Variant report

Variant	rs11978101
Chromosome Location	chr7:4116665-4116666
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 160 )
Associated
traits (count: 9 )

rSNPs within LD-proxies of this variant (count:133)

rs_ID	r²[population]
rs1004043	0.88[CHB][hapmap];1.00[CHD][hapmap];0.88[ASN][1000 genomes]
rs10226642	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10229207	0.86[CHB][hapmap];0.93[CHD][hapmap];0.88[ASN][1000 genomes]
rs10230707	0.86[CHB][hapmap]
rs10231929	0.86[CHD][hapmap]
rs10234405	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs10235315	0.88[ASN][1000 genomes]
rs10236620	0.88[ASN][1000 genomes]
rs10237488	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs10237838	0.86[CHB][hapmap];0.93[CHD][hapmap];0.88[ASN][1000 genomes]
rs10237842	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs10237956	0.88[ASN][1000 genomes]
rs10242122	0.86[CHB][hapmap];1.00[CHD][hapmap]
rs10244597	0.86[CHB][hapmap];0.93[CHD][hapmap];0.88[ASN][1000 genomes]
rs10251829	0.94[ASN][1000 genomes]
rs10253393	0.86[CHB][hapmap];0.93[CHD][hapmap];0.88[ASN][1000 genomes]
rs10255116	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs10259751	0.86[CHB][hapmap];0.93[CHD][hapmap];0.88[ASN][1000 genomes]
rs10259896	0.86[CHB][hapmap];0.93[CHD][hapmap];0.88[ASN][1000 genomes]
rs10262417	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10263906	0.85[ASN][1000 genomes]
rs10265219	0.88[ASN][1000 genomes]
rs10265937	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs10266101	0.86[CHB][hapmap];0.86[CHD][hapmap];0.88[ASN][1000 genomes]
rs10270404	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10278187	1.00[CHB][hapmap];0.88[ASN][1000 genomes]
rs11975100	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs11975109	0.88[ASN][1000 genomes]
rs11976085	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11976431	0.86[CHB][hapmap];1.00[CHD][hapmap]
rs11979803	0.86[CHD][hapmap]
rs12155028	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs12155317	0.84[CHB][hapmap];0.88[ASN][1000 genomes]
rs12386617	0.86[CHB][hapmap];0.85[ASN][1000 genomes]
rs12701386	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12701396	0.86[CHB][hapmap]
rs12701401	0.86[CHD][hapmap]
rs13223359	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.89[TSI][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13226987	0.86[CHD][hapmap]
rs13229520	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13233532	0.86[CHD][hapmap]
rs13241881	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1443647	0.86[CHB][hapmap];0.93[CHD][hapmap];0.88[ASN][1000 genomes]
rs1562005	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs17134196	0.86[CHB][hapmap];0.93[CHD][hapmap];0.85[ASN][1000 genomes]
rs17134197	0.85[ASN][1000 genomes]
rs17134314	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1807027	0.94[ASN][1000 genomes]
rs2342489	0.85[CHB][hapmap];0.88[ASN][1000 genomes]
rs2342490	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs2342491	0.86[CHB][hapmap];0.93[CHD][hapmap];0.88[ASN][1000 genomes]
rs2342492	0.88[ASN][1000 genomes]
rs2342493	0.88[ASN][1000 genomes]
rs2342496	0.91[ASN][1000 genomes]
rs2342497	0.86[CHD][hapmap]
rs2342498	0.86[CHD][hapmap]
rs28634483	0.88[ASN][1000 genomes]
rs2880371	0.86[CHB][hapmap];0.93[CHD][hapmap];0.88[ASN][1000 genomes]
rs28828193	0.88[ASN][1000 genomes]
rs34176245	0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34241728	0.88[ASN][1000 genomes]
rs34656116	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34786362	0.88[ASN][1000 genomes]
rs4295561	0.86[CHB][hapmap];0.92[CHD][hapmap];0.88[ASN][1000 genomes]
rs4391327	0.85[CHB][hapmap];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4442012	0.86[CHD][hapmap]
rs4526263	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs55808604	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55961125	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56249161	0.88[EUR][1000 genomes]
rs56294271	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57367972	0.85[ASN][1000 genomes]
rs58608919	1.00[ASN][1000 genomes]
rs58704629	1.00[ASN][1000 genomes]
rs60977750	0.80[AFR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6462541	0.85[CHB][hapmap];0.88[ASN][1000 genomes]
rs6462542	0.88[ASN][1000 genomes]
rs6462543	0.88[ASN][1000 genomes]
rs6462545	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs6462546	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs6462548	0.88[ASN][1000 genomes]
rs6462549	0.85[CHB][hapmap];0.88[ASN][1000 genomes]
rs6462550	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs6462558	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs6462562	0.86[CHD][hapmap]
rs6462564	0.88[CHB][hapmap];0.91[ASN][1000 genomes]
rs6462570	0.86[CHD][hapmap]
rs6462575	1.00[ASN][1000 genomes]
rs6462576	0.85[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6462577	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs66731402	0.88[ASN][1000 genomes]
rs67819387	0.88[ASN][1000 genomes]
rs67820803	0.88[ASN][1000 genomes]
rs68189920	0.88[ASN][1000 genomes]
rs6946871	0.86[CHB][hapmap];0.93[CHD][hapmap];0.88[ASN][1000 genomes]
rs6950754	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs6953284	0.88[ASN][1000 genomes]
rs6953630	0.88[ASN][1000 genomes]
rs6954175	0.88[ASN][1000 genomes]
rs6958964	0.94[ASN][1000 genomes]
rs6971090	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6977489	0.88[ASN][1000 genomes]
rs71527466	0.85[ASN][1000 genomes]
rs7783519	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs7784928	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7789457	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7789676	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7790866	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs7790901	0.86[CHD][hapmap]
rs7790918	0.86[CHD][hapmap]
rs7791013	0.88[ASN][1000 genomes]
rs7791029	0.88[ASN][1000 genomes]
rs7791174	0.85[CHB][hapmap];0.88[ASN][1000 genomes]
rs7791801	0.88[ASN][1000 genomes]
rs7794939	0.86[CHD][hapmap]
rs7797081	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs7797437	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7801112	0.91[ASN][1000 genomes]
rs7801816	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs7801843	0.86[CHD][hapmap]
rs7801852	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7801978	1.00[ASN][1000 genomes]
rs7802118	0.86[CHD][hapmap]
rs7802663	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7803030	0.86[CHB][hapmap];0.93[CHD][hapmap];0.88[ASN][1000 genomes]
rs7803897	0.88[ASN][1000 genomes]
rs7805933	0.86[CHB][hapmap];0.88[ASN][1000 genomes]
rs7806125	1.00[ASN][1000 genomes]
rs7807206	1.00[ASN][1000 genomes]
rs7807325	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7807506	1.00[ASN][1000 genomes]
rs7809492	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[TSI][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7810949	0.86[CHB][hapmap];1.00[CHD][hapmap];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021650	chr7:3665232-4577439	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh 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
2	nsv1029406	chr7:3860894-4477095	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv538685	chr7:3860894-4477095	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1026410	chr7:3869104-4383606	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1025497	chr7:3905444-4176032	Enhancers Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv538686	chr7:3905444-4176032	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv464274	chr7:3955516-4613607	Weak transcription Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv464275	chr7:3955516-4613607	Enhancers Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv464276	chr7:3955516-4613607	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv464277	chr7:3955516-4613607	Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv464278	chr7:3955516-4613607	Strong transcription Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv605939	chr7:3955516-4613607	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv1019305	chr7:3991646-4276004	Enhancers Weak transcription Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv1033687	chr7:4006020-4267871	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv538688	chr7:4006020-4267871	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv917252	chr7:4017819-4374090	Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
17	nsv527624	chr7:4027536-4424054	Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
18	nsv1022794	chr7:4063874-4137968	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
19	nsv538689	chr7:4063874-4137968	Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
20	nsv869540	chr7:4063875-4302040	Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
21	nsv1028689	chr7:4078345-4166552	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
22	nsv538690	chr7:4078345-4166552	Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
23	nsv1018462	chr7:4097676-4173613	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
24	nsv1016507	chr7:4105420-4255439	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
25	nsv538691	chr7:4105420-4255439	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
26	esv2755976	chr7:4116507-4207997	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
27	nsv518299	chr7:4116665-4286597	Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:9)

