Variant report

Variant	rs74089060
Chromosome Location	chr12:49740937-49740938
allele	G/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	E2F6	chr12:49740534-49740996	H1-hESC	embryonic stem cell:	n/a	chr12:49740739-49740750 chr12:49740613-49740622
2	MAX	chr12:49740402-49742031	MCF-7	breast:	n/a	n/a
3	GTF2F1	chr12:49740854-49741837	Hela-S3	cervix:	n/a	n/a
4	MAX	chr12:49740385-49742027	ECC-1	luminal epithelium:	n/a	n/a
5	TCF12	chr12:49740213-49742052	ECC-1	luminal epithelium:	n/a	chr12:49741032-49741042
6	CTCF	chr12:49740800-49740950	GM12869	blood:	n/a	n/a
7	KAP1	chr12:49740630-49741894	HEK293	kidney:	n/a	n/a
8	MAX	chr12:49740435-49742080	A549	lung:	n/a	n/a
9	E2F6	chr12:49740549-49741539	K562	blood:	n/a	chr12:49740739-49740750 chr12:49740613-49740622
10	ZBTB7A	chr12:49738646-49742163	ECC-1	luminal epithelium:	n/a	chr12:49739274-49739281 chr12:49741924-49741935 chr12:49741555-49741564
11	KAP1	chr12:49740560-49741698	U2OS	brain:	n/a	n/a
12	CTCF	chr12:49740900-49741050	HCM	heart:	n/a	n/a
13	TCF12	chr12:49740418-49742001	ECC-1	luminal epithelium:	n/a	chr12:49741032-49741042
14	PAX5	chr12:49740922-49741744	GM12892	blood:	n/a	chr12:49741295-49741313 chr12:49741297-49741314 chr12:49741296-49741315
15	CTCF	chr12:49740920-49741070	GM06990	blood:	n/a	n/a
16	CTCF	chr12:49740760-49741010	HRE	kidney:	n/a	n/a
17	UBTF	chr12:49740420-49741077	K562	blood:	n/a	n/a
18	E2F6	chr12:49740400-49741117	K562	blood:	n/a	chr12:49740463-49740473 chr12:49740739-49740750 chr12:49740613-49740622 chr12:49740466-49740476 chr12:49740519-49740529
19	CTCF	chr12:49740860-49741010	GM12871	blood:	n/a	n/a
20	CTCF	chr12:49740920-49741070	HBMEC	blood vessel:	n/a	n/a
21	EGR1	chr12:49739483-49741923	MCF-7	breast:	n/a	chr12:49740466-49740479 chr12:49740522-49740536 chr12:49740007-49740020 chr12:49740612-49740622 chr12:49740520-49740542 chr12:49739746-49739759 chr12:49740608-49740621 chr12:49739998-49740008 chr12:49740466-49740479 chr12:49739743-49739757 chr12:49740526-49740536 chr12:49739747-49739757 chr12:49740608-49740621 chr12:49740525-49740538 chr12:49740524-49740538 chr12:49739747-49739757 chr12:49741709-49741719 chr12:49739746-49739759 chr12:49740799-49740812 chr12:49740007-49740017 chr12:49740608-49740618 chr12:49740526-49740536 chr12:49740526-49740537 chr12:49740608-49740621 chr12:49739976-49739990 chr12:49739745-49739759 chr12:49740461-49740483 chr12:49740006-49740021 chr12:49740609-49740618 chr12:49739746-49739759 chr12:49740607-49740622 chr12:49739747-49739756 chr12:49740607-49740621 chr12:49740525-49740538 chr12:49740613-49740623 chr12:49740467-49740476 chr12:49740466-49740479 chr12:49740466-49740476 chr12:49740608-49740621 chr12:49740004-49740018 chr12:49740526-49740537 chr12:49739747-49739758 chr12:49740525-49740538 chr12:49740526-49740535
22	EGR1	chr12:49740153-49740973	HCT-116	colon:	n/a	chr12:49740466-49740479 chr12:49740522-49740536 chr12:49740612-49740622 chr12:49740520-49740542 chr12:49740608-49740621 chr12:49740466-49740479 chr12:49740526-49740536 chr12:49740608-49740621 chr12:49740525-49740538 chr12:49740524-49740538 chr12:49740799-49740812 chr12:49740608-49740618 chr12:49740526-49740536 chr12:49740526-49740537 chr12:49740608-49740621 chr12:49740461-49740483 chr12:49740609-49740618 chr12:49740607-49740622 chr12:49740607-49740621 chr12:49740525-49740538 chr12:49740613-49740623 chr12:49740467-49740476 chr12:49740466-49740479 chr12:49740466-49740476 chr12:49740608-49740621 chr12:49740526-49740537 chr12:49740525-49740538 chr12:49740526-49740535
23	HDAC2	chr12:49740223-49742034	MCF-7	breast:	n/a	n/a
24	SMC3	chr12:49740372-49742164	SK-N-SH	brain:	n/a	chr12:49741556-49741570 chr12:49741556-49741566 chr12:49741019-49741027
25	MAX	chr12:49740347-49741727	K562	blood:	n/a	n/a
26	MAZ	chr12:49740407-49741813	K562	blood:	n/a	n/a
27	SUZ12	chr12:49740724-49741567	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr12:49740404-49742833	A549	lung:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49740510-49740523 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
29	HA-E2F1	chr12:49740350-49740954	MCF-7	breast:	n/a	chr12:49740463-49740473 chr12:49740613-49740622 chr12:49740466-49740476 chr12:49740519-49740529
