Variant report

Variant	rs73663033
Chromosome Location	chr8:11724738-11724739
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	POLR2A	chr8:11724697-11725899	K562	blood:	n/a	n/a
2	STAT5A	chr8:11724655-11725141	GM12878	blood:	n/a	chr8:11724890-11724901
3	ELF1	chr8:11724573-11724912	K562	blood:	n/a	chr8:11724894-11724907
4	EBF1	chr8:11724553-11724941	GM12878	blood:	n/a	chr8:11724720-11724731 chr8:11724744-11724755
5	SPI1	chr8:11724670-11725157	GM12891	blood:	n/a	n/a
6	MAX	chr8:11724612-11725859	K562	blood:	n/a	chr8:11724739-11724749
7	ELF1	chr8:11724287-11726193	GM12878	blood:	n/a	chr8:11725974-11725983 chr8:11724894-11724907 chr8:11724294-11724307
8	ATF2	chr8:11724597-11725205	GM12878	blood:	n/a	n/a
9	REST	chr8:11724477-11725872	H1-neurons	neurons:	n/a	chr8:11724505-11724512 chr8:11724708-11724721 chr8:11725604-11725617 chr8:11725182-11725195
10	ELF1	chr8:11724701-11725090	K562	blood:	n/a	chr8:11724894-11724907
11	EP300	chr8:11724717-11725112	GM12878	blood:	n/a	chr8:11724892-11724906
12	POLR2A	chr8:11723622-11725666	PBDE	blood:	n/a	n/a
13	SPI1	chr8:11724612-11725154	GM12891	blood:	n/a	n/a
14	POLR2A	chr8:11723723-11726721	HepG2	liver:	n/a	n/a
15	SMARCB1	chr8:11723731-11725527	Hela-S3	cervix:	n/a	chr8:11724117-11724126
16	EBF1	chr8:11724555-11724841	GM12878	blood:	n/a	chr8:11724720-11724731 chr8:11724744-11724755
17	CCNT2	chr8:11724104-11726088	K562	blood:	n/a	chr8:11726021-11726030
18	TEAD4	chr8:11724686-11725098	K562	blood:	n/a	n/a
19	CHD1	chr8:11723365-11726352	IMR90	lung:	n/a	n/a
20	SIN3AK20	chr8:11724679-11725088	PFSK-1	brain:	n/a	n/a
21	JUND	chr8:11724729-11725002	K562	blood:	n/a	n/a
22	UBTF	chr8:11723853-11725745	K562	blood:	n/a	n/a
23	MAZ	chr8:11724686-11725024	GM12878	blood:	n/a	chr8:11724739-11724749
24	SIN3A	chr8:11724669-11725645	H1-hESC	embryonic stem cell:	n/a	chr8:11725278-11725286 chr8:11725119-11725128 chr8:11725548-11725559 chr8:11725604-11725617
25	ZBTB7A	chr8:11724554-11726351	ECC-1	luminal epithelium:	n/a	n/a
26	POLR2A	chr8:11723577-11726448	MCF10A-Er-Src	breast:	n/a	n/a
27	MTA3	chr8:11724600-11725323	GM12878	blood:	n/a	n/a
28	POLR2A	chr8:11724386-11725833	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr8:11724708-11726083	HUVEC	blood vessel:	n/a	n/a
30	EBF1	chr8:11724563-11724988	GM12878	blood:	n/a	chr8:11724720-11724731 chr8:11724744-11724755
31	POLR2A	chr8:11724346-11725758	IMR90	lung:	n/a	n/a
32	CBX3	chr8:11724617-11725011	K562	blood:	n/a	n/a
33	POLR2A	chr8:11723707-11725173	K562	blood:	n/a	n/a
34	ZBTB7A	chr8:11724458-11726350	ECC-1	luminal epithelium:	n/a	n/a
35	FOXM1	chr8:11724704-11725212	GM12878	blood:	n/a	n/a
36	ZMIZ1	chr8:11724726-11724864	K562	blood:	n/a	n/a
37	POLR2A	chr8:11724676-11725194	HUVEC	blood vessel:	n/a	n/a
38	POLR2A	chr8:11724681-11726197	SK-N-MC	brain:	n/a	n/a
39	POLR2A	chr8:11724552-11725174	H1-neurons	neurons:	n/a	n/a
40	SPI1	chr8:11724462-11725365	GM12878	blood:	n/a	chr8:11725254-11725267
41	PAX5	chr8:11724733-11724996	GM12878	blood:	n/a	chr8:11724892-11724901 chr8:11724895-11724904
42	ZBTB7A	chr8:11724416-11726318	K562	blood:	n/a	n/a
43	RCOR1	chr8:11724724-11725211	GM12878	blood:	n/a	n/a
44	POLR2A	chr8:11724695-11725205	HUVEC	blood vessel:	n/a	n/a
45	HMGN3	chr8:11724674-11726120	K562	blood:	n/a	n/a
46	POLR2A	chr8:11717595-11726429	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr8:11724700-11725244	PFSK-1	brain:	n/a	n/a
48	POLR2A	chr8:11724659-11725886	HUVEC	blood vessel:	n/a	n/a
49	POLR2A	chr8:11723599-11726575	K562	blood:	n/a	n/a
50	MAZ	chr8:11724271-11726555	IMR90	lung:	n/a	chr8:11724739-11724749 chr8:11725956-11725966 chr8:11726080-11726090

No.	Distal block	Cell Line	Cell type
1	chr8:11625866..11628884-chr8:11724599..11727626,3	MCF-7	breast:
2	chr8:11626986..11628635-chr8:11724070..11726191,2	K562	blood:
3	chr8:11724192..11726313-chr8:11753136..11754724,2	MCF-7	breast:
4	chr8:11706290..11708186-chr8:11724044..11726922,3	MCF-7	breast:
5	chr8:11658864..11661745-chr8:11724576..11726431,3	MCF-7	breast:
6	chr8:11701711..11703998-chr8:11723479..11725596,2	K562	blood:
7	chr8:11659426..11661474-chr8:11724613..11726870,3	MCF-7	breast:
8	chr8:11710836..11712408-chr8:11724380..11726355,2	MCF-7	breast:
9	chr8:11701610..11705224-chr8:11724505..11726759,3	MCF-7	breast:
10	chr8:11678607..11680636-chr8:11724388..11726584,2	MCF-7	breast:
11	chr8:11708512..11715317-chr8:11723234..11727095,9	MCF-7	breast:
12	chr8:11695946..11697771-chr8:11722616..11724742,2	MCF-7	breast:

Variant related genes	Relation type
CTSB	TF binding region
ENSG00000269899	Chromatin interaction
ENSG00000154328	Chromatin interaction
ENSG00000164733	Chromatin interaction
ENSG00000079459	Chromatin interaction
ENSG00000255144	Chromatin interaction
ENSG00000255046	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10089013	1.00[AMR][1000 genomes]
rs10093429	1.00[AMR][1000 genomes]
rs13361	1.00[AMR][1000 genomes]
rs2446	1.00[AMR][1000 genomes]
rs28380721	1.00[AMR][1000 genomes]
rs28391704	1.00[AMR][1000 genomes]
rs28481870	1.00[AMR][1000 genomes]
rs28615101	1.00[AMR][1000 genomes]
rs28827548	1.00[AMR][1000 genomes]
rs3189016	1.00[AMR][1000 genomes]
rs55774923	1.00[AMR][1000 genomes]
rs55865186	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57575026	1.00[AMR][1000 genomes]
rs58057768	1.00[AMR][1000 genomes]
rs58922796	1.00[AMR][1000 genomes]
rs59270740	1.00[AMR][1000 genomes]
rs60079257	1.00[AMR][1000 genomes]
rs60409649	1.00[AMR][1000 genomes]
rs60729363	1.00[AMR][1000 genomes]
rs61394300	1.00[AMR][1000 genomes]
rs73543167	1.00[AMR][1000 genomes]
rs73663010	1.00[AMR][1000 genomes]
rs73663017	1.00[AMR][1000 genomes]
rs73663018	1.00[AMR][1000 genomes]
rs73663020	1.00[AMR][1000 genomes]
rs73663036	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv1018978	chr8:11438267-11858466	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv917963	chr8:11540723-11751798	Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv1027378	chr8:11541739-11858466	Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv1028229	chr8:11575762-11805961	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv539475	chr8:11575762-11805961	Flanking Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv428514	chr8:11580381-11765706	Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
8	nsv1034014	chr8:11602337-11858466	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
9	nsv890361	chr8:11625808-11755513	Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
10	nsv890362	chr8:11625808-11771089	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
11	nsv1034132	chr8:11657033-12198242	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
12	nsv890365	chr8:11666451-11735641	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
13	nsv890366	chr8:11666451-11900847	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
14	nsv1031158	chr8:11666558-11759064	Bivalent Enhancer Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
15	nsv539477	chr8:11666558-11759064	Enhancers Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
16	nsv1018042	chr8:11667496-11882385	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
17	nsv890367	chr8:11668153-11793529	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS 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	11 gene(s)	inside rSNPs	diseases
18	nsv890369	chr8:11671041-11840011	Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
19	nsv1016952	chr8:11679271-11849955	Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
20	nsv1029093	chr8:11679271-11858466	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
21	nsv539478	chr8:11679271-11858466	Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Flanking Active 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	15 gene(s)	inside rSNPs	diseases
22	nsv1017334	chr8:11688534-11732949	Enhancers Active TSS Genic 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	9 gene(s)	inside rSNPs	diseases
23	nsv539479	chr8:11688534-11732949	Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
24	nsv1019738	chr8:11696393-11732949	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
25	nsv539480	chr8:11696393-11732949	Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
