Variant report

Variant	rs2289443
Chromosome Location	chr4:75023709-75023710
allele	A/G
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	SIN3AK20	chr4:75023176-75024249	HCT-116	colon:	n/a	n/a
2	YY1	chr4:75023484-75024359	GM12878	blood:	n/a	chr4:75023644-75023658 chr4:75024007-75024021 chr4:75023570-75023584 chr4:75024006-75024020 chr4:75023646-75023655 chr4:75024151-75024165 chr4:75024016-75024030
3	TCF12	chr4:75023349-75024066	ECC-1	luminal epithelium:	n/a	n/a
4	BHLHE40	chr4:75023367-75024606	GM12878	blood:	n/a	chr4:75023644-75023660 chr4:75024010-75024026 chr4:75024026-75024042 chr4:75024005-75024021
5	POLR2A	chr4:75023261-75024021	K562	blood:	n/a	n/a
6	BCLAF1	chr4:75023212-75023918	K562	blood:	n/a	n/a
7	MYC	chr4:75023345-75024393	K562	blood:	n/a	chr4:75024298-75024309 chr4:75024298-75024308 chr4:75024299-75024309 chr4:75024297-75024310 chr4:75024299-75024306 chr4:75024295-75024310 chr4:75024297-75024307 chr4:75024300-75024309 chr4:75024297-75024310 chr4:75024297-75024312 chr4:75024299-75024308 chr4:75024298-75024309 chr4:75024298-75024307 chr4:75024298-75024309
8	MYBL2	chr4:75023272-75023986	HepG2	liver:	n/a	n/a
9	YY1	chr4:75023625-75024062	GM12892	blood:	n/a	chr4:75023644-75023658 chr4:75024007-75024021 chr4:75024006-75024020 chr4:75023646-75023655 chr4:75024016-75024030
10	E2F6	chr4:75023402-75024378	K562	blood:	n/a	chr4:75023646-75023655 chr4:75023641-75023651
11	ATF3	chr4:75023411-75023934	A549	lung:	n/a	chr4:75023646-75023655
12	TAF1	chr4:75023397-75024034	SK-N-SH	brain:	n/a	n/a
13	SP1	chr4:75023374-75024041	K562	blood:	n/a	chr4:75023646-75023655 chr4:75023773-75023785 chr4:75023644-75023656 chr4:75023645-75023655 chr4:75023645-75023655 chr4:75023645-75023659 chr4:75023773-75023785 chr4:75023645-75023654 chr4:75023770-75023784 chr4:75023644-75023656 chr4:75023645-75023654
14	MAX	chr4:75023292-75024431	HepG2	liver:	n/a	chr4:75024298-75024309 chr4:75024298-75024308 chr4:75024299-75024309 chr4:75024297-75024310 chr4:75024299-75024306 chr4:75024295-75024310 chr4:75024297-75024307 chr4:75024300-75024309 chr4:75024297-75024310 chr4:75024297-75024312 chr4:75024299-75024308 chr4:75024298-75024309 chr4:75024298-75024307 chr4:75024298-75024309
15	FOS	chr4:75022848-75023827	HUVEC	blood vessel:	n/a	n/a
16	MYC	chr4:75023366-75023916	MCF10A-Er-Src	breast:	n/a	n/a
17	HDAC2	chr4:75023507-75023891	K562	blood:	n/a	n/a
18	MXI1	chr4:75023021-75023940	K562	blood:	n/a	n/a
19	NR2F2	chr4:75023366-75024019	K562	blood:	n/a	n/a
20	POLR2A	chr4:75022946-75024297	K562	blood:	n/a	n/a
21	POLR2A	chr4:75022991-75025136	PBDE	blood:	n/a	n/a
22	CHD1	chr4:75023604-75024854	GM12878	blood:	n/a	n/a
