Variant report

Variant	rs6913120
Chromosome Location	chr6:5260505-5260506
allele	A/G
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	MYC	chr6:5260300-5261943	K562	blood:	n/a	chr6:5261926-5261935 chr6:5261528-5261538 chr6:5261646-5261656
2	POLR2A	chr6:5260212-5262541	GM12891	blood:	n/a	n/a
3	POLR2A	chr6:5260263-5260822	K562	blood:	n/a	n/a
4	TAF1	chr6:5260316-5262128	H1-hESC	embryonic stem cell:	n/a	n/a
5	RCOR1	chr6:5260285-5262012	K562	blood:	n/a	n/a
6	MAX	chr6:5260382-5262148	HCT-116	colon:	n/a	chr6:5261926-5261935 chr6:5261528-5261538 chr6:5261646-5261656
7	MAX	chr6:5260392-5262027	ECC-1	luminal epithelium:	n/a	chr6:5261926-5261935 chr6:5261528-5261538 chr6:5261646-5261656
8	EGR1	chr6:5260477-5262006	MCF-7	breast:	n/a	chr6:5261783-5261807 chr6:5261237-5261250 chr6:5261920-5261942 chr6:5261237-5261250 chr6:5261237-5261247 chr6:5261930-5261937 chr6:5261927-5261936 chr6:5261777-5261786 chr6:5261237-5261250 chr6:5261234-5261248 chr6:5261236-5261250 chr6:5261156-5261169 chr6:5261238-5261247 chr6:5261237-5261250 chr6:5261191-5261205 chr6:5261285-5261295
9	HCFC1	chr6:5260243-5262113	K562	blood:	n/a	n/a
10	CREB1	chr6:5260293-5262056	GM12878	blood:	n/a	n/a
11	ATF1	chr6:5260289-5260755	K562	blood:	n/a	n/a
12	MXI1	chr6:5260273-5262162	HepG2	liver:	n/a	chr6:5261474-5261489
13	MAX	chr6:5260150-5262141	HepG2	liver:	n/a	chr6:5261926-5261935 chr6:5261528-5261538 chr6:5261646-5261656
14	ZMIZ1	chr6:5260311-5260774	K562	blood:	n/a	n/a
15	IRF1	chr6:5260310-5261965	K562	blood:	n/a	chr6:5261504-5261518 chr6:5261194-5261208 chr6:5261221-5261235 chr6:5261232-5261246
16	POLR2A	chr6:5260122-5262141	SK-N-MC	brain:	n/a	n/a
17	MXI1	chr6:5260305-5262442	Hela-S3	cervix:	n/a	chr6:5261474-5261489
18	UBTF	chr6:5260307-5260714	K562	blood:	n/a	n/a
19	JUND	chr6:5260301-5262032	K562	blood:	n/a	n/a
20	HCFC1	chr6:5259374-5262547	Hela-S3	cervix:	n/a	n/a
21	MXI1	chr6:5259910-5262664	SK-N-SH	brain:	n/a	chr6:5261474-5261489
22	POLR2A	chr6:5259206-5262355	MCF10A-Er-Src	breast:	n/a	n/a
23	ETS1	chr6:5260490-5262001	K562	blood:	n/a	chr6:5261239-5261250
24	UBTF	chr6:5260314-5262005	K562	blood:	n/a	n/a
25	POLR2A	chr6:5260367-5262627	GM12892	blood:	n/a	n/a
26	CTCF	chr6:5260380-5260530	HepG2	liver:	n/a	n/a
27	POLR2A	chr6:5260322-5262005	K562	blood:	n/a	n/a
28	CTCF	chr6:5260380-5260530	HEK293	kidney:	n/a	n/a
29	POLR2A	chr6:5260349-5262284	Raji	blood:	n/a	n/a
30	POLR2A	chr6:5260141-5261246	GM12892	blood:	n/a	n/a
31	MAFK	chr6:5260200-5260671	K562	blood:	n/a	n/a
32	POLR2A	chr6:5260434-5261195	ProgFib	skin:	n/a	n/a
33	SMC3	chr6:5260090-5262382	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr6:5260251-5260814	GM12891	blood:	n/a	n/a
35	TFAP2C	chr6:5260377-5262010	Hela-S3	cervix:	n/a	n/a
36	MYC	chr6:5259692-5261974	MCF10A-Er-Src	breast:	n/a	chr6:5261926-5261935 chr6:5261528-5261538 chr6:5259845-5259856 chr6:5261646-5261656
37	POLR2A	chr6:5260194-5262496	HepG2	liver:	n/a	n/a
38	JUN	chr6:5260099-5262034	K562	blood:	n/a	n/a
39	MAZ	chr6:5260449-5261965	GM12878	blood:	n/a	chr6:5261926-5261935 chr6:5261528-5261538 chr6:5261646-5261656
40	GTF2F1	chr6:5260253-5261925	Hela-S3	cervix:	n/a	n/a
41	ZNF384	chr6:5260251-5261962	K562	blood:	n/a	n/a
42	POLR2A	chr6:5260323-5262026	NB4	blood:	n/a	n/a
43	YY1	chr6:5260457-5262016	K562	blood:	n/a	chr6:5261761-5261769 chr6:5261762-5261772 chr6:5261750-5261772 chr6:5261087-5261101 chr6:5261552-5261566 chr6:5261755-5261774 chr6:5261239-5261248 chr6:5261162-5261176
44	POLR2A	chr6:5260473-5262056	GM19193	blood:	n/a	n/a
45	YY1	chr6:5260389-5262222	A549	lung:	n/a	chr6:5261761-5261769 chr6:5261762-5261772 chr6:5261750-5261772 chr6:5261087-5261101 chr6:5261552-5261566 chr6:5261755-5261774 chr6:5261239-5261248 chr6:5261162-5261176
46	POLR2A	chr6:5260501-5262037	HEK293	kidney:	n/a	n/a
47	REST	chr6:5260305-5262354	H1-neurons	neurons:	n/a	n/a
48	POLR2A	chr6:5260332-5261458	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr6:5260306-5260810	GM12891	blood:	n/a	n/a
50	POLR2A	chr6:5260231-5261993	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:150038831..150039716-chr6:5260490..5261436,2	Hela-S3	cervix:
2	chr6:5230476..5232022-chr6:5258422..5260596,2	MCF-7	breast:

Variant related genes	Relation type
FARS2	TF binding region
ENSG00000136631	Chromatin interaction

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs11752747	0.91[EUR][1000 genomes]
rs12174086	0.84[ASN][1000 genomes]
rs13191012	0.94[ASN][1000 genomes]
rs1570085	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1609808	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17139985	0.99[ASN][1000 genomes]
rs1884976	0.80[ASN][1000 genomes]
rs2145372	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2224391	1.00[ASN][1000 genomes]
