Variant report

Variant	rs33966546
Chromosome Location	chr7:150759978-150759979
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	chr7:150754493-150760694	K562	blood:	n/a	n/a
2	MAX	chr7:150759078-150759991	H1-hESC	embryonic stem cell:	n/a	chr7:150759551-150759560 chr7:150759519-150759526 chr7:150759549-150759558 chr7:150759518-150759527 chr7:150759551-150759560 chr7:150759517-150759527 chr7:150759551-150759560 chr7:150759659-150759668 chr7:150759658-150759669 chr7:150759551-150759561
3	TAF1	chr7:150759338-150760311	HepG2	liver:	n/a	n/a
4	TAF1	chr7:150759249-150760330	K562	blood:	n/a	n/a
5	EP300	chr7:150759365-150760258	HepG2	liver:	n/a	n/a
6	SIN3AK20	chr7:150759841-150760135	A549	lung:	n/a	n/a
7	POLR2A	chr7:150759259-150760197	HepG2	liver:	n/a	n/a
8	USF1	chr7:150759227-150760152	HCT-116	colon:	n/a	chr7:150760120-150760136 chr7:150759659-150759668 chr7:150759659-150759668 chr7:150759658-150759667 chr7:150759657-150759670 chr7:150759658-150759669 chr7:150759660-150759669
9	POLR2A	chr7:150754758-150760600	K562	blood:	n/a	n/a
10	POLR2A	chr7:150758843-150760346	A549	lung:	n/a	n/a
11	USF1	chr7:150759280-150760012	K562	blood:	n/a	chr7:150759659-150759668 chr7:150759659-150759668 chr7:150759658-150759667 chr7:150759657-150759670 chr7:150759658-150759669 chr7:150759660-150759669
12	MYC	chr7:150759071-150760043	H1-hESC	embryonic stem cell:	n/a	chr7:150759551-150759560 chr7:150759519-150759526 chr7:150759549-150759558 chr7:150759518-150759527 chr7:150759551-150759560 chr7:150759517-150759527 chr7:150759551-150759560 chr7:150759659-150759668 chr7:150759658-150759669 chr7:150759551-150759561
13	CHD1	chr7:150759727-150760159	H1-hESC	embryonic stem cell:	n/a	chr7:150759971-150759981
14	ZBTB7A	chr7:150756227-150760413	K562	blood:	n/a	chr7:150757231-150757239 chr7:150758070-150758079 chr7:150757085-150757094
15	SP1	chr7:150759359-150760267	HepG2	liver:	n/a	chr7:150759543-150759552 chr7:150759689-150759703 chr7:150759532-150759544 chr7:150759690-150759699 chr7:150759505-150759515 chr7:150759837-150759847 chr7:150760149-150760163 chr7:150759532-150759544 chr7:150759504-150759516 chr7:150759688-150759700 chr7:150759504-150759516 chr7:150759532-150759543 chr7:150759505-150759515 chr7:150759998-150760012 chr7:150759533-150759542
16	MAX	chr7:150759332-150760200	HepG2	liver:	n/a	chr7:150759551-150759560 chr7:150759519-150759526 chr7:150759549-150759558 chr7:150759518-150759527 chr7:150759551-150759560 chr7:150759517-150759527 chr7:150759551-150759560 chr7:150759659-150759668 chr7:150759658-150759669 chr7:150759551-150759561
17	MAX	chr7:150758741-150760286	K562	blood:	n/a	chr7:150759551-150759560 chr7:150759519-150759526 chr7:150759549-150759558 chr7:150759518-150759527 chr7:150759551-150759560 chr7:150759517-150759527 chr7:150759551-150759560 chr7:150759659-150759668 chr7:150759658-150759669 chr7:150759551-150759561
18	YY1	chr7:150759201-150759980	A549	lung:	n/a	n/a
19	SP1	chr7:150759025-150760261	A549	lung:	n/a	chr7:150759543-150759552 chr7:150759689-150759703 chr7:150759532-150759544 chr7:150759690-150759699 chr7:150759505-150759515 chr7:150759837-150759847 chr7:150760149-150760163 chr7:150759532-150759544 chr7:150759504-150759516 chr7:150759688-150759700 chr7:150759504-150759516 chr7:150759320-150759333 chr7:150759532-150759543 chr7:150759505-150759515 chr7:150759998-150760012 chr7:150759533-150759542
20	MAX	chr7:150759012-150760783	HepG2	liver:	n/a	chr7:150759551-150759560 chr7:150759519-150759526 chr7:150759549-150759558 chr7:150759518-150759527 chr7:150759551-150759560 chr7:150759517-150759527 chr7:150759551-150759560 chr7:150759659-150759668 chr7:150759658-150759669 chr7:150759551-150759561
