Variant report

Variant	rs73402188
Chromosome Location	chr6:31832314-31832315
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:11)
CpG islands
(count:61)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:11 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:31832294-31833670	HepG2	liver:	n/a	n/a
2	POLR2A	chr6:31832042-31832626	HepG2	liver:	n/a	n/a
3	POLR2A	chr6:31832263-31834177	HepG2	liver:	n/a	n/a
4	RAD21	chr6:31831175-31832433	SK-N-SH	brain:	n/a	chr6:31831804-31831823
5	HEY1	chr6:31832079-31834004	HepG2	liver:	n/a	n/a
6	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
7	MXI1	chr6:31829645-31832562	SK-N-SH	brain:	n/a	chr6:31830718-31830727
8	MYBL2	chr6:31830178-31834219	HepG2	liver:	n/a	n/a
9	MBD4	chr6:31832021-31832625	HepG2	liver:	n/a	n/a
10	NR2F2	chr6:31829652-31832647	K562	blood:	n/a	n/a
11	HEY1	chr6:31832229-31833551	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31832313-31832363	SK-N-SH	brain:	n/a
2	chr6:31832313-31832363	HRPEpiC	eye:	n/a
3	chr6:31832313-31832363	BE2_C	brain:	n/a
4	chr6:31832313-31832363	MCF10A-Er-Src	breast:	n/a
5	chr6:31832313-31832363	GM12892	blood:	n/a
6	chr6:31832313-31832363	NT2-D1	testis:	n/a
7	chr6:31832313-31832363	K562	blood:	n/a
8	chr6:31832313-31832363	HCT-116	colon:	n/a
9	chr6:31832313-31832363	HPAEpiC	pulmonary alveolar:	n/a
10	chr6:31832313-31832363	T-47D	breast:	n/a
11	chr6:31832313-31832363	ECC-1	luminal epithelium:	n/a
12	chr6:31832313-31832363	PrEC	prostate:	n/a
13	chr6:31832313-31832363	NHDF-neo	bronchial:	n/a
14	chr6:31832313-31832363	Hepatocyte	liver:	n/a
15	chr6:31832313-31832363	HIPEpiC	eye:	n/a
16	chr6:31832313-31832363	NH-A	brain:	n/a
17	chr6:31832313-31832363	SAEC	small airway:	n/a
18	chr6:31832313-31832363	HCPEpiC	choroid plexus:	n/a
19	chr6:31832313-31832363	HEEpiC	esophagus:	n/a
20	chr6:31832313-31832363	BJ	skin:	n/a
21	chr6:31832313-31832363	LNCaP	prostate:	n/a
22	chr6:31832313-31832363	GM12891	blood:	n/a
23	chr6:31832313-31832363	HCM	heart:	n/a
24	chr6:31832313-31832363	AG04449	skin:	fetal
25	chr6:31832313-31832363	HRCEpiC	kidney:	n/a
26	chr6:31832313-31832363	HAEpiC	amniotic membrane:	n/a
27	chr6:31832313-31832363	MCF-7	breast:	n/a
28	chr6:31832313-31832363	A549	lung:	n/a
29	chr6:31832313-31832363	ovcar-3	ovarian:	n/a
30	chr6:31832313-31832363	SK-N-MC	brain:	n/a
31	chr6:31832313-31832363	IMR90	lung:	fetal
32	chr6:31832313-31832363	GM06990	blood:	n/a
33	chr6:31832313-31832363	HUVEC	blood vessel:	n/a
34	chr6:31832313-31832363	AG09309	skin:	n/a
35	chr6:31832313-31832363	RPTEC	kidney:	n/a
36	chr6:31832313-31832363	AoSMC	blood vessel:	n/a
37	chr6:31832313-31832363	SK-N-SH_RA	brain:	n/a
38	chr6:31832313-31832363	HCF	heart:	n/a
39	chr6:31832313-31832363	ProgFib	skin:	n/a
40	chr6:31832313-31832363	HL-60	blood:	n/a
41	chr6:31832313-31832363	HepG2	liver:	n/a
42	chr6:31832313-31832363	SKMC	muscle:	n/a
43	chr6:31832313-31832363	H1-hESC	embryonic stem cell:	embryo
44	chr6:31832313-31832363	PANC-1	pancreas:	n/a
45	chr6:31832313-31832363	Jurkat	blood:	n/a
46	chr6:31832313-31832363	U87	brain:	n/a
47	chr6:31832313-31832363	PFSK-1	brain:	n/a
48	chr6:31832313-31832363	Caco-2	colon:	n/a
49	chr6:31832313-31832363	GM19239	blood:	n/a
50	chr6:31832313-31832363	AG04450	lung:	fetal