30	CTBP2	chr12:49739324-49741267	H1-hESC	embryonic stem cell:	n/a	n/a
31	EGR1	chr12:49740235-49740938	HCT-116	colon:	n/a	chr12:49740466-49740479 chr12:49740522-49740536 chr12:49740612-49740622 chr12:49740520-49740542 chr12:49740608-49740621 chr12:49740466-49740479 chr12:49740526-49740536 chr12:49740608-49740621 chr12:49740525-49740538 chr12:49740524-49740538 chr12:49740799-49740812 chr12:49740608-49740618 chr12:49740526-49740536 chr12:49740526-49740537 chr12:49740608-49740621 chr12:49740461-49740483 chr12:49740609-49740618 chr12:49740607-49740622 chr12:49740607-49740621 chr12:49740525-49740538 chr12:49740613-49740623 chr12:49740467-49740476 chr12:49740466-49740479 chr12:49740466-49740476 chr12:49740608-49740621 chr12:49740526-49740537 chr12:49740525-49740538 chr12:49740526-49740535
32	PML	chr12:49740850-49741569	GM12878	blood:	n/a	n/a
33	CTCF	chr12:49740900-49741050	GM12875	blood:	n/a	n/a
34	NFIC	chr12:49740284-49741942	ECC-1	luminal epithelium:	n/a	n/a
35	POLR2A	chr12:49739596-49741075	H1-neurons	neurons:	n/a	n/a
36	CBX3	chr12:49740645-49741094	K562	blood:	n/a	n/a
37	SMARCB1	chr12:49740882-49741985	Hela-S3	cervix:	n/a	n/a
38	MAX	chr12:49740932-49741114	K562	blood:	n/a	n/a
39	ZBTB7A	chr12:49738673-49741889	ECC-1	luminal epithelium:	n/a	chr12:49739274-49739281 chr12:49741555-49741564
40	SETDB1	chr12:49740710-49741596	U2OS	brain:	n/a	chr12:49741254-49741278
41	SUZ12	chr12:49738478-49741665	NT2-D1	testis:	n/a	n/a
42	E2F6	chr12:49740567-49741222	H1-hESC	embryonic stem cell:	n/a	chr12:49740739-49740750 chr12:49740613-49740622
43	RCOR1	chr12:49740770-49740984	HepG2	liver:	n/a	n/a
44	MAX	chr12:49740356-49742248	A549	lung:	n/a	n/a
45	MAX	chr12:49740433-49741975	HepG2	liver:	n/a	n/a
46	ELF1	chr12:49740235-49741766	GM12878	blood:	n/a	chr12:49740521-49740530 chr12:49740514-49740526 chr12:49740513-49740525 chr12:49740517-49740529 chr12:49740464-49740476 chr12:49740484-49740496 chr12:49741594-49741606 chr12:49741549-49741558
47	E2F6	chr12:49740428-49741938	A549	lung:	n/a	chr12:49740463-49740473 chr12:49741671-49741683 chr12:49740739-49740750 chr12:49740613-49740622 chr12:49740466-49740476 chr12:49740519-49740529
48	EGR1	chr12:49740150-49741821	MCF-7	breast:	n/a	chr12:49740466-49740479 chr12:49740522-49740536 chr12:49740612-49740622 chr12:49740520-49740542 chr12:49740608-49740621 chr12:49740466-49740479 chr12:49740526-49740536 chr12:49740608-49740621 chr12:49740525-49740538 chr12:49740524-49740538 chr12:49741709-49741719 chr12:49740799-49740812 chr12:49740608-49740618 chr12:49740526-49740536 chr12:49740526-49740537 chr12:49740608-49740621 chr12:49740461-49740483 chr12:49740609-49740618 chr12:49740607-49740622 chr12:49740607-49740621 chr12:49740525-49740538 chr12:49740613-49740623 chr12:49740467-49740476 chr12:49740466-49740479 chr12:49740466-49740476 chr12:49740608-49740621 chr12:49740526-49740537 chr12:49740525-49740538 chr12:49740526-49740535
49	POLR2A	chr12:49740556-49742071	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:49740516-49742057	SK-N-SH	brain:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:49740910-49740960	CMK	blood:	n/a
2	chr12:49740910-49740960	HEEpiC	esophagus:	n/a
3	chr12:49740910-49740960	HNPCEpiC	eye:	n/a
4	chr12:49740910-49740960	NT2-D1	testis:	n/a
5	chr12:49740910-49740960	A549	lung:	n/a
6	chr12:49740910-49740960	HAEpiC	amniotic membrane:	n/a
7	chr12:49740910-49740960	AG04449	skin:	fetal
8	chr12:49740910-49740960	GM06990	blood:	n/a
9	chr12:49740910-49740960	GM12892	blood:	n/a
10	chr12:49740910-49740960	NHDF-neo	bronchial:	n/a
11	chr12:49740910-49740960	Caco-2	colon:	n/a
12	chr12:49740910-49740960	GM12891	blood:	n/a
13	chr12:49740910-49740960	AG09319	gingival:	n/a
14	chr12:49740910-49740960	HMEC	breast:	n/a
15	chr12:49740910-49740960	NHBE	bronchial:	n/a
16	chr12:49740910-49740960	SAEC	small airway:	n/a
17	chr12:49740910-49740960	ProgFib	skin:	n/a
18	chr12:49740910-49740960	HUVEC	blood vessel:	n/a
19	chr12:49740910-49740960	SK-N-SH	brain:	n/a
20	chr12:49740910-49740960	H1-hESC	embryonic stem cell:	embryo
21	chr12:49740910-49740960	SKMC	muscle:	n/a
