Variant report

Variant	rs805264
Chromosome Location	chr6:31623873-31623874
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TAF1	chr6:31623329-31623875	HepG2	liver:	n/a	n/a
2	FOXA1	chr6:31623196-31623952	HepG2	liver:	n/a	n/a
3	MYBL2	chr6:31622876-31624165	HepG2	liver:	n/a	n/a
4	TAF1	chr6:31623281-31623938	HepG2	liver:	n/a	n/a
5	TBP	chr6:31623227-31623893	HepG2	liver:	n/a	n/a
6	POLR2A	chr6:31622845-31624564	K562	blood:	n/a	n/a
7	FOSL2	chr6:31623222-31623884	HepG2	liver:	n/a	n/a
8	POLR2A	chr6:31623052-31624000	K562	blood:	n/a	n/a
9	POLR2A	chr6:31623182-31623987	H1-hESC	embryonic stem cell:	n/a	n/a
10	SIN3AK20	chr6:31623294-31623908	HepG2	liver:	n/a	n/a
11	NR2F2	chr6:31623397-31623964	K562	blood:	n/a	chr6:31623632-31623647
12	REST	chr6:31623255-31623942	HepG2	liver:	n/a	chr6:31623512-31623521
13	HEY1	chr6:31622963-31624708	HepG2	liver:	n/a	n/a
14	HNF4G	chr6:31623132-31623922	HepG2	liver:	n/a	chr6:31623452-31623467 chr6:31623635-31623647 chr6:31623629-31623644 chr6:31623450-31623468 chr6:31623453-31623465 chr6:31623452-31623467 chr6:31623452-31623467 chr6:31623448-31623470 chr6:31623635-31623653 chr6:31623637-31623650 chr6:31623637-31623651
15	RCOR1	chr6:31623321-31623898	HepG2	liver:	n/a	n/a
16	NFIC	chr6:31623036-31624026	HepG2	liver:	n/a	n/a
17	CEBPZ	chr6:31623220-31623952	HepG2	liver:	n/a	n/a
18	POLR2A	chr6:31623251-31624704	K562	blood:	n/a	n/a
19	HEY1	chr6:31623205-31624293	HepG2	liver:	n/a	n/a
20	TEAD4	chr6:31622990-31623927	HepG2	liver:	n/a	n/a
21	RXRA	chr6:31623223-31623891	HepG2	liver:	n/a	chr6:31623637-31623650 chr6:31623690-31623704 chr6:31623637-31623650 chr6:31623634-31623654 chr6:31623637-31623650
22	POLR2A	chr6:31623339-31623942	HepG2	liver:	n/a	n/a
23	POLR2A	chr6:31623145-31624640	HepG2	liver:	n/a	n/a
24	POLR2A	chr6:31623286-31624620	HepG2	liver:	n/a	n/a
25	NR2F2	chr6:31623103-31624072	HepG2	liver:	n/a	chr6:31623632-31623647
26	EP300	chr6:31622982-31623974	HepG2	liver:	n/a	n/a
27	MXI1	chr6:31623276-31623882	HepG2	liver:	n/a	n/a
28	HNF4A	chr6:31623179-31623931	HepG2	liver:	n/a	chr6:31623452-31623467 chr6:31623451-31623466 chr6:31623635-31623647 chr6:31623629-31623644 chr6:31623450-31623468 chr6:31623453-31623465 chr6:31623452-31623467 chr6:31623452-31623467 chr6:31623448-31623470 chr6:31623635-31623653 chr6:31623637-31623650 chr6:31623637-31623651
29	POLR2A	chr6:31623148-31623997	PFSK-1	brain:	n/a	n/a
30	CEBPD	chr6:31623410-31623945	HepG2	liver:	n/a	n/a
31	HDAC2	chr6:31623136-31623884	HepG2	liver:	n/a	chr6:31623486-31623505
32	MYBL2	chr6:31622600-31624667	HepG2	liver:	n/a	n/a
33	FOXA1	chr6:31623092-31623879	HepG2	liver:	n/a	n/a
34	POLR2A	chr6:31623174-31623943	HepG2	liver:	n/a	n/a
35	NFIC	chr6:31623074-31623986	HepG2	liver:	n/a	n/a
36	POLR2A	chr6:31623213-31623937	HepG2	liver:	n/a	n/a
37	POLR2A	chr6:31619380-31634380	HepG2	liver:	n/a	n/a
38	CEBPD	chr6:31623381-31623874	HepG2	liver:	n/a	n/a
39	YY1	chr6:31623184-31624018	HepG2	liver:	n/a	chr6:31623929-31623945 chr6:31623930-31623952
40	FOSL2	chr6:31623293-31623950	HepG2	liver:	n/a	n/a
41	MBD4	chr6:31622665-31624640	HepG2	liver:	n/a	n/a
42	MBD4	chr6:31622806-31624006	HepG2	liver:	n/a	n/a
43	POLR2A	chr6:31623607-31624179	K562	blood:	n/a	n/a
44	HNF4A	chr6:31623222-31623876	HepG2	liver:	n/a	chr6:31623452-31623467 chr6:31623451-31623466 chr6:31623635-31623647 chr6:31623629-31623644 chr6:31623450-31623468 chr6:31623453-31623465 chr6:31623452-31623467 chr6:31623452-31623467 chr6:31623448-31623470 chr6:31623635-31623653 chr6:31623637-31623650 chr6:31623637-31623651
45	POLR2A	chr6:31622876-31624723	HepG2	liver:	n/a	n/a
46	SP1	chr6:31623089-31624005	HepG2	liver:	n/a	n/a
47	POLR2A	chr6:31622582-31624398	SK-N-MC	brain:	n/a	n/a
48	HNF4G	chr6:31623146-31623913	HepG2	liver:	n/a	chr6:31623452-31623467 chr6:31623635-31623647 chr6:31623629-31623644 chr6:31623450-31623468 chr6:31623453-31623465 chr6:31623452-31623467 chr6:31623452-31623467 chr6:31623448-31623470 chr6:31623635-31623653 chr6:31623637-31623650 chr6:31623637-31623651
