Variant report

Variant	rs644452
Chromosome Location	chr6:31831944-31831945
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	PML	chr6:31831170-31832009	K562	blood:	n/a	n/a
2	MYC	chr6:31831293-31831968	K562	blood:	n/a	n/a
3	STAT3	chr6:31831483-31831967	MCF10A-Er-Src	breast:	n/a	chr6:31831814-31831825
4	HDAC2	chr6:31831255-31831945	HepG2	liver:	n/a	n/a
5	SP1	chr6:31831185-31831948	H1-hESC	embryonic stem cell:	n/a	n/a
6	POLR2A	chr6:31831325-31832002	HUVEC	blood vessel:	n/a	n/a
7	RAD21	chr6:31831262-31831962	H1-hESC	embryonic stem cell:	n/a	chr6:31831804-31831823
8	YY1	chr6:31830997-31832002	H1-hESC	embryonic stem cell:	n/a	n/a
9	SP1	chr6:31831127-31831966	A549	lung:	n/a	n/a
10	GATA1	chr6:31830424-31832058	PBDE	blood:	n/a	chr6:31830604-31830611 chr6:31830955-31830964
11	SIN3AK20	chr6:31831199-31831983	SK-N-SH	brain:	n/a	n/a
12	RAD21	chr6:31831255-31831972	ECC-1	luminal epithelium:	n/a	chr6:31831804-31831823
13	CTCF	chr6:31831325-31832118	K562	blood:	n/a	chr6:31831808-31831821 chr6:31831806-31831824 chr6:31831813-31831821
14	POLR2A	chr6:31829373-31832286	HepG2	liver:	n/a	n/a
15	POLR2A	chr6:31831102-31832010	PFSK-1	brain:	n/a	n/a
16	RAD21	chr6:31831369-31831972	IMR90	lung:	n/a	chr6:31831804-31831823
17	CTCF	chr6:31831315-31831966	MCF-7	breast:	n/a	chr6:31831808-31831821 chr6:31831806-31831824 chr6:31831813-31831821
18	MAX	chr6:31830311-31831945	ECC-1	luminal epithelium:	n/a	chr6:31830956-31830965
19	YY1	chr6:31831225-31831953	SK-N-SH_RA	brain:	n/a	n/a
20	MAX	chr6:31830301-31831977	A549	lung:	n/a	chr6:31830956-31830965
21	RAD21	chr6:31831575-31831957	K562	blood:	n/a	chr6:31831804-31831823
22	SP1	chr6:31830342-31831977	A549	lung:	n/a	chr6:31830892-31830901 chr6:31830892-31830901 chr6:31830647-31830656 chr6:31830890-31830902 chr6:31830890-31830902 chr6:31830678-31830699 chr6:31830891-31830900 chr6:31830851-31830872 chr6:31830891-31830901 chr6:31830891-31830901
23	ELF1	chr6:31831231-31831986	MCF-7	breast:	n/a	n/a
24	PML	chr6:31830232-31831968	K562	blood:	n/a	n/a
25	SMC3	chr6:31831406-31831970	Hela-S3	cervix:	n/a	chr6:31831808-31831822
26	CTCF	chr6:31831248-31832138	A549	lung:	n/a	chr6:31831808-31831821 chr6:31831806-31831824 chr6:31831813-31831821
27	MAX	chr6:31830091-31831957	K562	blood:	n/a	chr6:31830956-31830965
28	SIN3AK20	chr6:31829716-31832030	MCF-7	breast:	n/a	n/a
29	RAD21	chr6:31831321-31831965	HepG2	liver:	n/a	chr6:31831804-31831823
30	ZNF384	chr6:31830271-31832025	K562	blood:	n/a	n/a
31	RAD21	chr6:31831599-31831963	GM12878	blood:	n/a	chr6:31831804-31831823
32	CREB1	chr6:31830305-31831967	GM12878	blood:	n/a	chr6:31830879-31830892
33	RAD21	chr6:31831175-31832433	SK-N-SH	brain:	n/a	chr6:31831804-31831823
34	CTCF	chr6:31831420-31832005	K562	blood:	n/a	chr6:31831808-31831821 chr6:31831806-31831824 chr6:31831813-31831821
35	RAD21	chr6:31831581-31831981	Hela-S3	cervix:	n/a	chr6:31831804-31831823
36	SP1	chr6:31831153-31831975	H1-hESC	embryonic stem cell:	n/a	n/a
37	TEAD4	chr6:31831213-31831955	K562	blood:	n/a	n/a
38	MTA3	chr6:31831174-31832004	GM12878	blood:	n/a	n/a
39	PML	chr6:31831296-31831985	GM12878	blood:	n/a	n/a
40	GTF3C2	chr6:31830962-31832065	Hela-S3	cervix:	n/a	n/a
41	MAX	chr6:31831108-31831953	H1-hESC	embryonic stem cell:	n/a	n/a
42	YY1	chr6:31831030-31831952	K562	blood:	n/a	n/a
43	TRIM28	chr6:31830211-31832026	K562	blood:	n/a	n/a
44	MYBL2	chr6:31830251-31832006	HepG2	liver:	n/a	n/a
45	JUN	chr6:31829065-31833596	K562	blood:	n/a	chr6:31833071-31833080 chr6:31830957-31830966 chr6:31830955-31830967 chr6:31830385-31830394 chr6:31830953-31830964 chr6:31830860-31830869
46	POLR2A	chr6:31829585-31831955	K562	blood:	n/a	n/a
47	POLR2A	chr6:31831341-31832049	H1-neurons	neurons:	n/a	n/a
48	REST	chr6:31831142-31832135	H1-neurons	neurons:	n/a	chr6:31831552-31831565
49	SP1	chr6:31831152-31832000	HCT-116	colon:	n/a	n/a
50	POLR2A	chr6:31831260-31831993	PFSK-1	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:31830912..31833686-chr6:32013315..32015593,2	K562	blood:
2	chr6:31514420..31518271-chr6:31830053..31832008,3	K562	blood:
3	chr6:31743326..31746438-chr6:31828635..31833007,4	K562	blood:
4	chr6:31745070..31746845-chr6:31830028..31832915,2	MCF-7	breast:
5	chr6:31670174..31672313-chr6:31830988..31833810,3	K562	blood:
6	chr6:31830673..31832900-chr6:31938643..31940364,3	MCF-7	breast:
7	chr6:31830409..31832412-chr6:32014093..32016041,2	K562	blood:
8	chr6:31509002..31510673-chr6:31830602..31832330,2	K562	blood:
9	chr6:31761979..31764717-chr6:31829414..31832230,4	MCF-7	breast:
10	chr6:31800806..31810142-chr6:31827604..31833040,24	MCF-7	breast:
11	chr6:31781780..31785433-chr6:31828310..31832689,5	K562	blood:
12	chr6:31772422..31776496-chr6:31829254..31834757,6	K562	blood:
13	chr6:31828023..31833065-chr6:31863439..31869544,9	K562	blood:
14	chr6:31630209..31635577-chr6:31828786..31834874,28	K562	blood:
15	chr6:31831381..31833026-chr6:31853931..31855819,2	K562	blood:
16	chr6:31830083..31833987-chr6:31862759..31865610,4	MCF-7	breast:
17	chr6:31800580..31812447-chr6:31823435..31837480,47	K562	blood:
18	chr6:31801090..31813654-chr6:31824519..31834411,41	MCF-7	breast:
19	chr6:31794817..31797801-chr6:31829779..31831981,3	K562	blood:
20	chr6:31830894..31832674-chr6:31912375..31914374,2	MCF-7	breast:
21	chr6:31697145..31697789-chr6:31831310..31832181,3	K562	blood:
22	chr6:31630694..31635339-chr6:31828920..31834068,22	K562	blood:
23	chr6:31617566..31630444-chr6:31823885..31836000,84	K562	blood:
24	chr6:31829731..31832430-chr6:31863949..31866099,3	K562	blood:
25	chr6:31737530..31738235-chr6:31831315..31832267,3	K562	blood:
26	chr6:31781780..31785433-chr6:31829263..31832689,6	K562	blood:
27	chr6:31830500..31832979-chr6:31939876..31941891,3	K562	blood:
28	chr6:31706755..31708433-chr6:31830637..31832576,2	K562	blood:
29	chr6:31694918..31699964-chr6:31826467..31832957,9	K562	blood:
30	chr6:31831274..31833961-chr6:31853684..31856241,2	K562	blood:
31	chr6:31763390..31764233-chr6:31831287..31832195,2	MCF-7	breast:
32	chr6:31828958..31833712-chr6:31836982..31839801,4	MCF-7	breast:
33	chr6:31729872..31732091-chr6:31831679..31833339,2	K562	blood:
34	chr6:31711834..31714451-chr6:31829809..31833042,3	K562	blood:
35	chr6:31800755..31815108-chr6:31823340..31833266,54	K562	blood:
36	chr6:31793612..31800139-chr6:31830250..31833240,9	K562	blood:
37	chr6:31513172..31514702-chr6:31830028..31832398,2	MCF-7	breast:
38	chr6:31586339..31592286-chr6:31830032..31833457,6	K562	blood:
39	chr6:31701938..31704638-chr6:31828885..31832061,3	K562	blood:
40	chr6:31617566..31622844-chr6:31826455..31835211,65	K562	blood:
41	chr6:31630330..31634433-chr6:31829449..31833019,5	MCF-7	breast:
42	chr6:31830490..31833199-chr6:31923802..31927860,4	MCF-7	breast:
43	chr6:31697087..31699964-chr6:31831308..31832957,3	K562	blood:
44	chr6:31694971..31696688-chr6:31829211..31832001,2	MCF-7	breast:
45	chr6:31780296..31786175-chr6:31828333..31833086,7	MCF-7	breast:
46	chr6:31626270..31630199-chr6:31829030..31832230,7	K562	blood:

Variant related genes	Relation type
NEU1	TF binding region
ENSG00000204392	Chromatin interaction
ENSG00000254870	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000204427	Chromatin interaction
ENSG00000255152	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000201555	Chromatin interaction
ENSG00000204498	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000204410	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000200816	Chromatin interaction
ENSG00000243649	Chromatin interaction
ENSG00000204348	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000168477	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000204396	Chromatin interaction
ENSG00000204356	Chromatin interaction
ENSG00000213722	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000234006	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000201754	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000213760	Chromatin interaction
ENSG00000221267	Chromatin interaction
ENSG00000204351	Chromatin interaction
ENSG00000227198	Chromatin interaction
ENSG00000228727	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000201207	Chromatin interaction
ENSG00000204439	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000213719	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs2395079	0.85[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs3115673	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs480092	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4947253	0.84[ASN][1000 genomes]
rs565599	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57165260	0.81[ASN][1000 genomes]
rs613165	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs707926	0.82[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs743399	0.86[ASN][1000 genomes]
rs9767684	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	nsv884428	chr6:31728102-31870326	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
13	nsv884429	chr6:31730356-31837066	Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	155 gene(s)	inside rSNPs	diseases
