Variant report

Variant	rs9380220
Chromosome Location	chr6:31146584-31146585
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:9 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr6:31146128-31146609	GM12878	blood:	n/a	n/a
2	RCOR1	chr6:31146561-31146837	K562	blood:	n/a	n/a
3	ELF1	chr6:31146512-31146777	K562	blood:	n/a	chr6:31146665-31146678
4	NFIC	chr6:31146141-31146652	GM12878	blood:	n/a	n/a
5	FOXM1	chr6:31146131-31146628	GM12878	blood:	n/a	n/a
6	RUNX3	chr6:31145936-31146633	GM12878	blood:	n/a	n/a
7	IKZF1	chr6:31146099-31146847	GM12878	blood:	n/a	chr6:31146567-31146579
8	ATF2	chr6:31146133-31146669	GM12878	blood:	n/a	n/a
9	MTA3	chr6:31145985-31146731	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31146583-31146633	ECC-1	luminal epithelium:	n/a
2	chr6:31146583-31146633	HMEC	breast:	n/a
3	chr6:31146583-31146633	HNPCEpiC	eye:	n/a
4	chr6:31146583-31146633	NHBE	bronchial:	n/a
5	chr6:31146583-31146633	HUVEC	blood vessel:	n/a
6	chr6:31146583-31146633	AG09319	gingival:	n/a
7	chr6:31146583-31146633	BE2_C	brain:	n/a
8	chr6:31146583-31146633	LNCaP	prostate:	n/a
9	chr6:31146583-31146633	MCF10A-Er-Src	breast:	n/a
10	chr6:31146583-31146633	AG04450	lung:	fetal
11	chr6:31146583-31146633	PrEC	prostate:	n/a
12	chr6:31146583-31146633	ProgFib	skin:	n/a
13	chr6:31146583-31146633	Caco-2	colon:	n/a
14	chr6:31146583-31146633	NT2-D1	testis:	n/a
15	chr6:31146583-31146633	Hela-S3	cervix:	n/a
16	chr6:31146583-31146633	ovcar-3	ovarian:	n/a
17	chr6:31146583-31146633	SK-N-MC	brain:	n/a
18	chr6:31146583-31146633	RPTEC	kidney:	n/a
19	chr6:31146583-31146633	GM12878	blood:	n/a
20	chr6:31146583-31146633	BJ	skin:	n/a
21	chr6:31146583-31146633	AoSMC	blood vessel:	n/a
22	chr6:31146583-31146633	HCF	heart:	n/a
23	chr6:31146583-31146633	HRPEpiC	eye:	n/a
24	chr6:31146583-31146633	HIPEpiC	eye:	n/a
25	chr6:31146583-31146633	HepG2	liver:	n/a
26	chr6:31146583-31146633	GM12892	blood:	n/a
27	chr6:31146583-31146633	GM12891	blood:	n/a
28	chr6:31146583-31146633	NH-A	brain:	n/a
29	chr6:31146583-31146633	SK-N-SH_RA	brain:	n/a
30	chr6:31146583-31146633	H1-hESC	embryonic stem cell:	embryo
31	chr6:31146583-31146633	GM06990	blood:	n/a
32	chr6:31146583-31146633	K562	blood:	n/a
33	chr6:31146583-31146633	HAEpiC	amniotic membrane:	n/a
34	chr6:31146583-31146633	HEEpiC	esophagus:	n/a
35	chr6:31146583-31146633	Jurkat	blood:	n/a
36	chr6:31146583-31146633	NB4	blood:	n/a
37	chr6:31146583-31146633	Hepatocyte	liver:	n/a
38	chr6:31146583-31146633	AG09309	skin:	n/a
39	chr6:31146583-31146633	A549	lung:	n/a
40	chr6:31146583-31146633	NHDF-neo	bronchial:	n/a
41	chr6:31146583-31146633	GM19239	blood:	n/a
42	chr6:31146583-31146633	PFSK-1	brain:	n/a
43	chr6:31146583-31146633	HPAEpiC	pulmonary alveolar:	n/a
44	chr6:31146583-31146633	CMK	blood:	n/a
45	chr6:31146583-31146633	U87	brain:	n/a
46	chr6:31146583-31146633	HL-60	blood:	n/a
47	chr6:31146583-31146633	HEK293	kidney:	embryo
48	chr6:31146583-31146633	HCPEpiC	choroid plexus:	n/a
49	chr6:31146583-31146633	SAEC	small airway:	n/a
50	chr6:31146583-31146633	IMR90	lung:	fetal

