Variant report

Variant	rs13072608
Chromosome Location	chr3:195800267-195800268
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:280)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr3:195799871-195801039	K562	blood:	n/a	n/a
2	RUNX3	chr3:195800042-195800556	GM12878	blood:	n/a	n/a
3	RAD21	chr3:195799961-195800710	HCT-116	colon:	n/a	n/a
4	CTCF	chr3:195800145-195800410	ProgFib	skin:	n/a	n/a
5	RAD21	chr3:195800038-195800542	HCT-116	colon:	n/a	n/a
6	MAX	chr3:195800097-195800460	K562	blood:	n/a	n/a
7	CTCF	chr3:195800240-195800390	GM12872	blood:	n/a	n/a
8	RAD21	chr3:195800045-195800522	HepG2	liver:	n/a	n/a
9	CTCF	chr3:195800200-195800350	HA-sp	spinal cord:	n/a	n/a
10	CTCF	chr3:195800260-195800410	GM12801	blood:	n/a	n/a
11	CTCF	chr3:195800160-195800310	GM12865	blood:	n/a	n/a
12	CTCF	chr3:195800240-195800390	BE2_C	brain:	n/a	n/a
13	CTCF	chr3:195800200-195800350	AoAF	blood vessel:	n/a	n/a
14	CTCF	chr3:195799976-195800559	MCF-7	breast:	n/a	n/a
15	SMC3	chr3:195800098-195800532	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr3:195800240-195800390	GM12871	blood:	n/a	n/a
17	CTCF	chr3:195800220-195800370	AG10803	skin:	n/a	n/a
18	CTCF	chr3:195800104-195800488	K562	blood:	n/a	n/a
19	CTCF	chr3:195800193-195800409	GM20000	blood:	n/a	n/a
20	GTF2F1	chr3:195800145-195800452	H1-hESC	embryonic stem cell:	n/a	n/a
21	MAX	chr3:195800128-195800521	NB4	blood:	n/a	n/a
22	MAX	chr3:195800155-195800455	H1-hESC	embryonic stem cell:	n/a	n/a
23	RAD21	chr3:195800126-195800519	GM12878	blood:	n/a	n/a
24	CTCF	chr3:195800120-195800270	A549	lung:	n/a	n/a
25	CTCF	chr3:195800086-195800515	GM12878	blood:	n/a	n/a
26	TBL1XR1	chr3:195800180-195800531	K562	blood:	n/a	n/a
27	CTCF	chr3:195800105-195800497	IMR90	lung:	n/a	n/a
28	POLR2A	chr3:195800023-195800886	GM12892	blood:	n/a	n/a
29	CTCF	chr3:195800138-195800415	MCF-7	breast:	n/a	n/a
30	RAD21	chr3:195800107-195800565	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr3:195800240-195800390	GM06990	blood:	n/a	n/a
32	USF2	chr3:195800137-195800525	Hela-S3	cervix:	n/a	n/a
33	RAD21	chr3:195800024-195800625	MCF-7	breast:	n/a	n/a
34	CTCF	chr3:195800260-195800410	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:195800160-195800310	HAc	cerebellar:	n/a	n/a
36	CTCF	chr3:195800115-195800416	SK-N-SH_RA	brain:	n/a	n/a
37	ZNF143	chr3:195800152-195800450	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr3:195800180-195800330	GM12866	blood:	n/a	n/a
39	CTCF	chr3:195800200-195800350	HMEC	breast:	n/a	n/a
40	CTCF	chr3:195800180-195800330	HFF-Myc	foreskin:	n/a	n/a
41	JUND	chr3:195800190-195800432	K562	blood:	n/a	n/a
42	CTCF	chr3:195800220-195800370	HPF	lung:	n/a	n/a
43	CTCF	chr3:195800160-195800310	NHEK	skin:	n/a	n/a
44	CTCF	chr3:195800189-195800384	GM13976	blood:	n/a	n/a
45	RAD21	chr3:195800121-195800541	GM12878	blood:	n/a	n/a
46	TBL1XR1	chr3:195800181-195800361	K562	blood:	n/a	n/a
47	CTCF	chr3:195800124-195800401	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr3:195800089-195800498	ECC-1	luminal epithelium:	n/a	n/a
49	CTCF	chr3:195800149-195800419	GM19239	blood:	n/a	n/a
50	CTCF	chr3:195800220-195800370	GM12864	blood:	n/a	n/a

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:195796379..195810322-chr3:195910077..195926320,43	MCF-7	breast:
2	chr3:195785669..195789364-chr3:195799145..195802240,3	MCF-7	breast:
3	chr3:195799991..195800538-chr3:195921654..195922302,2	MCF-7	breast:
4	chr3:195799737..195801864-chr3:196158753..196160544,2	MCF-7	breast:
5	chr3:195793504..195812987-chr3:195901613..195938073,113	K562	blood:
6	chr3:195798458..195803942-chr3:195919017..195926093,8	MCF-7	breast:
7	chr3:195799879..195800777-chr3:195923152..195924143,8	K562	blood:
8	chr3:195799820..195800471-chr3:195922951..195923671,2	MCF-7	breast:
9	chr3:195790325..195795087-chr3:195795509..195801809,7	MCF-7	breast:
10	chr3:195793504..195812415-chr3:195915832..195927942,46	K562	blood:

