Variant report

Variant	rs6426218
Chromosome Location	chr1:247259571-247259572
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:247241674..247243620-chr1:247259249..247261980,3	MCF-7	breast:
2	chr1:247253924..247257124-chr1:247257562..247261761,7	K562	blood:
3	chr1:247258817..247262425-chr1:247262948..247268807,7	MCF-7	breast:
4	chr1:247241429..247243620-chr1:247259025..247262045,3	K562	blood:
5	chr1:247258996..247260930-chr1:247274650..247277105,3	MCF-7	breast:
6	chr1:247256992..247261249-chr1:247272069..247275489,5	K562	blood:
7	chr1:247252127..247257268-chr1:247258904..247262111,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000221953	Chromatin interaction
ENSG00000135747	Chromatin interaction
ENSG00000188295	Chromatin interaction

Extended variants
information (count: 138 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:112)

rs_ID	r²[population]
rs1007457	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs10493861	0.90[CHB][hapmap]
rs10754536	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10802463	0.88[ASN][1000 genomes]
rs10802466	1.00[CHB][hapmap];0.81[CHD][hapmap];0.94[ASN][1000 genomes]
rs10802468	0.94[ASN][1000 genomes]
rs10802469	0.94[ASN][1000 genomes]
rs10924907	1.00[CHB][hapmap];0.90[JPT][hapmap];0.94[ASN][1000 genomes]
rs10924909	0.98[ASN][1000 genomes]
rs10924910	0.89[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10924912	0.92[ASN][1000 genomes]
rs10924914	0.94[ASN][1000 genomes]
rs10924915	0.92[ASN][1000 genomes]
rs10924917	0.92[ASN][1000 genomes]
rs10924919	0.92[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.84[GIH][hapmap];0.90[JPT][hapmap];0.92[ASN][1000 genomes]
rs11801681	0.80[ASN][1000 genomes]
rs12080836	0.92[ASN][1000 genomes]
rs12084753	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12093759	0.90[CHB][hapmap]
rs12094740	0.98[ASN][1000 genomes]
rs12119007	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs12119918	0.94[ASN][1000 genomes]
rs12121363	0.80[ASN][1000 genomes]
rs12122715	0.85[ASN][1000 genomes]
rs12127349	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs12128943	0.80[ASN][1000 genomes]
rs12129591	0.88[ASN][1000 genomes]
rs12131094	0.81[ASN][1000 genomes]
rs12133296	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs12133763	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap]
rs12138526	0.92[ASN][1000 genomes]
rs12138686	0.91[ASN][1000 genomes]
rs12140839	0.83[ASN][1000 genomes]
rs12141797	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12141826	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs12142274	0.86[ASN][1000 genomes]
rs12144733	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12144854	0.80[ASN][1000 genomes]
rs12691533	0.97[ASN][1000 genomes]
rs12723583	0.88[ASN][1000 genomes]
rs12740588	0.84[ASN][1000 genomes]
rs12751386	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs13376442	0.98[ASN][1000 genomes]
rs1552988	0.98[ASN][1000 genomes]
rs166643	0.84[ASN][1000 genomes]
rs1874407	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs192432	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs2055190	0.97[ASN][1000 genomes]
rs2055193	0.83[ASN][1000 genomes]
rs2172795	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs2270616	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2379192	0.90[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2379193	0.98[ASN][1000 genomes]
rs2642962	0.84[ASN][1000 genomes]
rs273378	0.85[ASN][1000 genomes]
rs2818880	0.84[ASN][1000 genomes]
rs2890101	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2890102	0.98[ASN][1000 genomes]
rs2890103	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2890104	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2890105	0.98[ASN][1000 genomes]
rs2890106	0.98[ASN][1000 genomes]
rs34060714	0.83[ASN][1000 genomes]
rs34225777	0.83[ASN][1000 genomes]
rs34273666	0.98[ASN][1000 genomes]
rs34350972	0.98[ASN][1000 genomes]
rs34764574	0.80[ASN][1000 genomes]
rs34870081	0.81[ASN][1000 genomes]
rs34919391	0.86[ASN][1000 genomes]
rs35314391	0.98[ASN][1000 genomes]
rs35452630	0.98[ASN][1000 genomes]
rs35511369	0.98[ASN][1000 genomes]
rs3736325	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3806269	1.00[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs3844079	0.90[CHB][hapmap]
rs3844080	0.90[CHB][hapmap]
rs3892246	0.98[ASN][1000 genomes]
rs3892516	0.98[ASN][1000 genomes]
rs41305955	0.95[ASN][1000 genomes]
rs4622098	0.80[ASN][1000 genomes]
rs4925692	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs4925702	0.80[ASN][1000 genomes]
rs4925704	0.80[ASN][1000 genomes]
rs55649449	0.86[ASN][1000 genomes]
rs57003817	0.98[ASN][1000 genomes]
rs60293371	0.98[ASN][1000 genomes]
rs60677310	0.98[ASN][1000 genomes]
rs60794525	0.98[ASN][1000 genomes]
rs6426209	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs6426217	0.92[ASN][1000 genomes]
rs6426220	0.90[CHB][hapmap];0.95[CHD][hapmap];0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs6658298	0.97[ASN][1000 genomes]
rs6659256	0.98[ASN][1000 genomes]
rs6664157	0.94[ASN][1000 genomes]
rs6669242	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.97[TSI][hapmap];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6675536	0.86[ASW][hapmap];0.90[CHB][hapmap]
rs6676355	0.82[ASN][1000 genomes]
rs6677000	0.86[ASN][1000 genomes]
rs6680033	0.81[ASN][1000 genomes]
rs6681227	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6685921	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6693464	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs6695894	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs6699898	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6702419	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7412787	0.97[ASN][1000 genomes]
rs7512931	0.80[ASN][1000 genomes]
rs7518407	0.86[ASN][1000 genomes]
rs7521596	0.90[CHB][hapmap]
rs7528817	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs7549674	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9793102	0.90[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006271	chr1:246832606-247276182	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv535416	chr1:246832606-247276182	Strong transcription ZNF genes & repeats Active TSS Enhancers Weak transcription 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 miRNA target site	52 gene(s)	inside rSNPs	diseases
3	nsv873424	chr1:246991094-247366380	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv1005208	chr1:247037441-247597975	Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
5	nsv535417	chr1:247094131-247409000	ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers 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 miRNA	47 gene(s)	inside rSNPs	diseases
6	nsv1005639	chr1:247094161-247401380	ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
7	nsv535418	chr1:247094161-247401380	Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
8	nsv999879	chr1:247112207-247276918	Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
9	nsv916236	chr1:247124353-247409065	Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
10	nsv948419	chr1:247130577-247400404	ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
11	nsv1012616	chr1:247173851-247365588	Active TSS Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
12	nsv535420	chr1:247173851-247365588	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
13	nsv1002438	chr1:247173851-247401380	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	30 gene(s)	inside rSNPs	diseases
14	nsv999352	chr1:247180668-247307074	Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
15	nsv535421	chr1:247180668-247307074	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
16	nsv997687	chr1:247180668-247348847	Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
17	nsv535422	chr1:247180668-247348847	ZNF genes & repeats Genic enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
18	nsv427974	chr1:247184802-247352964	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
19	esv3336179	chr1:247195262-247373269	Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
20	nsv533111	chr1:247200511-247264759	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
21	nsv1014012	chr1:247207932-247289138	Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
22	nsv873428	chr1:247226986-247346189	Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
23	nsv873429	chr1:247230809-247288469	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
24	nsv549547	chr1:247233156-247281769	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
25	nsv873430	chr1:247233156-247291400	ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
26	nsv873431	chr1:247242836-247297502	Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs6426218	ZNF238	cis	cerebellum	SCAN
rs6426218	ZNF669	cis	cerebellum	SCAN
rs6426218	ZNF124	cis	multi-tissue	Pritchard
rs6426218	ZNF670	cis	parietal	SCAN
rs6426218	MKNK2	trans	parietal	SCAN
rs6426218	ZNF669	cis	parietal	SCAN
rs6426218	ZNF670	cis	cerebellum	SCAN
rs6426218	ZNF124	cis	lymphoblastoid	seeQTL
rs6426218	LOC149134	cis	cerebellum	SCAN
rs6426218	ZNF124	cis	cerebellum	SCAN
rs6426218	ZNF669	cis	Muscle Skeletal	GTEx