49	SIN3AK20	chr6:31623194-31623946	HepG2	liver:	n/a	n/a
50	YY1	chr6:31623321-31623915	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31623842-31623892	HepG2	liver:	n/a
2	chr6:31623842-31623892	AG04450	lung:	fetal
3	chr6:31623842-31623892	HUVEC	blood vessel:	n/a
4	chr6:31623842-31623892	PrEC	prostate:	n/a
5	chr6:31623842-31623892	LNCaP	prostate:	n/a
6	chr6:31623842-31623892	SAEC	small airway:	n/a
7	chr6:31623842-31623892	HRCEpiC	kidney:	n/a
8	chr6:31623842-31623892	NT2-D1	testis:	n/a
9	chr6:31623842-31623892	U87	brain:	n/a
10	chr6:31623842-31623892	HAEpiC	amniotic membrane:	n/a
11	chr6:31623842-31623892	PFSK-1	brain:	n/a
12	chr6:31623842-31623892	SK-N-SH_RA	brain:	n/a
13	chr6:31623842-31623892	T-47D	breast:	n/a
14	chr6:31623842-31623892	RPTEC	kidney:	n/a
15	chr6:31623842-31623892	HEEpiC	esophagus:	n/a
16	chr6:31623842-31623892	HPAEpiC	pulmonary alveolar:	n/a
17	chr6:31623842-31623892	HCPEpiC	choroid plexus:	n/a
18	chr6:31623842-31623892	Hela-S3	cervix:	n/a
19	chr6:31623842-31623892	HCM	heart:	n/a
20	chr6:31623842-31623892	HEK293	kidney:	embryo
21	chr6:31623842-31623892	HCT-116	colon:	n/a
22	chr6:31623842-31623892	H1-hESC	embryonic stem cell:	embryo
23	chr6:31623842-31623892	ECC-1	luminal epithelium:	n/a
24	chr6:31623842-31623892	AG04449	skin:	fetal
25	chr6:31623842-31623892	PANC-1	pancreas:	n/a
26	chr6:31623842-31623892	GM19239	blood:	n/a
27	chr6:31623842-31623892	BE2_C	brain:	n/a
28	chr6:31623842-31623892	CMK	blood:	n/a
29	chr6:31623842-31623892	HCF	heart:	n/a
30	chr6:31623842-31623892	HMEC	breast:	n/a
31	chr6:31623842-31623892	MCF10A-Er-Src	breast:	n/a
32	chr6:31623842-31623892	BJ	skin:	n/a
33	chr6:31623842-31623892	AG09319	gingival:	n/a
34	chr6:31623842-31623892	IMR90	lung:	fetal
35	chr6:31623842-31623892	AoSMC	blood vessel:	n/a
36	chr6:31623842-31623892	NHBE	bronchial:	n/a
37	chr6:31623842-31623892	Jurkat	blood:	n/a
38	chr6:31623842-31623892	HRPEpiC	eye:	n/a
39	chr6:31623842-31623892	HIPEpiC	eye:	n/a
40	chr6:31623842-31623892	AG10803	skin:	n/a
41	chr6:31623842-31623892	HRE	kidney:	n/a
42	chr6:31623842-31623892	SK-N-SH	brain:	n/a
43	chr6:31623842-31623892	NHDF-neo	bronchial:	n/a
44	chr6:31623842-31623892	Hepatocyte	liver:	n/a
45	chr6:31623842-31623892	SKMC	muscle:	n/a
46	chr6:31623842-31623892	SK-N-MC	brain:	n/a
47	chr6:31623842-31623892	MCF-7	breast:	n/a
48	chr6:31623842-31623892	GM06990	blood:	n/a
49	chr6:31623842-31623892	NH-A	brain:	n/a
50	chr6:31623842-31623892	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:31617566..31630444-chr6:31823885..31836000,84	K562	blood:
2	chr12:120729475..120730981-chr6:31623099..31625015,2	K562	blood:
3	chr6:31507451..31516055-chr6:31617949..31624791,11	MCF-7	breast:
4	chr6:31621359..31624108-chr6:31697605..31699324,2	MCF-7	breast:
5	chr6:31512932..31515167-chr6:31623848..31625863,2	K562	blood:

Variant related genes	Relation type
BAG6	TF binding region
C6orf47-AS1	TF binding region
BAG6	CpG island
C6orf47-AS1	CpG island
ENSG00000204385	Chromatin interaction
ENSG00000254870	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000204498	Chromatin interaction
ENSG00000213722	Chromatin interaction
ENSG00000213760	Chromatin interaction
ENSG00000265236	Chromatin interaction
ENSG00000202538	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000234006	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs12177823	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2075787	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2255741	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2736158	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2736161	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2736163	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2736165	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2736182	0.82[ASN][1000 genomes]