No data

Variant related genes	Relation type
TFRC	TF binding region
ENSG00000163958	Chromatin interaction
ENSG00000222335	Chromatin interaction
ENSG00000163960	Chromatin interaction
ENSG00000072274	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11185506	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11718657	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2239640	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2239641	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2284889	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2284890	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2300773	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2300774	0.91[CEU][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2300775	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2300777	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2300778	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2300780	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2638904	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34221479	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35587059	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3761717	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3789135	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs3804139	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3804140	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3817672	1.00[CHB][hapmap];0.86[JPT][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3933	0.82[CEU][hapmap]
rs406271	0.82[CEU][hapmap]
rs41300431	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs557527	0.89[CEU][hapmap]
rs9846149	0.96[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9852239	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9852883	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9858727	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9859260	0.96[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];0.97[ASN][1000 genomes]
rs9859401	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9863872	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9877119	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9990392	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2759213	chr3:195102787-196071593	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats 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	144 gene(s)	inside rSNPs	diseases
2	nsv428102	chr3:195201080-195829426	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	nsv428430	chr3:195201080-195829426	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
4	esv2757913	chr3:195379484-196071593	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
5	nsv1010395	chr3:195641908-195848264	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
6	nsv532213	chr3:195643944-196063636	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
7	esv1820982	chr3:195651349-195835519	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
8	nsv997797	chr3:195658360-196212958	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
9	nsv878170	chr3:195677895-195871388	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
10	nsv878171	chr3:195677895-195959924	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
11	nsv1008512	chr3:195709662-195974936	Strong transcription Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
12	nsv1002584	chr3:195734933-195910772	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer 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 target site	51 gene(s)	inside rSNPs	diseases
13	nsv432543	chr3:195746690-196015690	Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription 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 miRNA target site	69 gene(s)	inside rSNPs	diseases
14	nsv878172	chr3:195751853-195831098	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
15	nsv532214	chr3:195762648-195916068	Weak transcription Strong transcription Active TSS Enhancers Flanking 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 target site	50 gene(s)	inside rSNPs	diseases
16	nsv1002065	chr3:195769609-195877692	Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
17	nsv1009105	chr3:195769609-195984388	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
18	nsv524410	chr3:195776240-195816195	Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
19	nsv461130	chr3:195776240-195907653	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
20	nsv593069	chr3:195776240-195907653	Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
21	nsv1005558	chr3:195789462-195919077	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
22	nsv536890	chr3:195789462-195919077	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195771400-195804000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
2	chr3:195773000-195802000	Strong transcription	Dnd41	blood
3	chr3:195773200-195805200	Strong transcription	Fetal Thymus	thymus
4	chr3:195773400-195800400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr3:195774200-195803800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr3:195774200-195804800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr3:195774400-195803800	Strong transcription	Duodenum Mucosa	Duodenum
8	chr3:195774600-195803800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr3:195774600-195805400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr3:195774800-195803000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr3:195774800-195803400	Strong transcription	Left Ventricle	heart
12	chr3:195775000-195803200	Strong transcription	Duodenum Smooth Muscle	Duodenum
13	chr3:195775000-195806600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr3:195775200-195802800	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr3:195775200-195804000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr3:195775200-195804400	Strong transcription	Sigmoid Colon	Sigmoid Colon
17	chr3:195775400-195800400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr3:195775400-195802600	Strong transcription	Primary T cells from cord blood	blood
19	chr3:195775400-195802800	Strong transcription	Fetal Brain Female	brain
20	chr3:195775400-195803400	Strong transcription	Fetal Muscle Trunk	muscle
21	chr3:195775400-195803800	Strong transcription	Primary hematopoietic stem cells	blood
22	chr3:195775400-195804000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr3:195775400-195804000	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr3:195775600-195802400	Strong transcription	NH-A	brain
25	chr3:195775600-195802800	Strong transcription	Skeletal Muscle Male	skeletal muscle
26	chr3:195775600-195803000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr3:195775600-195803400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr3:195775600-195804000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr3:195775800-195803200	Strong transcription	Fetal Muscle Leg	muscle
30	chr3:195775800-195803200	Strong transcription	Rectal Mucosa Donor 31	rectum
31	chr3:195775800-195804000	Strong transcription	Primary T cells fromperipheralblood	blood
32	chr3:195775800-195804000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr3:195776000-195803400	Strong transcription	HUVEC	blood vessel
34	chr3:195776400-195802800	Strong transcription	Stomach Smooth Muscle	stomach
35	chr3:195776400-195803000	Strong transcription	Brain Inferior Temporal Lobe	brain
36	chr3:195777000-195803400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr3:195777800-195804200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr3:195778400-195803400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr3:195778800-195803800	Strong transcription	Fetal Stomach	stomach
40	chr3:195780000-195803800	Strong transcription	Cortex derived primary cultured neurospheres	brain
41	chr3:195783000-195805800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr3:195783200-195802600	Strong transcription	Adipose Nuclei	Adipose
43	chr3:195783200-195803600	Strong transcription	Primary neutrophils fromperipheralblood	blood
44	chr3:195783400-195803800	Strong transcription	HepG2	liver
45	chr3:195783400-195804000	Strong transcription	Monocytes-CD14+_RO01746	blood
46	chr3:195783800-195804200	Strong transcription	Primary monocytes fromperipheralblood	blood
47	chr3:195784000-195802600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr3:195784800-195804200	Strong transcription	HMEC	breast
49	chr3:195785200-195807400	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr3:195785400-195802000	Strong transcription	Hela-S3	cervix

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