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:247253200-247260400	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr1:247253200-247263800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:247253400-247260600	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr1:247253600-247260000	Weak transcription	Right Ventricle	heart
5	chr1:247253600-247260200	Weak transcription	Fetal Muscle Trunk	muscle
6	chr1:247253600-247263000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr1:247254000-247262800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:247254000-247263600	Weak transcription	Placenta	Placenta
9	chr1:247254200-247259600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr1:247254200-247260200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr1:247254200-247260200	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr1:247254200-247262000	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr1:247254200-247266600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:247254400-247260200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr1:247254400-247260600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr1:247255200-247260200	Weak transcription	Dnd41	blood
17	chr1:247255800-247260200	Weak transcription	Ovary	ovary
18	chr1:247257400-247260200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr1:247257600-247260200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr1:247257800-247260400	Weak transcription	Brain Anterior Caudate	brain
21	chr1:247257800-247260600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr1:247258000-247259800	Weak transcription	Brain Hippocampus Middle	brain
23	chr1:247258000-247263600	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr1:247258400-247260200	Weak transcription	Brain Angular Gyrus	brain
25	chr1:247258600-247260400	Weak transcription	Colon Smooth Muscle	Colon
26	chr1:247258600-247261400	ZNF genes & repeats	Primary B cells from cord blood	blood
27	chr1:247258600-247263600	Strong transcription	Brain Germinal Matrix	brain
28	chr1:247258800-247260200	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr1:247259000-247260600	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr1:247259000-247263600	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr1:247259000-247263600	Weak transcription	Fetal Heart	heart
32	chr1:247259200-247261000	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr1:247259200-247261000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr1:247259200-247261200	ZNF genes & repeats	Fetal Brain Female	brain
35	chr1:247259200-247262600	ZNF genes & repeats	K562	blood
36	chr1:247259400-247260200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr1:247259400-247261200	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr1:247259400-247261400	Strong transcription	Stomach Smooth Muscle	stomach
39	chr1:247259400-247266000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr1:247259400-247266000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain

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