22	chr12:49740910-49740960	NH-A	brain:	n/a
23	chr12:49740910-49740960	HCT-116	colon:	n/a
24	chr12:49740910-49740960	HEK293	kidney:	embryo
25	chr12:49740910-49740960	HCM	heart:	n/a
26	chr12:49740910-49740960	PANC-1	pancreas:	n/a
27	chr12:49740910-49740960	Jurkat	blood:	n/a
28	chr12:49740910-49740960	RPTEC	kidney:	n/a
29	chr12:49740910-49740960	HIPEpiC	eye:	n/a
30	chr12:49740910-49740960	HRCEpiC	kidney:	n/a
31	chr12:49740910-49740960	PrEC	prostate:	n/a
32	chr12:49740910-49740960	SK-N-MC	brain:	n/a
33	chr12:49740910-49740960	GM12878	blood:	n/a
34	chr12:49740910-49740960	BJ	skin:	n/a
35	chr12:49740910-49740960	ECC-1	luminal epithelium:	n/a
36	chr12:49740910-49740960	Hepatocyte	liver:	n/a
37	chr12:49740910-49740960	AG04450	lung:	fetal
38	chr12:49740910-49740960	GM19239	blood:	n/a
39	chr12:49740910-49740960	T-47D	breast:	n/a
40	chr12:49740910-49740960	BE2_C	brain:	n/a
41	chr12:49740910-49740960	U87	brain:	n/a
42	chr12:49740910-49740960	MCF10A-Er-Src	breast:	n/a
43	chr12:49740910-49740960	HPAEpiC	pulmonary alveolar:	n/a
44	chr12:49740910-49740960	Hela-S3	cervix:	n/a
45	chr12:49740910-49740960	ovcar-3	ovarian:	n/a
46	chr12:49740910-49740960	PFSK-1	brain:	n/a
47	chr12:49740910-49740960	NB4	blood:	n/a
48	chr12:49740910-49740960	HL-60	blood:	n/a
49	chr12:49740910-49740960	LNCaP	prostate:	n/a
50	chr12:49740910-49740960	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:49739423..49741666-chr12:49907974..49910735,2	MCF-7	breast:
2	chr12:49656587..49660636-chr12:49733539..49743833,13	K562	blood:
3	chr12:49740832..49741606-chr12:49942595..49943430,2	K562	blood:
4	chr12:49739131..49745064-chr12:49758784..49762517,10	MCF-7	breast:
5	chr12:49683076..49686072-chr12:49740867..49742928,2	MCF-7	breast:
6	chr12:49657182..49662198-chr12:49738070..49742868,13	MCF-7	breast:
7	chr12:49740569..49744952-chr12:49759719..49761508,3	K562	blood:
8	chr12:49740075..49745225-chr12:49756992..49761732,8	K562	blood:
9	chr12:49740266..49744152-chr12:49960185..49963713,4	MCF-7	breast:
10	chr12:49715312..49722303-chr12:49739075..49744198,13	MCF-7	breast:
11	chr12:49740264..49744957-chr12:49759411..49762039,7	MCF-7	breast:
12	chr12:49655321..49661148-chr12:49729487..49743115,26	K562	blood:
13	chr12:49656742..49663815-chr12:49736558..49745017,19	MCF-7	breast:

Variant related genes	Relation type
DNAJC22	TF binding region
DNAJC22	CpG island
ENSG00000135451	Chromatin interaction
ENSG00000187778	Chromatin interaction
ENSG00000123352	Chromatin interaction
ENSG00000258101	Chromatin interaction
ENSG00000110844	Chromatin interaction
ENSG00000167553	Chromatin interaction
ENSG00000258334	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11830820	1.00[AMR][1000 genomes]
rs11836976	1.00[AMR][1000 genomes]
rs17853062	1.00[AMR][1000 genomes]
rs56005192	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56014465	1.00[AMR][1000 genomes]
rs56140046	1.00[AMR][1000 genomes]
rs56330550	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57546911	1.00[AMR][1000 genomes]
rs58557116	1.00[AMR][1000 genomes]
rs59493874	1.00[AMR][1000 genomes]
rs60712360	1.00[AMR][1000 genomes]
rs60865902	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61110708	1.00[AMR][1000 genomes]
rs7296117	1.00[AMR][1000 genomes]
rs7299056	1.00[AMR][1000 genomes]
rs7309243	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74089008	1.00[AMR][1000 genomes]
rs74089010	1.00[AMR][1000 genomes]
rs74089028	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74089030	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74089031	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74089561	1.00[AMR][1000 genomes]
rs74089565	1.00[AMR][1000 genomes]
rs74091029	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051161	chr12:49314550-49828473	Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
2	nsv541489	chr12:49314550-49828473	Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
3	nsv1036452	chr12:49376285-49867760	Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	315 gene(s)	inside rSNPs	diseases
4	nsv428801	chr12:49536659-49744884	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