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:31136072..31138764-chr6:31142991..31146892,3	MCF-7	breast:
2	chr6:31121111..31123929-chr6:31146425..31148442,2	MCF-7	breast:

No data

Variant related genes	Relation type
PSORS1C3	TF binding region
PSORS1C3	CpG island
ENSG00000204536	Chromatin interaction
ENSG00000204531	Chromatin interaction

Extended variants
information (count: 100 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs1052989	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11381232	0.81[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs11507945	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11961945	0.87[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs11961983	0.90[AFR][1000 genomes]
rs11967629	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1265160	0.94[AFR][1000 genomes]
rs1265163	0.94[AFR][1000 genomes]
rs28360055	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28360056	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28360057	0.93[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs28360058	0.93[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs28360059	0.93[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs28360060	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28360061	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28360062	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28360063	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28360064	0.81[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs28360065	0.83[ASN][1000 genomes]
rs28360066	0.81[ASN][1000 genomes]
rs28360067	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28397268	0.89[ASN][1000 genomes]
rs28397269	0.83[AFR][1000 genomes]
rs28397270	0.91[ASN][1000 genomes]
rs28397271	0.91[ASN][1000 genomes]
rs28397273	0.89[ASN][1000 genomes]
rs28397274	0.87[ASN][1000 genomes]
rs28397276	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28397277	0.90[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs28397282	0.92[ASN][1000 genomes]
rs28397284	0.90[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs28397285	0.81[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs28397286	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28749548	0.96[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs28749549	0.93[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs28749550	0.93[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs28749551	0.90[AFR][1000 genomes]
rs34467061	0.92[ASN][1000 genomes]
rs4122189	0.81[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs4713441	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4713442	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6899874	0.81[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs6899875	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6901685	0.82[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs6921663	0.82[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs6922077	0.82[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs6922553	0.93[ASN][1000 genomes]
rs6922756	0.91[ASN][1000 genomes]
rs6922842	0.89[ASN][1000 genomes]
rs6922994	0.82[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs6927253	0.91[ASN][1000 genomes]
rs6936474	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6936597	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6941912	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7741829	0.85[ASN][1000 genomes]
rs7755702	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7772290	0.86[ASN][1000 genomes]
rs887464	0.85[ASN][1000 genomes]
rs915660	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9263852	0.82[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs9263869	0.81[ASN][1000 genomes]
rs9295957	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9295958	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9357109	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9357113	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9357115	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9366769	0.92[ASN][1000 genomes]
rs9368661	0.82[ASN][1000 genomes]
rs9368662	0.84[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs9368663	0.84[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9378115	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9380221	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9380222	0.92[ASN][1000 genomes]
rs9380223	0.82[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs9391712	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9391815	0.82[ASN][1000 genomes]
rs9391818	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9394042	0.81[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs9404983	0.92[ASN][1000 genomes]
rs9405052	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9468882	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3519970	chr6:30382942-31378788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
2	esv3519971	chr6:30382942-31378788	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
3	nsv601481	chr6:30422632-31284253	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1012 gene(s)	inside rSNPs	diseases
4	nsv1015372	chr6:30704734-31582152	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
5	nsv538173	chr6:30704734-31582152	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
6	nsv1029442	chr6:31006647-31449207	Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