14	nsv462872	chr6:31778272-31864304	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
15	nsv601945	chr6:31778272-31864304	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
16	nsv601950	chr6:31785438-32492308	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
17	nsv601951	chr6:31785438-32496748	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' 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	197 gene(s)	inside rSNPs	diseases
18	nsv601955	chr6:31785453-32484368	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
19	nsv601956	chr6:31785453-32492308	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
20	nsv462874	chr6:31794592-31864304	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
21	nsv601959	chr6:31794592-31864304	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
22	nsv884472	chr6:31813898-31870856	Weak transcription Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
23	nsv508399	chr6:31829474-31902423	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs644452	HSPA1B	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31829200-31832000	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr6:31829200-31832400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr6:31829400-31832200	Active TSS	HUES64 Cell Line	embryonic stem cell
4	chr6:31829400-31832400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr6:31829600-31832200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr6:31829600-31832200	Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr6:31829600-31832200	Active TSS	iPS-15b Cell Line	embryonic stem cell
8	chr6:31829600-31832200	Active TSS	HSMM	muscle
9	chr6:31829600-31832200	Active TSS	HSMMtube	muscle
10	chr6:31829600-31832200	Active TSS	NHDF-Ad	bronchial
11	chr6:31829600-31832400	Active TSS	H9 Cell Line	embryonic stem cell
12	chr6:31829800-31832200	Active TSS	Fetal Kidney	kidney
13	chr6:31829800-31832400	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr6:31829800-31832400	Active TSS	A549	lung
15	chr6:31830000-31832000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr6:31830000-31832000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr6:31830000-31832000	Active TSS	Ovary	ovary
18	chr6:31830000-31832000	Active TSS	Right Atrium	heart
19	chr6:31830000-31832200	Active TSS	iPS-20b Cell Line	embryonic stem cell
20	chr6:31830000-31832200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr6:31830000-31832200	Active TSS	Right Ventricle	heart
22	chr6:31830000-31832400	Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr6:31830000-31832400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
24	chr6:31830000-31832400	Bivalent/Poised TSS	HepG2	liver
25	chr6:31830200-31832000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr6:31830200-31832000	Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr6:31830200-31832000	Active TSS	Primary T helper naive cells from peripheral blood	blood
28	chr6:31830200-31832000	Active TSS	Cortex derived primary cultured neurospheres	brain
29	chr6:31830200-31832000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr6:31830200-31832000	Active TSS	Brain Cingulate Gyrus	brain
31	chr6:31830200-31832000	Active TSS	Psoas Muscle	Psoas
32	chr6:31830200-31832000	Active TSS	Rectal Smooth Muscle	rectum
33	chr6:31830200-31832200	Active TSS	H1 Cell Line	embryonic stem cell
34	chr6:31830200-31832200	Active TSS	iPS-18 Cell Line	embryonic stem cell
35	chr6:31830200-31832200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
36	chr6:31830200-31832200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr6:31830200-31832200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr6:31830200-31832200	Active TSS	Brain Germinal Matrix	brain
39	chr6:31830200-31832200	Active TSS	Brain Substantia Nigra	brain
40	chr6:31830200-31832200	Active TSS	Colon Smooth Muscle	Colon
41	chr6:31830200-31832200	Active TSS	Left Ventricle	heart
42	chr6:31830200-31832200	Active TSS	GM12878-XiMat	blood
43	chr6:31830200-31832400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr6:31830200-31832400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr6:31830200-31832400	Active TSS	Brain Angular Gyrus	brain
46	chr6:31830400-31832000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr6:31830400-31832000	Active TSS	Fetal Brain Female	brain
48	chr6:31830400-31832000	Active TSS	Fetal Lung	lung
49	chr6:31830400-31832000	Active TSS	Dnd41	blood
50	chr6:31830400-31832200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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