SNP	Gene	Cis/trans	Tissue	Source
rs11978101	UNCX	cis	cerebellum	SCAN
rs11978101	SDK1	cis	brain	BrainEAC
rs11978101	SDK1	cis	frontal cortex	BrainEAC
rs11978101	SDK1	cis	temporal cortex	BrainEAC
rs11978101	SDK1	cis	cerebellar cortex	BrainEAC
rs11978101	SDK1	cis	occipital cortex	BrainEAC
rs11978101	SDK1	cis	intralobular white matter	BrainEAC
rs11978101	SDK1	cis	substantia nigra	BrainEAC
rs11978101	SDK1	cis	thalamus	BrainEAC

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4088800-4129400	Weak transcription	Right Ventricle	heart
2	chr7:4103000-4125600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:4105200-4117000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:4105200-4120200	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr7:4106600-4117000	Weak transcription	Fetal Brain Female	brain
6	chr7:4107800-4120200	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr7:4109200-4118200	Weak transcription	Stomach Smooth Muscle	stomach
8	chr7:4109600-4122000	Weak transcription	Esophagus	oesophagus
9	chr7:4110200-4118400	Weak transcription	Gastric	stomach
10	chr7:4110200-4129400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr7:4111400-4119600	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr7:4112400-4130200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr7:4112600-4119600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:4113000-4118000	Weak transcription	Fetal Muscle Trunk	muscle
15	chr7:4113800-4120800	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr7:4114200-4118600	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr7:4116200-4116800	ZNF genes & repeats	Spleen	Spleen
18	chr7:4116200-4117000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr7:4116200-4117200	Strong transcription	Fetal Intestine Small	intestine
20	chr7:4116200-4117200	Strong transcription	Pancreas	Pancrea
21	chr7:4116200-4117400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr7:4116200-4129200	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr7:4116400-4117000	Strong transcription	H9 Cell Line	embryonic stem cell
24	chr7:4116400-4117000	Strong transcription	Adipose Nuclei	Adipose
25	chr7:4116400-4117200	Strong transcription	Primary neutrophils fromperipheralblood	blood
26	chr7:4116400-4117600	Strong transcription	Fetal Lung	lung
27	chr7:4116400-4118000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr7:4116400-4118000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr7:4116400-4118000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr7:4116400-4118800	Strong transcription	Aorta	Aorta
31	chr7:4116600-4117000	Strong transcription	Fetal Stomach	stomach

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