23	MAX	chr4:75023358-75024474	HUVEC	blood vessel:	n/a	chr4:75024298-75024309 chr4:75024298-75024308 chr4:75024299-75024309 chr4:75024297-75024310 chr4:75024299-75024306 chr4:75024295-75024310 chr4:75024297-75024307 chr4:75024300-75024309 chr4:75024297-75024310 chr4:75024297-75024312 chr4:75024299-75024308 chr4:75024298-75024309 chr4:75024298-75024307 chr4:75024298-75024309
24	TEAD4	chr4:75023354-75024064	ECC-1	luminal epithelium:	n/a	n/a
25	TAF7	chr4:75023307-75024048	H1-hESC	embryonic stem cell:	n/a	n/a
26	TCF7L2	chr4:75023389-75023863	PANC-1	pancreas:	n/a	n/a
27	HDAC2	chr4:75023398-75024136	H1-hESC	embryonic stem cell:	n/a	n/a
28	RUNX3	chr4:75023409-75024383	GM12878	blood:	n/a	n/a
29	POLR2A	chr4:75023432-75024344	GM12891	blood:	n/a	n/a
30	POLR2A	chr4:75023343-75024299	NB4	blood:	n/a	n/a
31	ZBTB7A	chr4:75023516-75024170	K562	blood:	n/a	n/a
32	EP300	chr4:75022852-75023944	K562	blood:	n/a	n/a
33	SMARCB1	chr4:75023477-75024309	Hela-S3	cervix:	n/a	n/a
34	REST	chr4:75022921-75024668	H1-neurons	neurons:	n/a	chr4:75023676-75023696 chr4:75024016-75024026 chr4:75023771-75023784 chr4:75023682-75023696 chr4:75023645-75023658
35	GABPA	chr4:75023336-75024201	K562	blood:	n/a	chr4:75024010-75024019 chr4:75023646-75023655
36	POLR2A	chr4:75023430-75024385	GM12892	blood:	n/a	n/a
37	CREB1	chr4:75023309-75024124	HepG2	liver:	n/a	n/a
38	BCL3	chr4:75023580-75024083	GM12878	blood:	n/a	chr4:75024006-75024019 chr4:75024013-75024026
39	TBL1XR1	chr4:75023543-75023993	K562	blood:	n/a	n/a
40	MAX	chr4:75023347-75024435	H1-hESC	embryonic stem cell:	n/a	chr4:75024298-75024309 chr4:75024298-75024308 chr4:75024299-75024309 chr4:75024297-75024310 chr4:75024299-75024306 chr4:75024295-75024310 chr4:75024297-75024307 chr4:75024300-75024309 chr4:75024297-75024310 chr4:75024297-75024312 chr4:75024299-75024308 chr4:75024298-75024309 chr4:75024298-75024307 chr4:75024298-75024309
41	FOSL2	chr4:75023326-75023975	HepG2	liver:	n/a	n/a
42	HCFC1	chr4:75022751-75025210	Hela-S3	cervix:	n/a	n/a
43	MAX	chr4:75023314-75024474	H1-hESC	embryonic stem cell:	n/a	chr4:75024298-75024309 chr4:75024298-75024308 chr4:75024299-75024309 chr4:75024297-75024310 chr4:75024299-75024306 chr4:75024295-75024310 chr4:75024297-75024307 chr4:75024300-75024309 chr4:75024297-75024310 chr4:75024297-75024312 chr4:75024299-75024308 chr4:75024298-75024309 chr4:75024298-75024307 chr4:75024298-75024309
44	RELA	chr4:75023298-75024328	GM15510	blood:	n/a	n/a
45	USF1	chr4:75023544-75023880	A549	lung:	n/a	chr4:75023644-75023660
46	NFIC	chr4:75023237-75024109	ECC-1	luminal epithelium:	n/a	n/a
47	POLR2A	chr4:75023459-75024012	GM12891	blood:	n/a	n/a
48	POLR2A	chr4:75022866-75024826	GM12891	blood:	n/a	n/a
49	POLR2A	chr4:75023316-75024013	SK-N-MC	brain:	n/a	n/a
50	POLR2A	chr4:75023016-75024310	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:75023664-75023714	AG04450	lung:	fetal
2	chr4:75023664-75023714	GM06990	blood:	n/a
3	chr4:75023664-75023714	H1-hESC	embryonic stem cell:	embryo