7	nsv427750	chr6:31028290-31234581	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
8	nsv428140	chr6:31028290-31462106	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	89 gene(s)	inside rSNPs	diseases
9	esv2758042	chr6:31028290-31497106	Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	101 gene(s)	inside rSNPs	diseases
10	esv2759414	chr6:31028290-31542308	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	151 gene(s)	inside rSNPs	diseases
11	nsv1019637	chr6:31104401-31354706	Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
12	nsv1029569	chr6:31104401-31412740	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	68 gene(s)	inside rSNPs	diseases
13	nsv538174	chr6:31104401-31412740	Flanking Bivalent TSS/Enh Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	68 gene(s)	inside rSNPs	diseases
14	nsv1034391	chr6:31131121-31279595	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
15	nsv1025909	chr6:31131121-31354706	Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	51 gene(s)	inside rSNPs	diseases
16	nsv538175	chr6:31131121-31354706	Active TSS Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	51 gene(s)	inside rSNPs	diseases
17	nsv1015890	chr6:31131121-31449207	Enhancers Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
18	nsv538176	chr6:31131121-31449207	Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
19	esv32635	chr6:31141504-31250618	Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs9380220	HLA-F	Cis_chr	lymphoblastoid	RTeQTL
rs9380220	HLA-B	cis	lymphoblastoid	seeQTL
rs9380220	CCHCR1	cis	multi-tissue	Pritchard
rs9380220	TCF19	cis	lymphoblastoid	seeQTL
rs9380220	CCHCR1	Cis_1M	lymphoblastoid	RTeQTL
rs9380220	HLA-C	Cis_1M	lymphoblastoid	RTeQTL
rs9380220	HLA-B	Cis_1M	lymphoblastoid	RTeQTL
rs9380220	TCF19	Cis_1M	lymphoblastoid	RTeQTL
rs9380220	DDR1	cis	lymphoblastoid	seeQTL
rs9380220	CCHCR1	cis	lymphoblastoid	seeQTL
rs9380220	TCF19	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31127200-31146800	Weak transcription	Small Intestine	intestine
2	chr6:31127600-31147800	Weak transcription	Primary B cells from cord blood	blood
3	chr6:31127600-31148000	Weak transcription	Right Atrium	heart
4	chr6:31127800-31147800	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr6:31127800-31147800	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr6:31127800-31153200	Weak transcription	Rectal Smooth Muscle	rectum
7	chr6:31130400-31147800	Weak transcription	Stomach Smooth Muscle	stomach
8	chr6:31130600-31146800	Weak transcription	Colonic Mucosa	Colon
9	chr6:31131000-31147800	Weak transcription	Adipose Nuclei	Adipose
10	chr6:31131000-31148000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr6:31131000-31148000	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr6:31132000-31148000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr6:31133000-31148000	Weak transcription	Thymus	Thymus
14	chr6:31133000-31148200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr6:31138000-31146600	Weak transcription	Spleen	Spleen
16	chr6:31138000-31146800	Weak transcription	Hela-S3	cervix
17	chr6:31138000-31157400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr6:31139400-31148000	Weak transcription	Fetal Intestine Small	intestine
19	chr6:31141400-31146800	Weak transcription	Left Ventricle	heart
20	chr6:31141400-31148200	Weak transcription	Brain Germinal Matrix	brain
21	chr6:31141400-31148400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:31141600-31148000	Weak transcription	A549	lung
23	chr6:31141800-31152400	Weak transcription	HMEC	breast
24	chr6:31141800-31164800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr6:31142200-31147600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr6:31142800-31148800	Strong transcription	HepG2	liver
27	chr6:31143000-31146800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr6:31143200-31147800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr6:31143200-31151600	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr6:31143400-31147800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr6:31143400-31148000	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr6:31143800-31148000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr6:31144000-31146600	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr6:31144000-31146800	Weak transcription	Right Ventricle	heart
35	chr6:31144000-31147800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr6:31144000-31147800	Weak transcription	Fetal Stomach	stomach
37	chr6:31144000-31148200	Weak transcription	Esophagus	oesophagus
38	chr6:31144200-31146600	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr6:31144200-31146600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr6:31144200-31147800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr6:31144200-31147800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr6:31144200-31148000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr6:31144200-31148000	Weak transcription	Fetal Heart	heart
44	chr6:31144200-31148200	Weak transcription	Fetal Lung	lung
45	chr6:31144400-31146600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr6:31144400-31146600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr6:31144400-31146600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr6:31144400-31146600	Weak transcription	HSMM	muscle
49	chr6:31144400-31146800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr6:31144400-31146800	Weak transcription	NHDF-Ad	bronchial

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