21	POLR2A	chr7:150759876-150759983	ProgFib	skin:	n/a	n/a
22	ZBTB7A	chr7:150758844-150760744	K562	blood:	n/a	n/a
23	MYBL2	chr7:150759235-150760126	HepG2	liver:	n/a	n/a
24	MXI1	chr7:150754410-150760844	IMR90	lung:	n/a	chr7:150759550-150759559 chr7:150759552-150759561 chr7:150760584-150760593 chr7:150759552-150759561
25	MAX	chr7:150758883-150760256	H1-hESC	embryonic stem cell:	n/a	chr7:150759551-150759560 chr7:150759519-150759526 chr7:150759549-150759558 chr7:150759518-150759527 chr7:150759551-150759560 chr7:150759517-150759527 chr7:150759551-150759560 chr7:150759659-150759668 chr7:150759658-150759669 chr7:150759551-150759561
26	MYC	chr7:150759316-150760487	Hela-S3	cervix:	n/a	chr7:150759551-150759560 chr7:150759519-150759526 chr7:150759549-150759558 chr7:150759518-150759527 chr7:150759551-150759560 chr7:150759517-150759527 chr7:150759551-150759560 chr7:150759659-150759668 chr7:150759658-150759669 chr7:150759551-150759561
27	GATA3	chr7:150759578-150760346	MCF-7	breast:	n/a	n/a
28	MYC	chr7:150758762-150760626	K562	blood:	n/a	chr7:150759551-150759560 chr7:150759519-150759526 chr7:150759549-150759558 chr7:150759518-150759527 chr7:150759551-150759560 chr7:150759517-150759527 chr7:150759551-150759560 chr7:150759659-150759668 chr7:150759658-150759669 chr7:150759551-150759561
29	USF1	chr7:150759022-150760110	HCT-116	colon:	n/a	chr7:150759659-150759668 chr7:150759659-150759668 chr7:150759658-150759667 chr7:150759657-150759670 chr7:150759658-150759669 chr7:150759660-150759669
30	MAX	chr7:150759304-150760652	Hela-S3	cervix:	n/a	chr7:150759551-150759560 chr7:150759519-150759526 chr7:150759549-150759558 chr7:150759518-150759527 chr7:150759551-150759560 chr7:150759517-150759527 chr7:150759551-150759560 chr7:150759659-150759668 chr7:150759658-150759669 chr7:150759551-150759561
31	MAX	chr7:150759161-150760660	HepG2	liver:	n/a	chr7:150759551-150759560 chr7:150759519-150759526 chr7:150759549-150759558 chr7:150759518-150759527 chr7:150759551-150759560 chr7:150759517-150759527 chr7:150759551-150759560 chr7:150759659-150759668 chr7:150759658-150759669 chr7:150759551-150759561
32	MAX	chr7:150759145-150760852	MCF-7	breast:	n/a	chr7:150759551-150759560 chr7:150759519-150759526 chr7:150759549-150759558 chr7:150759518-150759527 chr7:150759551-150759560 chr7:150759517-150759527 chr7:150759551-150759560 chr7:150759659-150759668 chr7:150759658-150759669 chr7:150759551-150759561
33	TEAD4	chr7:150759796-150760197	HepG2	liver:	n/a	n/a
34	POLR2A	chr7:150758344-150760685	K562	blood:	n/a	n/a
35	CHD2	chr7:150759038-150760104	K562	blood:	n/a	chr7:150759971-150759981
36	MYC	chr7:150759286-150760031	HepG2	liver:	n/a	chr7:150759551-150759560 chr7:150759519-150759526 chr7:150759549-150759558 chr7:150759518-150759527 chr7:150759551-150759560 chr7:150759517-150759527 chr7:150759551-150759560 chr7:150759659-150759668 chr7:150759658-150759669 chr7:150759551-150759561
37	MXI1	chr7:150759159-150760159	K562	blood:	n/a	chr7:150759550-150759559 chr7:150759552-150759561 chr7:150759552-150759561
38	ZBTB7A	chr7:150759531-150760219	HepG2	liver:	n/a	n/a
39	PBX3	chr7:150759046-150760064	A549	lung:	n/a	n/a
40	MAZ	chr7:150759393-150760665	Hela-S3	cervix:	n/a	chr7:150759551-150759560 chr7:150759519-150759526 chr7:150759549-150759558 chr7:150759518-150759527 chr7:150759551-150759560 chr7:150759517-150759527 chr7:150759551-150759560 chr7:150759659-150759668 chr7:150759658-150759669 chr7:150759551-150759561
41	POLR2A	chr7:150754806-150760313	K562	blood:	n/a	n/a
42	SIN3AK20	chr7:150759471-150760017	A549	lung:	n/a	n/a
43	POLR2A	chr7:150754523-150760219	SK-N-MC	brain:	n/a	n/a
44	ETS1	chr7:150759294-150760727	K562	blood:	n/a	chr7:150759533-150759546 chr7:150760571-150760580 chr7:150760366-150760379 chr7:150759690-150759701
