247924	Strong transcription Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers 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	264 gene(s)	inside rSNPs	diseases
7	nsv457483	chr16:30903679-31191482	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
8	nsv571820	chr16:30903679-31191482	Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
9	esv1797877	chr16:30948643-31188432	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS 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 miRNA target site	114 gene(s)	inside rSNPs	diseases
10	nsv833193	chr16:30960796-31133604	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
11	nsv905740	chr16:31066249-31232437	Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	202 gene(s)	inside rSNPs	diseases
12	nsv905741	chr16:31066249-31247924	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription 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 target site	202 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs3751855	HSD3B7	cis	Skin Sun Exposed Lower leg	GTEx
rs3751855	STX4	Cis_1M	lymphoblastoid	RTeQTL
rs3751855	STX1B	cis	Thyroid	GTEx
rs3751855	HSD3B7	cis	Esophagus Mucosa	GTEx
rs3751855	RP11-196G11.2	cis	Esophagus Muscularis	GTEx
rs3751855	KAT8	cis	Artery Tibial	GTEx
rs3751855	MYST1	Cis_1M	lymphoblastoid	RTeQTL
rs3751855	HSD3B7	cis	Muscle Skeletal	GTEx
rs3751855	KAT8	cis	Skin Sun Exposed Lower leg	GTEx
rs3751855	RP11-196G11.2	cis	Muscle Skeletal	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31086400-31092400	Weak transcription	Small Intestine	intestine
2	chr16:31086400-31104400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr16:31086600-31104200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr16:31086600-31105200	Weak transcription	Right Atrium	heart
5	chr16:31086800-31093000	Weak transcription	Fetal Heart	heart
6	chr16:31087200-31092800	Strong transcription	Brain Substantia Nigra	brain
7	chr16:31087200-31093000	Strong transcription	Cortex derived primary cultured neurospheres	brain
8	chr16:31087200-31093200	Strong transcription	Stomach Smooth Muscle	stomach
9	chr16:31087200-31093400	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr16:31087200-31095800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr16:31087200-31097000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr16:31087200-31102000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr16:31087200-31103800	Strong transcription	NHLF	lung
14	chr16:31087200-31104200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr16:31087400-31092400	Strong transcription	Fetal Brain Female	brain
16	chr16:31087400-31092600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr16:31087400-31093000	Strong transcription	Brain Anterior Caudate	brain
18	chr16:31087400-31093000	Strong transcription	Brain Cingulate Gyrus	brain
19	chr16:31087400-31093000	Strong transcription	Brain Hippocampus Middle	brain
20	chr16:31087400-31093200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr16:31087400-31093200	Weak transcription	Stomach Mucosa	stomach
22	chr16:31087400-31093400	Strong transcription	Duodenum Mucosa	Duodenum
23	chr16:31087400-31095400	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr16:31087400-31095600	Strong transcription	Osteobl	bone
25	chr16:31087400-31096000	Strong transcription	HUES64 Cell Line	embryonic stem cell
26	chr16:31087400-31099200	Strong transcription	HepG2	liver
27	chr16:31087400-31101800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr16:31087400-31102800	Strong transcription	Thymus	Thymus
29	chr16:31087400-31103000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr16:31087400-31104400	Strong transcription	Primary T cells from cord blood	blood
31	chr16:31087400-31104400	Strong transcription	Fetal Intestine Small	intestine
32	chr16:31087600-31092000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr16:31087600-31092600	Strong transcription	Primary T helper cells PMA-I stimulated	--
34	chr16:31087600-31092600	Strong transcription	Rectal Smooth Muscle	rectum
35	chr16:31087600-31092800	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr16:31087600-31093000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr16:31087600-31093000	Strong transcription	Primary T helper cells fromperipheralblood	blood
38	chr16:31087600-31093000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr16:31087600-31093000	Strong transcription	Adipose Nuclei	Adipose
40	chr16:31087600-31093000	Strong transcription	Brain Angular Gyrus	brain
41	chr16:31087600-31093000	Strong transcription	Skeletal Muscle Male	skeletal muscle
42	chr16:31087600-31093400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
43	chr16:31087600-31093400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr16:31087600-31093400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr16:31087600-31093600	Strong transcription	H1 Cell Line	embryonic stem cell
46	chr16:31087600-31093600	Strong transcription	H9 Cell Line	embryonic stem cell
47	chr16:31087600-31093800	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr16:31087600-31094000	Genic enhancers	Pancreas	Pancrea
49	chr16:31087600-31094400	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr16:31087600-31094400	Strong transcription	Colonic Mucosa	Colon

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