rs2857696	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3749952	0.86[ASN][1000 genomes]
rs4713479	0.86[ASN][1000 genomes]
rs707927	0.90[EUR][1000 genomes]
rs805258	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs805261	0.91[AFR][1000 genomes]
rs805263	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs805266	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs805267	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs805268	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs805269	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs805270	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs805272	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs805283	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs805291	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs805295	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs805298	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs805300	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9296001	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9461717	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9461718	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9461719	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9461721	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9469040	0.86[ASN][1000 genomes]
rs9469042	0.85[ASN][1000 genomes]
rs9469046	0.81[EUR][1000 genomes];0.89[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	nsv601609	chr6:31280101-31799786	Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
2	nsv601610	chr6:31280101-31960770	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	370 gene(s)	inside rSNPs	diseases
3	nsv601628	chr6:31280327-31990098	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
4	nsv601629	chr6:31280327-31996185	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
5	nsv601630	chr6:31280327-32011317	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
6	nsv601631	chr6:31280327-32017540	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
7	nsv1023939	chr6:31325961-32026747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
8	nsv538188	chr6:31325961-32026747	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
9	nsv432868	chr6:31338844-31721033	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	250 gene(s)	inside rSNPs	diseases
10	nsv1021747	chr6:31386219-31907266	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	330 gene(s)	inside rSNPs	diseases
11	nsv830627	chr6:31496214-31659950	Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
12	nsv884418	chr6:31525448-31741078	Active TSS Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	206 gene(s)	inside rSNPs	diseases
13	nsv1033154	chr6:31550614-32009410	Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	326 gene(s)	inside rSNPs	diseases
14	nsv462871	chr6:31575276-31632134	Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	133 gene(s)	inside rSNPs	diseases
15	nsv601942	chr6:31575276-31632134	Flanking Active TSS Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	133 gene(s)	inside rSNPs	diseases
16	nsv884419	chr6:31585000-31632651	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	138 gene(s)	inside rSNPs	diseases
17	nsv884420	chr6:31586827-31632651	Genic enhancers Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	138 gene(s)	inside rSNPs	diseases
18	nsv884421	chr6:31588151-31631907	Active TSS Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	129 gene(s)	inside rSNPs	diseases
19	nsv884422	chr6:31592524-31631907	Genic enhancers Enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	83 gene(s)	inside rSNPs	diseases
20	nsv884424	chr6:31593729-31632651	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	93 gene(s)	inside rSNPs	diseases