45	EGR1	chr7:150759825-150760307	MCF-7	breast:	n/a	n/a
46	CTBP2	chr7:150759074-150760166	H1-hESC	embryonic stem cell:	n/a	n/a
47	MYBL2	chr7:150759250-150760006	HepG2	liver:	n/a	n/a
48	UBTF	chr7:150758356-150760596	K562	blood:	n/a	n/a
49	NR2F2	chr7:150758136-150760632	K562	blood:	n/a	n/a
50	MAZ	chr7:150759169-150760910	IMR90	lung:	n/a	chr7:150759551-150759560 chr7:150759519-150759526 chr7:150759549-150759558 chr7:150759518-150759527 chr7:150759551-150759560 chr7:150759517-150759527 chr7:150759551-150759560 chr7:150759659-150759668 chr7:150759658-150759669 chr7:150759551-150759561

No.	Distal block	Cell Line	Cell type
1	chr7:150728026..150728575-chr7:150759948..150760471,2	MCF-7	breast:
2	chr6:33166816..33168593-chr7:150759219..150760727,2	MCF-7	breast:
3	chr3:64252018..64254235-chr7:150757748..150760027,2	MCF-7	breast:
4	chr17:56707568..56709230-chr7:150758824..150761309,2	MCF-7	breast:
5	chr7:150759793..150760405-chr7:150784143..150784696,2	MCF-7	breast:

Variant related genes	Relation type
CDK5	TF binding region
ENSG00000202441	Chromatin interaction
ENSG00000204231	Chromatin interaction
ENSG00000133612	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000163637	Chromatin interaction
ENSG00000112473	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10245199	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1549760	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2303929	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2303931	0.80[EUR][1000 genomes]
rs34403003	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs34812229	0.83[AMR][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	esv1821419	chr7:150593315-150974269	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	128 gene(s)	inside rSNPs	diseases
2	nsv1022246	chr7:150619660-150779924	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Enhancers Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	nsv889465	chr7:150640285-150800823	Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
4	nsv1017863	chr7:150643928-150779924	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
5	nsv539197	chr7:150643928-150779924	Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
6	nsv1028645	chr7:150643928-150806534	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases
7	nsv539198	chr7:150643928-150879259	Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
8	nsv526410	chr7:150714812-150775306	Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
9	nsv889476	chr7:150729212-150951819	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	120 gene(s)	inside rSNPs	diseases
10	nsv1031733	chr7:150730999-150790517	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
11	nsv524928	chr7:150731698-150766799	Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
12	nsv889477	chr7:150731698-150837529	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
13	nsv889478	chr7:150732812-150889527	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases
14	nsv831188	chr7:150735204-150912875	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers 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	64 gene(s)	inside rSNPs	diseases
15	nsv889479	chr7:150736382-150785321	Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
16	nsv889480	chr7:150736382-150797581	Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
17	nsv1028023	chr7:150738624-150790517	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
18	nsv465214	chr7:150751590-150822192	Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
19	nsv609012	chr7:150751590-150822192	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
