Variant report

Variant	rs145154321
Chromosome Location	chr6:31783881-31783882
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:75)
CpG islands
(count:0)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:75 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOSL2	chr6:31782902-31784606	HepG2	liver:	n/a	chr6:31783163-31783172 chr6:31783185-31783194 chr6:31782927-31782936
2	GABPA	chr6:31783245-31783921	Hela-S3	cervix:	n/a	n/a
3	POLR2A	chr6:31782886-31785389	GM12878	blood:	n/a	n/a
4	REST	chr6:31783458-31784083	U87	brain:	n/a	n/a
5	REST	chr6:31783673-31784087	HepG2	liver:	n/a	n/a
6	POLR2A	chr6:31783040-31783905	GM12878	blood:	n/a	n/a
7	MYC	chr6:31783880-31784139	MCF-7	breast:	n/a	n/a
8	JUND	chr6:31783031-31785499	HepG2	liver:	n/a	chr6:31783163-31783172 chr6:31783185-31783194
9	TAF1	chr6:31782938-31785439	HepG2	liver:	n/a	n/a
10	POLR2A	chr6:31782425-31784264	A549	lung:	n/a	n/a
11	REST	chr6:31783696-31784132	GM12878	blood:	n/a	n/a
12	POU2F2	chr6:31783043-31784000	GM12878	blood:	n/a	n/a
13	POLR2A	chr6:31783013-31785321	GM12892	blood:	n/a	n/a
14	MYC	chr6:31783435-31784258	MCF-7	breast:	n/a	n/a
15	HEY1	chr6:31782870-31785566	K562	blood:	n/a	n/a
16	MYC	chr6:31783561-31784136	MCF-7	breast:	n/a	n/a
17	IRF4	chr6:31783391-31784161	GM12878	blood:	n/a	n/a
18	POLR2A	chr6:31782906-31785452	Hela-S3	cervix:	n/a	n/a
19	TCF3	chr6:31783282-31784737	GM12878	blood:	n/a	n/a
20	CTCF	chr6:31783876-31783911	Lung_OC	lung:	n/a	n/a
21	POLR2A	chr6:31782925-31784216	HepG2	liver:	n/a	n/a
22	PAX5	chr6:31783175-31784147	GM12878	blood:	n/a	n/a
23	CBX3	chr6:31781275-31785537	K562	blood:	n/a	n/a
24	POLR2A	chr6:31781587-31785535	Hela-S3	cervix:	n/a	n/a
25	PAX5	chr6:31783083-31784105	GM12878	blood:	n/a	n/a
26	POLR2A	chr6:31782933-31784151	HepG2	liver:	n/a	n/a
27	POLR2A	chr6:31782845-31785326	A549	lung:	n/a	n/a
28	POLR2A	chr6:31782935-31784154	A549	lung:	n/a	n/a
29	POLR2A	chr6:31782305-31785408	MCF-7	breast:	n/a	n/a
30	POLR2A	chr6:31783476-31784215	H1-hESC	embryonic stem cell:	n/a	n/a
31	STAT5A	chr6:31782916-31784075	K562	blood:	n/a	n/a
32	POLR2A	chr6:31781939-31787367	K562	blood:	n/a	n/a
33	REST	chr6:31783739-31784032	SK-N-SH	brain:	n/a	n/a
34	POLR2A	chr6:31782260-31785385	MCF-7	breast:	n/a	n/a
35	POLR2A	chr6:31782025-31784136	HUVEC	blood vessel:	n/a	n/a
36	NR2F2	chr6:31781154-31786921	K562	blood:	n/a	n/a
37	POLR2A	chr6:31782841-31785468	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr6:31783449-31783945	K562	blood:	n/a	n/a
39	TRIM28	chr6:31782257-31784210	K562	blood:	n/a	n/a
40	REST	chr6:31783628-31784081	SK-N-SH	brain:	n/a	n/a
41	REST	chr6:31783596-31784114	H1-hESC	embryonic stem cell:	n/a	n/a
42	POU2F2	chr6:31783039-31784103	GM12891	blood:	n/a	n/a
43	POLR2A	chr6:31782107-31783937	PANC-1	pancreas:	n/a	n/a
44	POLR2A	chr6:31782403-31785399	H1-hESC	embryonic stem cell:	n/a	n/a
45	HEY1	chr6:31783150-31785545	K562	blood:	n/a	n/a
46	POLR2A	chr6:31782467-31785416	MCF-7	breast:	n/a	n/a
47	REST	chr6:31783471-31784120	PFSK-1	brain:	n/a	n/a
48	POLR2A	chr6:31783015-31785484	GM12878	blood:	n/a	n/a
49	POLR2A	chr6:31782853-31785455	GM12878	blood:	n/a	n/a
50	POLR2A	chr6:31782928-31785486	GM12878	blood:	n/a	n/a

