Variant report

Variant	rs17006682
Chromosome Location	chr3:20201429-20201430
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:20195965..20199003-chr3:20200424..20204373,5	K562	blood:
2	chr3:20200366..20203372-chr3:20209857..20212107,3	K562	blood:
3	chr3:20199507..20201505-chr3:20225585..20228159,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000129810	Chromatin interaction

Extended variants
information (count: 119 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs11128941	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11128942	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1122135	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12486706	0.92[EUR][1000 genomes]
rs12637234	1.00[CEU][hapmap];0.90[GIH][hapmap];0.91[MEX][hapmap];0.84[TSI][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12639214	0.81[AMR][1000 genomes]
rs1567200	0.90[EUR][1000 genomes]
rs17006721	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17006733	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17006739	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17797971	0.89[CEU][hapmap]
rs1828079	0.87[CHB][hapmap];0.84[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs2068477	0.80[CEU][hapmap]
rs2292228	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3804567	0.81[AMR][1000 genomes]
rs3804568	1.00[CEU][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3804570	0.81[AMR][1000 genomes]
rs3804572	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3811674	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4076369	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs41276509	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4132121	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4308300	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4858157	1.00[CEU][hapmap];0.97[GIH][hapmap];0.91[MEX][hapmap];0.92[TSI][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4858159	0.90[EUR][1000 genomes]
rs4858160	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4858770	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4858775	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4858776	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4858777	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs57204823	0.92[EUR][1000 genomes]
rs58206832	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs58371809	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs58409904	0.90[EUR][1000 genomes]
rs58613937	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs59189930	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs59471185	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs59527607	0.85[ASN][1000 genomes]
rs60612263	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61206920	0.89[EUR][1000 genomes]
rs61207556	0.92[EUR][1000 genomes]
rs61729306	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62241665	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62241671	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62241672	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62241673	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62241699	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62241703	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62241706	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62241707	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62241708	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62241714	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62241752	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62241753	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62241756	0.81[EUR][1000 genomes]
rs62243138	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62243461	0.84[EUR][1000 genomes]
rs62243480	0.88[EUR][1000 genomes]
rs62243482	0.86[EUR][1000 genomes]
rs62243502	0.86[EUR][1000 genomes]
rs62243503	0.85[EUR][1000 genomes]
rs6550401	0.85[CEU][hapmap]
rs6550413	1.00[CEU][hapmap];0.91[CHB][hapmap];0.89[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6550419	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6550460	0.84[EUR][1000 genomes]
rs66968685	0.90[EUR][1000 genomes]
rs67253443	0.90[EUR][1000 genomes]
rs6761987	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6767445	0.86[EUR][1000 genomes]
rs6770526	0.90[EUR][1000 genomes]
rs6774000	0.85[CEU][hapmap];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6774152	0.85[EUR][1000 genomes]
rs6776870	0.83[CEU][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6777193	0.86[EUR][1000 genomes]
rs6778969	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6782533	0.92[EUR][1000 genomes]
rs67949984	0.90[EUR][1000 genomes]
rs68098782	0.88[EUR][1000 genomes]
rs7620481	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7622992	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7623136	0.86[EUR][1000 genomes]
rs7629055	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7640134	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs906468	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs937886	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9832994	0.84[EUR][1000 genomes]
rs9838186	0.85[EUR][1000 genomes]
rs9838851	0.90[EUR][1000 genomes]
rs9845960	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1833006	chr3:19562271-20389045	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv1010613	chr3:19942032-20461486	Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	esv1826830	chr3:19982972-20632072	Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	esv1829542	chr3:20009231-20384627	Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv834627	chr3:20068115-20227975	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv433359	chr3:20090908-20587572	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv470450	chr3:20096735-20389045	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
8	nsv1001006	chr3:20110743-20752628	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
9	nsv536512	chr3:20110743-20752628	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
10	esv1829018	chr3:20116077-20596244	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
11	esv1827700	chr3:20119716-20489086	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
12	esv1830036	chr3:20121828-20278275	Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
13	esv1830599	chr3:20121828-20375643	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
14	esv1828816	chr3:20136508-20389045	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
15	esv3394910	chr3:20150394-20203576	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
16	esv3334928	chr3:20150414-20203546	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
17	esv1832674	chr3:20152772-20605302	Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
18	esv1831853	chr3:20157077-20615273	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
19	esv1833208	chr3:20157077-20638228	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
20	esv2422249	chr3:20163608-20626956	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
21	esv1826144	chr3:20164282-20638228	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
22	nsv1013532	chr3:20172889-20305612	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
23	nsv536513	chr3:20172889-20305612	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
24	esv1831289	chr3:20191506-20617984	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
25	esv1829973	chr3:20192578-20375260	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
26	esv1829847	chr3:20196923-20638228	Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
27	nsv876597	chr3:20197364-20242143	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
28	esv2637952	chr3:20200095-20201582	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
29	esv1829457	chr3:20200232-20375260	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
30	esv1830113	chr3:20200232-20430932	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs17006682	SGOL1	cis	lymphoblastoid	seeQTL
rs17006682	KAT2B	cis	parietal	SCAN