26	nsv1031972	chr8:11696393-11805961	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
27	nsv539481	chr8:11696393-11805961	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
28	esv34042	chr8:11698337-11726817	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
29	nsv610293	chr8:11698747-11929734	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
30	nsv516685	chr8:11698747-12570199	Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	74 gene(s)	inside rSNPs	diseases
31	esv3409280	chr8:11724368-11727116	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	9 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	chr8:11721200-11724800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr8:11721600-11724800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
3	chr8:11721800-11725000	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
4	chr8:11722600-11724800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
5	chr8:11722800-11724800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
6	chr8:11723000-11725000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
7	chr8:11723000-11726000	Active TSS	Liver	Liver
8	chr8:11723400-11724800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
9	chr8:11723400-11726200	Active TSS	Fetal Kidney	kidney
10	chr8:11723400-11726400	Active TSS	Brain Substantia Nigra	brain
11	chr8:11723600-11724800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr8:11723600-11724800	Flanking Active TSS	Brain Angular Gyrus	brain
13	chr8:11723600-11724800	Flanking Active TSS	Fetal Muscle Leg	muscle
14	chr8:11723600-11724800	Flanking Active TSS	Placenta	Placenta
15	chr8:11723600-11724800	Flanking Active TSS	Fetal Thymus	thymus
16	chr8:11723600-11724800	Flanking Active TSS	Stomach Smooth Muscle	stomach
17	chr8:11723600-11724800	Flanking Active TSS	Dnd41	blood
18	chr8:11723600-11725000	Flanking Active TSS	Adipose Nuclei	Adipose
19	chr8:11723600-11725000	Flanking Active TSS	Brain Hippocampus Middle	brain
20	chr8:11723600-11725000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
21	chr8:11723600-11725000	Flanking Active TSS	Hela-S3	cervix
22	chr8:11723600-11725200	Flanking Active TSS	Primary B cells from cord blood	blood
23	chr8:11723600-11725200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
24	chr8:11723600-11725200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr8:11723600-11726600	Active TSS	Fetal Brain Female	brain
26	chr8:11723800-11724800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr8:11723800-11724800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr8:11723800-11724800	Flanking Active TSS	Colonic Mucosa	Colon
29	chr8:11723800-11724800	Flanking Active TSS	Pancreas	Pancrea
30	chr8:11723800-11724800	Flanking Active TSS	Placenta Amnion	Placenta Amnion
31	chr8:11723800-11724800	Flanking Active TSS	Stomach Mucosa	stomach
32	chr8:11723800-11725800	Active TSS	Thymus	Thymus
33	chr8:11723800-11726000	Active TSS	Small Intestine	intestine
34	chr8:11723800-11726000	Active TSS	HSMMtube	muscle
35	chr8:11724000-11725200	Bivalent/Poised TSS	HepG2	liver
36	chr8:11724000-11726000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr8:11724000-11726000	Active TSS	NHDF-Ad	bronchial
38	chr8:11724000-11726200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr8:11724000-11726200	Active TSS	Brain Anterior Caudate	brain
40	chr8:11724000-11726200	Active TSS	Brain Cingulate Gyrus	brain
41	chr8:11724000-11726200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
42	chr8:11724000-11726200	Active TSS	Duodenum Smooth Muscle	Duodenum
43	chr8:11724000-11726400	Active TSS	Fetal Intestine Large	intestine
44	chr8:11724000-11726400	Active TSS	Psoas Muscle	Psoas
45	chr8:11724000-11727400	Active TSS	Rectal Smooth Muscle	rectum
46	chr8:11724200-11724800	Flanking Active TSS	Primary hematopoietic stem cells	blood
47	chr8:11724200-11724800	Flanking Active TSS	Brain Germinal Matrix	brain
48	chr8:11724200-11724800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
49	chr8:11724200-11724800	Flanking Active TSS	Fetal Heart	heart
50	chr8:11724200-11725000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links