No data

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31781796..31783894-chr6:31925428..31927086,2	K562	blood:
2	chr6:31781417..31783934-chr6:32937499..32939420,2	K562	blood:
3	chr6:31782856..31784391-chr6:31887336..31890005,2	MCF-7	breast:
4	chr6:31780821..31784746-chr6:31829825..31831701,4	MCF-7	breast:
5	chr6:31619043..31621335-chr6:31782938..31784758,2	MCF-7	breast:
6	chr6:31507867..31510784-chr6:31781026..31784406,3	MCF-7	breast:
7	chr6:31782025..31784864-chr6:32163977..32165547,2	K562	blood:
8	chr6:31781780..31785433-chr6:31828310..31832689,5	K562	blood:
9	chr6:31513245..31516542-chr6:31782394..31785632,3	MCF-7	breast:
10	chr6:31781780..31785433-chr6:31829263..31832689,6	K562	blood:
11	chr6:31743107..31747994-chr6:31781956..31785553,7	MCF-7	breast:
12	chr6:31587709..31590301-chr6:31782411..31784104,4	MCF-7	breast:
13	chr6:31780296..31786175-chr6:31828333..31833086,7	MCF-7	breast:
14	chr6:31630940..31635916-chr6:31782579..31784659,6	MCF-7	breast:
15	chr6:31759482..31765185-chr6:31781824..31784897,13	MCF-7	breast:
16	chr6:31782860..31784585-chr6:31867498..31869267,2	K562	blood:
17	chr15:45315050..45315829-chr6:31783366..31783889,2	Hela-S3	cervix:
18	chr6:31756951..31764627-chr6:31780500..31799197,32	MCF-7	breast:
19	chr6:31508732..31511014-chr6:31781931..31784408,2	K562	blood:
20	chr6:31781258..31784668-chr6:32935964..32938963,3	MCF-7	breast:
21	chr6:31781426..31784987-chr6:31937458..31940746,3	K562	blood:
22	chr6:31780574..31784383-chr6:31865157..31867218,4	K562	blood:

No data

Variant related genes	Relation type
HSPA1L	TF binding region
ENSG00000204444	Chromatin interaction
ENSG00000204356	Chromatin interaction
ENSG00000254870	Chromatin interaction
ENSG00000213760	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000204498	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000204348	Chromatin interaction
ENSG00000204256	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000204351	Chromatin interaction
ENSG00000140263	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000223837	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000265236	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000234006	Chromatin interaction
ENSG00000204396	Chromatin interaction
ENSG00000204301	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000204257	Chromatin interaction
ENSG00000201555	Chromatin interaction
ENSG00000201207	Chromatin interaction
ENSG00000204344	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:29 , 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	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
10	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
11	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
12	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
13	nsv884426	chr6:31728102-31800868	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
14	nsv884427	chr6:31728102-31802465	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers 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 target site	152 gene(s)	inside rSNPs	diseases
15	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
16	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
17	nsv884430	chr6:31731881-31800631	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
18	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
19	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
20	nsv981359	chr6:31779004-31797103	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	111 gene(s)	inside rSNPs	diseases
21	nsv869989	chr6:31779203-31797657	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	114 gene(s)	inside rSNPs	diseases
22	nsv601946	chr6:31782617-31795082	Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	85 gene(s)	inside rSNPs	diseases
23	nsv482094	chr6:31783291-31785719	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	50 gene(s)	inside rSNPs	diseases
24	esv3344240	chr6:31783339-31795664	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	106 gene(s)	inside rSNPs	diseases
25	nsv823504	chr6:31783490-31795322	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	88 gene(s)	inside rSNPs	diseases
26	nsv884448	chr6:31783527-31794592	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
27	nsv884449	chr6:31783527-31795082	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	75 gene(s)	inside rSNPs	diseases
28	nsv884450	chr6:31783527-31797769	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
29	nsv884451	chr6:31783527-31800631	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	105 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31782200-31785200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:31782800-31785200	Weak transcription	Fetal Heart	heart
3	chr6:31783600-31785000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:31783600-31785000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr6:31783600-31785000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr6:31783600-31785000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr6:31783600-31785000	Weak transcription	Brain Angular Gyrus	brain
8	chr6:31783600-31785000	Weak transcription	Brain Cingulate Gyrus	brain
9	chr6:31783600-31785000	Weak transcription	Brain Hippocampus Middle	brain
10	chr6:31783600-31785000	Weak transcription	Brain Substantia Nigra	brain
11	chr6:31783600-31785000	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr6:31783600-31785000	Weak transcription	Pancreas	Pancrea
13	chr6:31783600-31785000	Weak transcription	Spleen	Spleen
14	chr6:31783600-31785200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr6:31783600-31785200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr6:31783600-31785200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr6:31783600-31785200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:31783600-31785200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr6:31783600-31785200	Weak transcription	Primary B cells from cord blood	blood
20	chr6:31783600-31785200	Weak transcription	Primary T cells from cord blood	blood
21	chr6:31783600-31785200	Weak transcription	Primary hematopoietic stem cells	blood
22	chr6:31783600-31785200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr6:31783600-31785200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr6:31783600-31785200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr6:31783600-31785200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr6:31783600-31785200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr6:31783600-31785200	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr6:31783600-31785200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr6:31783600-31785200	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr6:31783600-31785200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr6:31783600-31785200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr6:31783600-31785200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr6:31783600-31785200	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr6:31783600-31785200	Weak transcription	Aorta	Aorta
35	chr6:31783600-31785200	Weak transcription	Liver	Liver
36	chr6:31783600-31785200	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr6:31783600-31785200	Weak transcription	Colonic Mucosa	Colon
38	chr6:31783600-31785200	Weak transcription	Colon Smooth Muscle	Colon
39	chr6:31783600-31785200	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr6:31783600-31785200	Weak transcription	Fetal Brain Male	brain
41	chr6:31783600-31785200	Weak transcription	Placenta	Placenta
42	chr6:31783600-31785200	Weak transcription	Gastric	stomach
43	chr6:31783600-31785200	Weak transcription	Ovary	ovary
44	chr6:31783600-31785200	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr6:31783600-31785200	Weak transcription	Thymus	Thymus
46	chr6:31783600-31785200	Weak transcription	A549	lung
47	chr6:31783600-31785200	Weak transcription	GM12878-XiMat	blood
48	chr6:31783600-31785200	Weak transcription	HUVEC	blood vessel
49	chr6:31783600-31785200	Weak transcription	NHDF-Ad	bronchial
50	chr6:31783600-31785200	Weak transcription	NHEK	skin

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