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31830912..31833686-chr6:32013315..32015593,2	K562	blood:
2	chr6:31743326..31746438-chr6:31828635..31833007,4	K562	blood:
3	chr6:31745070..31746845-chr6:31830028..31832915,2	MCF-7	breast:
4	chr6:31670174..31672313-chr6:31830988..31833810,3	K562	blood:
5	chr6:31830673..31832900-chr6:31938643..31940364,3	MCF-7	breast:
6	chr6:31830409..31832412-chr6:32014093..32016041,2	K562	blood:
7	chr6:31774180..31776496-chr6:31832190..31834757,3	K562	blood:
8	chr6:31509002..31510673-chr6:31830602..31832330,2	K562	blood:
9	chr6:31800806..31810142-chr6:31827604..31833040,24	MCF-7	breast:
10	chr6:31781780..31785433-chr6:31828310..31832689,5	K562	blood:
11	chr6:31772422..31776496-chr6:31829254..31834757,6	K562	blood:
12	chr6:31832130..31834569-chr6:31860075..31862005,2	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	chr6:31830894..31832674-chr6:31912375..31914374,2	MCF-7	breast:
20	chr6:31630694..31635339-chr6:31828920..31834068,22	K562	blood:
21	chr6:31617566..31630444-chr6:31823885..31836000,84	K562	blood:
22	chr6:31829731..31832430-chr6:31863949..31866099,3	K562	blood:
23	chr6:31781780..31785433-chr6:31829263..31832689,6	K562	blood:
24	chr6:31830500..31832979-chr6:31939876..31941891,3	K562	blood:
25	chr6:31706755..31708433-chr6:31830637..31832576,2	K562	blood:
26	chr6:31694918..31699964-chr6:31826467..31832957,9	K562	blood:
27	chr6:31831274..31833961-chr6:31853684..31856241,2	K562	blood:
28	chr6:31828958..31833712-chr6:31836982..31839801,4	MCF-7	breast:
29	chr6:31729872..31732091-chr6:31831679..31833339,2	K562	blood:
30	chr6:31711834..31714451-chr6:31829809..31833042,3	K562	blood:
31	chr6:31800755..31815108-chr6:31823340..31833266,54	K562	blood:
32	chr6:31793612..31800139-chr6:31830250..31833240,9	K562	blood:
33	chr6:31513172..31514702-chr6:31830028..31832398,2	MCF-7	breast:
34	chr6:31586339..31592286-chr6:31830032..31833457,6	K562	blood:
35	chr6:31617566..31622844-chr6:31826455..31835211,65	K562	blood:
36	chr6:31630330..31634433-chr6:31829449..31833019,5	MCF-7	breast:
37	chr6:31830490..31833199-chr6:31923802..31927860,4	MCF-7	breast:
38	chr6:31697087..31699964-chr6:31831308..31832957,3	K562	blood:
39	chr6:31780296..31786175-chr6:31828333..31833086,7	MCF-7	breast:

No data

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

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs11961829	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11964923	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73398298	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73402181	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73404118	0.94[AFR][1000 genomes];1.00[AMR][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

No data

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31829200-31832400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr6:31829400-31832400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr6:31829600-31832400	Active TSS	H9 Cell Line	embryonic stem cell
4	chr6:31829800-31832400	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chr6:31829800-31832400	Active TSS	A549	lung
6	chr6:31830000-31832400	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr6:31830000-31832400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
8	chr6:31830000-31832400	Bivalent/Poised TSS	HepG2	liver
9	chr6:31830200-31832400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:31830200-31832400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:31830200-31832400	Active TSS	Brain Angular Gyrus	brain
12	chr6:31830400-31832400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr6:31830400-31832400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr6:31830800-31832400	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr6:31830800-31845200	Weak transcription	Small Intestine	intestine
16	chr6:31831000-31832400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr6:31831000-31832400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr6:31831000-31834200	Genic enhancers	Stomach Mucosa	stomach
19	chr6:31831200-31832400	Flanking Active TSS	Stomach Smooth Muscle	stomach
20	chr6:31831200-31832600	Enhancers	Fetal Heart	heart
21	chr6:31831200-31832600	Genic enhancers	Gastric	stomach
22	chr6:31831400-31832400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr6:31831400-31832400	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
24	chr6:31831400-31832800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr6:31831600-31832400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr6:31831600-31832400	Active TSS	Brain Hippocampus Middle	brain
27	chr6:31831800-31832400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr6:31831800-31832400	Active TSS	HMEC	breast
29	chr6:31831800-31832600	Enhancers	Spleen	Spleen
30	chr6:31831800-31833400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr6:31831800-31834000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr6:31831800-31845000	Weak transcription	Lung	lung
33	chr6:31832000-31832400	Enhancers	Primary B cells from cord blood	blood
34	chr6:31832000-31832400	Enhancers	Primary B cells from peripheral blood	blood
35	chr6:31832000-31832400	Enhancers	Primary T cells fromperipheralblood	blood
36	chr6:31832000-31832400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr6:31832000-31832400	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr6:31832000-31832400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr6:31832000-31832400	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr6:31832000-31832400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr6:31832000-31832400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr6:31832000-31832400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
43	chr6:31832000-31832400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
44	chr6:31832000-31832400	Flanking Active TSS	Brain Cingulate Gyrus	brain
45	chr6:31832000-31832400	Active TSS	Brain Inferior Temporal Lobe	brain
46	chr6:31832000-31832400	Flanking Active TSS	Fetal Brain Female	brain
47	chr6:31832000-31832400	Enhancers	Pancreas	Pancrea
48	chr6:31832000-31832400	Genic enhancers	Rectal Mucosa Donor 31	rectum
49	chr6:31832000-31832400	Enhancers	NH-A	brain
50	chr6:31832000-31832400	Enhancers	NHLF	lung

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