rs2224392	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2753214	0.80[ASN][1000 genomes]
rs2753222	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2753223	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2753224	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2753228	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2753229	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2753230	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2753233	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2753234	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2753235	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2753236	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2753237	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2753238	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2753239	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2753240	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2753243	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2753244	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2753245	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2753246	0.99[ASN][1000 genomes]
rs2753247	0.99[ASN][1000 genomes]
rs2753248	0.99[ASN][1000 genomes]
rs2753249	0.99[ASN][1000 genomes]
rs2773296	0.83[ASN][1000 genomes]
rs2773298	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2773299	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2773300	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2773302	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2773304	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2773306	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2773307	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2773308	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2773309	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2773310	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2773311	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2773312	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2773314	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2773316	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2773317	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2773318	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2773319	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2773320	0.99[ASN][1000 genomes]
rs2773322	0.99[ASN][1000 genomes]
rs35048711	0.93[ASN][1000 genomes]
rs36055504	0.94[ASN][1000 genomes]
rs6909619	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6925249	0.99[ASN][1000 genomes]
rs766339	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs766340	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7752203	1.00[ASN][1000 genomes]
rs7758400	0.88[ASN][1000 genomes]
rs928170	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9328289	0.82[ASN][1000 genomes]
rs9378420	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9378943	0.83[ASN][1000 genomes]
rs9392665	0.92[ASN][1000 genomes]
rs9392666	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9405259	0.81[ASN][1000 genomes]
rs9405260	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9405809	0.90[ASN][1000 genomes]
rs9405811	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9405813	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9504364	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9504365	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9504368	0.95[ASN][1000 genomes]
rs9504369	0.99[ASN][1000 genomes]
rs9504371	0.99[ASN][1000 genomes]
rs9784870	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023527	chr6:4729592-5387176	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv600872	chr6:4975313-5342190	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats 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 miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1031837	chr6:4996667-5418726	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Strong transcription 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	23 gene(s)	inside rSNPs	diseases
4	nsv1034681	chr6:5070351-5387176	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
5	nsv538113	chr6:5070351-5387176	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS 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	15 gene(s)	inside rSNPs	diseases
6	nsv1018152	chr6:5077025-5387176	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
7	nsv600873	chr6:5089278-5400658	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription 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	12 gene(s)	inside rSNPs	diseases
8	nsv1030254	chr6:5132261-5431585	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