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20141200-20222400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:20164400-20204400	Weak transcription	Small Intestine	intestine
3	chr3:20164800-20211400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr3:20167800-20226000	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr3:20169800-20201600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr3:20169800-20202000	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr3:20184600-20220200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr3:20188400-20204800	Weak transcription	Fetal Brain Female	brain
9	chr3:20188400-20212400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr3:20189800-20201600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr3:20190200-20201800	Weak transcription	Fetal Intestine Large	intestine
12	chr3:20190400-20202400	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr3:20190600-20220200	Weak transcription	Fetal Muscle Leg	muscle
14	chr3:20191800-20201800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr3:20191800-20201800	Weak transcription	Adipose Nuclei	Adipose
16	chr3:20191800-20202400	Weak transcription	Duodenum Mucosa	Duodenum
17	chr3:20191800-20202600	Weak transcription	Brain Cingulate Gyrus	brain
18	chr3:20192400-20201800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr3:20192800-20220600	Weak transcription	Fetal Lung	lung
20	chr3:20193000-20201800	Weak transcription	Colon Smooth Muscle	Colon
21	chr3:20193200-20204000	Strong transcription	Fetal Thymus	thymus
22	chr3:20193800-20226600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
23	chr3:20194000-20220400	Weak transcription	NH-A	brain
24	chr3:20194200-20201600	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr3:20194200-20205400	Strong transcription	Dnd41	blood
26	chr3:20194800-20215200	Weak transcription	HepG2	liver
27	chr3:20195000-20212400	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr3:20195000-20226000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr3:20195200-20201600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr3:20195200-20203800	Strong transcription	HUES6 Cell Line	embryonic stem cell
31	chr3:20195200-20221800	Weak transcription	NHEK	skin
32	chr3:20195400-20226000	Weak transcription	NHDF-Ad	bronchial
33	chr3:20195400-20226200	Weak transcription	NHLF	lung
34	chr3:20195600-20212000	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr3:20196400-20204000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr3:20196400-20225600	Strong transcription	HUES64 Cell Line	embryonic stem cell
37	chr3:20196800-20201800	Weak transcription	Primary hematopoietic stem cells	blood
38	chr3:20196800-20221600	Weak transcription	Fetal Intestine Small	intestine
39	chr3:20197000-20226200	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr3:20197000-20226800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr3:20197400-20227000	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr3:20197600-20226800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr3:20198000-20201600	Weak transcription	Primary B cells from cord blood	blood
44	chr3:20198000-20203600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr3:20198200-20219800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr3:20198400-20202400	Weak transcription	HUVEC	blood vessel
47	chr3:20198400-20204200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr3:20198600-20220200	Weak transcription	Thymus	Thymus
49	chr3:20198800-20201800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr3:20199000-20203400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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