5	nsv1042122	chr12:49678529-49823168	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
6	nsv1039176	chr12:49678529-49832618	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
7	nsv899068	chr12:49714103-49924637	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
8	nsv832405	chr12:49720279-49910862	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:49738600-49741200	Bivalent Enhancer	Fetal Brain Male	brain
2	chr12:49738800-49741000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
3	chr12:49738800-49741400	Bivalent Enhancer	Fetal Thymus	thymus
4	chr12:49738800-49741800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
5	chr12:49738800-49742000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
6	chr12:49738800-49742000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
7	chr12:49738800-49742000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
8	chr12:49739000-49741200	Bivalent Enhancer	Small Intestine	intestine
9	chr12:49739000-49741400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr12:49739000-49741800	Active TSS	Aorta	Aorta
11	chr12:49739000-49742000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr12:49739000-49742000	Enhancers	Lung	lung
13	chr12:49739000-49742200	Active TSS	Pancreatic Islets	Pancreatic Islet
14	chr12:49739200-49742000	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
15	chr12:49739200-49742200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
16	chr12:49739400-49741000	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr12:49739400-49741000	Flanking Bivalent TSS/Enh	NH-A	brain
18	chr12:49739400-49741200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
19	chr12:49739400-49741200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
20	chr12:49739400-49741200	Flanking Active TSS	Ovary	ovary
21	chr12:49739400-49741200	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
22	chr12:49739400-49741400	Flanking Bivalent TSS/Enh	Muscle Satellite Cultured Cells	--
23	chr12:49739400-49741400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr12:49739400-49741400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr12:49739400-49741400	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr12:49739400-49741600	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
27	chr12:49739400-49741600	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr12:49739400-49741800	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
29	chr12:49739400-49741800	Flanking Bivalent TSS/Enh	Primary T helper 17 cells PMA-I stimulated	--
30	chr12:49739400-49741800	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
31	chr12:49739400-49741800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr12:49739400-49741800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr12:49739400-49741800	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
34	chr12:49739400-49742000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
35	chr12:49739400-49742000	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
36	chr12:49739400-49742000	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
37	chr12:49739400-49742000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
38	chr12:49739400-49742200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr12:49739600-49741200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr12:49739600-49741400	Enhancers	Gastric	stomach
41	chr12:49739600-49742400	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
42	chr12:49739800-49741000	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr12:49739800-49741600	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:49740000-49741000	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
45	chr12:49740000-49741200	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr12:49740000-49741200	Bivalent Enhancer	Fetal Lung	lung
47	chr12:49740000-49741600	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr12:49740000-49741600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
49	chr12:49740200-49741000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
50	chr12:49740200-49741000	Bivalent/Poised TSS	Psoas Muscle	Psoas

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