21	nsv1017945	chr6:31609641-32481240	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
22	esv3428142	chr6:31615800-31881809	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer 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	257 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31621200-31625000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:31621200-31625000	Weak transcription	Ovary	ovary
3	chr6:31621400-31624000	Enhancers	Fetal Intestine Large	intestine
4	chr6:31621400-31624200	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr6:31621400-31627600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr6:31621400-31627600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr6:31621600-31624200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr6:31621600-31624200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:31621600-31624200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:31621600-31624200	Weak transcription	Brain Angular Gyrus	brain
11	chr6:31621600-31624200	Weak transcription	Brain Cingulate Gyrus	brain
12	chr6:31621600-31624400	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr6:31621600-31624400	Weak transcription	Esophagus	oesophagus
14	chr6:31621600-31624800	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr6:31621600-31625000	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr6:31621600-31625000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr6:31621600-31625000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr6:31621600-31625000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr6:31621600-31625000	Weak transcription	Colon Smooth Muscle	Colon
20	chr6:31621600-31625000	Weak transcription	Fetal Lung	lung
21	chr6:31621600-31625000	Weak transcription	Stomach Mucosa	stomach
22	chr6:31621600-31625000	Weak transcription	NH-A	brain
23	chr6:31621600-31625200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr6:31621600-31625200	Weak transcription	Right Ventricle	heart
25	chr6:31621600-31625400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr6:31621600-31625400	Weak transcription	A549	lung
27	chr6:31621600-31625400	Weak transcription	HUVEC	blood vessel
28	chr6:31621600-31625400	Weak transcription	NHEK	skin
29	chr6:31621600-31625600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr6:31621600-31625800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr6:31621600-31625800	Weak transcription	HSMMtube	muscle
32	chr6:31621600-31626000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr6:31621600-31626000	Weak transcription	Psoas Muscle	Psoas
34	chr6:31621600-31626200	Weak transcription	Fetal Heart	heart
35	chr6:31621600-31626800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr6:31621600-31626800	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr6:31621600-31627000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:31621600-31627200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr6:31621600-31627200	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr6:31621600-31627200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr6:31621600-31627200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr6:31621600-31627400	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr6:31621600-31627400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr6:31621800-31624200	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr6:31621800-31624200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr6:31621800-31624200	Weak transcription	HSMM	muscle
47	chr6:31621800-31624400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr6:31621800-31624800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr6:31621800-31625000	Weak transcription	Primary B cells from peripheral blood	blood
50	chr6:31621800-31625000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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