20	nsv609013	chr7:150751590-150832913	Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150757400-150760000	Flanking Active TSS	Rectal Smooth Muscle	rectum
2	chr7:150757400-150760200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr7:150757400-150760200	Flanking Active TSS	Stomach Smooth Muscle	stomach
4	chr7:150757400-150760200	Flanking Active TSS	NH-A	brain
5	chr7:150757400-150760400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:150757600-150760200	Flanking Active TSS	HMEC	breast
7	chr7:150757800-150760200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr7:150757800-150760800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr7:150757800-150760800	Enhancers	Placenta Amnion	Placenta Amnion
10	chr7:150757800-150761600	Weak transcription	Aorta	Aorta
11	chr7:150758000-150760000	Enhancers	Ovary	ovary
12	chr7:150758000-150760800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr7:150758000-150760800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr7:150758000-150760800	Enhancers	Sigmoid Colon	Sigmoid Colon
15	chr7:150758200-150760400	Weak transcription	Fetal Kidney	kidney
16	chr7:150758200-150760800	Enhancers	Adipose Nuclei	Adipose
17	chr7:150758200-150760800	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr7:150758200-150760800	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr7:150758200-150761000	Enhancers	Fetal Muscle Trunk	muscle
20	chr7:150758200-150761200	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr7:150758200-150761600	Weak transcription	Psoas Muscle	Psoas
22	chr7:150758200-150762000	Weak transcription	Primary T cells from cord blood	blood
23	chr7:150758400-150760200	Flanking Active TSS	HSMM	muscle
24	chr7:150758400-150760600	Enhancers	NHDF-Ad	bronchial
25	chr7:150758400-150761600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr7:150758400-150761600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr7:150758400-150761800	Weak transcription	Fetal Brain Female	brain
28	chr7:150758400-150764000	Weak transcription	Primary B cells from cord blood	blood
29	chr7:150758400-150776000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr7:150758600-150760000	Flanking Active TSS	HSMMtube	muscle
31	chr7:150758600-150760600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr7:150758600-150760800	Genic enhancers	Fetal Muscle Leg	muscle
33	chr7:150758600-150761200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr7:150758600-150761600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr7:150758600-150764600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr7:150758600-150766600	Weak transcription	Brain Angular Gyrus	brain
37	chr7:150758800-150760000	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr7:150758800-150760000	Transcr. at gene 5' and 3'	NHLF	lung
39	chr7:150758800-150760200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr7:150758800-150760600	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr7:150758800-150760800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr7:150758800-150761200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr7:150758800-150774600	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr7:150758800-150774800	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr7:150758800-150775800	Strong transcription	Thymus	Thymus
46	chr7:150759000-150760000	Weak transcription	Primary B cells from peripheral blood	blood
47	chr7:150759000-150760000	Strong transcription	Fetal Thymus	thymus
48	chr7:150759000-150760200	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr7:150759000-150760200	Flanking Active TSS	Colonic Mucosa	Colon
50	chr7:150759000-150760200	Genic enhancers	Spleen	Spleen

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links