9	nsv1034463	chr6:5137959-5345678	Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
10	nsv1021646	chr6:5157795-5367254	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription 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	8 gene(s)	inside rSNPs	diseases
11	nsv538115	chr6:5157795-5367254	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	nsv1029609	chr6:5187633-5397254	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
13	nsv1035080	chr6:5206533-5396019	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
14	nsv538116	chr6:5206533-5396019	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
15	nsv1016456	chr6:5216835-5315913	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
16	nsv538117	chr6:5216835-5315913	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
17	nsv1019428	chr6:5216835-5627839	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
18	nsv538118	chr6:5216835-5627839	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
19	nsv522457	chr6:5245070-5260936	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
20	nsv1028185	chr6:5247624-5340163	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr6:5259600-5260600	Flanking Active TSS	Dnd41	blood
2	chr6:5259600-5263000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr6:5259600-5263200	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr6:5259800-5260600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:5259800-5260600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr6:5259800-5260600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr6:5259800-5260600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr6:5259800-5260600	Flanking Active TSS	Brain Angular Gyrus	brain
9	chr6:5259800-5260600	Flanking Active TSS	Brain Germinal Matrix	brain
10	chr6:5259800-5260600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
11	chr6:5259800-5260600	Flanking Active TSS	Duodenum Mucosa	Duodenum
12	chr6:5259800-5260600	Flanking Active TSS	Fetal Brain Female	brain
13	chr6:5259800-5260800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr6:5259800-5262200	Active TSS	Stomach Smooth Muscle	stomach
15	chr6:5259800-5262800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr6:5259800-5262800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr6:5259800-5263200	Active TSS	HUES48 Cell Line	embryonic stem cell
18	chr6:5260000-5260600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr6:5260000-5260600	Flanking Active TSS	Primary hematopoietic stem cells	blood
20	chr6:5260000-5260600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
21	chr6:5260000-5260600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
22	chr6:5260000-5260600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
23	chr6:5260000-5260600	Flanking Active TSS	Liver	Liver
24	chr6:5260000-5260600	Flanking Active TSS	Brain Cingulate Gyrus	brain
25	chr6:5260000-5260600	Flanking Active TSS	Brain Substantia Nigra	brain
26	chr6:5260000-5260600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
27	chr6:5260000-5260600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
28	chr6:5260000-5260600	Flanking Active TSS	Rectal Smooth Muscle	rectum
29	chr6:5260000-5260600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
30	chr6:5260000-5260600	Flanking Active TSS	HUVEC	blood vessel
31	chr6:5260000-5260600	Flanking Active TSS	NH-A	brain
32	chr6:5260000-5260600	Flanking Active TSS	NHLF	lung
33	chr6:5260000-5260600	Flanking Active TSS	Osteobl	bone
34	chr6:5260000-5260800	Flanking Active TSS	Adipose Nuclei	Adipose
35	chr6:5260000-5260800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr6:5260000-5261000	Active TSS	Right Atrium	heart
37	chr6:5260000-5262800	Active TSS	A549	lung
38	chr6:5260000-5262800	Active TSS	NHDF-Ad	bronchial
39	chr6:5260000-5263000	Active TSS	H1 Cell Line	embryonic stem cell
40	chr6:5260000-5263000	Active TSS	iPS-18 Cell Line	embryonic stem cell
41	chr6:5260000-5263000	Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr6:5260000-5263000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr6:5260000-5263000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr6:5260000-5263000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr6:5260000-5263200	Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr6:5260000-5263200	Active TSS	HUES6 Cell Line	embryonic stem cell
47	chr6:5260000-5263200	Active TSS	K562	blood
48	chr6:5260200-5260600	Flanking Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr6:5260200-5260600	Flanking Active TSS	Primary B cells from cord blood	blood
50	chr6:5260200-5260600	Flanking Active TSS	Primary B cells from peripheral blood	blood

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