4	chr4:75023664-75023714	T-47D	breast:	n/a
5	chr4:75023664-75023714	Jurkat	blood:	n/a
6	chr4:75023664-75023714	ECC-1	luminal epithelium:	n/a
7	chr4:75023664-75023714	NHDF-neo	bronchial:	n/a
8	chr4:75023664-75023714	Hepatocyte	liver:	n/a
9	chr4:75023664-75023714	HEK293	kidney:	embryo
10	chr4:75023664-75023714	HMEC	breast:	n/a
11	chr4:75023664-75023714	HCF	heart:	n/a
12	chr4:75023664-75023714	HUVEC	blood vessel:	n/a
13	chr4:75023664-75023714	BE2_C	brain:	n/a
14	chr4:75023664-75023714	HepG2	liver:	n/a
15	chr4:75023664-75023714	AG10803	skin:	n/a
16	chr4:75023664-75023714	SK-N-SH	brain:	n/a
17	chr4:75023664-75023714	U87	brain:	n/a
18	chr4:75023664-75023714	GM12878	blood:	n/a
19	chr4:75023664-75023714	ProgFib	skin:	n/a
20	chr4:75023664-75023714	HAEpiC	amniotic membrane:	n/a
21	chr4:75023664-75023714	HRE	kidney:	n/a
22	chr4:75023664-75023714	HCT-116	colon:	n/a
23	chr4:75023664-75023714	AG09309	skin:	n/a
24	chr4:75023664-75023714	SK-N-MC	brain:	n/a
25	chr4:75023664-75023714	A549	lung:	n/a
26	chr4:75023664-75023714	SK-N-SH_RA	brain:	n/a
27	chr4:75023664-75023714	SAEC	small airway:	n/a
28	chr4:75023664-75023714	GM12891	blood:	n/a
29	chr4:75023664-75023714	HCPEpiC	choroid plexus:	n/a
30	chr4:75023664-75023714	BJ	skin:	n/a
31	chr4:75023664-75023714	AG09319	gingival:	n/a
32	chr4:75023664-75023714	HL-60	blood:	n/a
33	chr4:75023664-75023714	Caco-2	colon:	n/a
34	chr4:75023664-75023714	PANC-1	pancreas:	n/a
35	chr4:75023664-75023714	HNPCEpiC	eye:	n/a
36	chr4:75023664-75023714	HPAEpiC	pulmonary alveolar:	n/a
37	chr4:75023664-75023714	NH-A	brain:	n/a
38	chr4:75023664-75023714	SKMC	muscle:	n/a
39	chr4:75023664-75023714	LNCaP	prostate:	n/a
40	chr4:75023664-75023714	PrEC	prostate:	n/a
41	chr4:75023664-75023714	GM12892	blood:	n/a
42	chr4:75023664-75023714	NB4	blood:	n/a
43	chr4:75023664-75023714	NT2-D1	testis:	n/a
44	chr4:75023664-75023714	GM19239	blood:	n/a
45	chr4:75023664-75023714	HRPEpiC	eye:	n/a
46	chr4:75023664-75023714	AG04449	skin:	fetal
47	chr4:75023664-75023714	RPTEC	kidney:	n/a
48	chr4:75023664-75023714	PFSK-1	brain:	n/a
49	chr4:75023664-75023714	MCF-7	breast:	n/a
50	chr4:75023664-75023714	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:74964506..74967065-chr4:75022087..75025561,3	K562	blood:
2	chr4:75023679..75024199-chr6:117923622..117924531,2	NB4	blood:
3	chr4:74122515..74124717-chr4:75023066..75024638,2	K562	blood:
4	chr4:75023332..75025369-chr4:75145514..75147366,2	MCF-7	breast:
5	chr4:75022872..75025434-chr4:75174456..75176612,2	MCF-7	breast:
6	chr4:75022222..75023752-chr4:75142957..75145413,2	K562	blood:
7	chr1:45196394..45197102-chr4:75023670..75024212,2	Hela-S3	cervix:
8	chr4:74920487..74923421-chr4:75023614..75026198,3	K562	blood:
9	chr20:277413..278096-chr4:75023404..75023960,2	NB4	blood:
10	chr4:75023013..75023782-chr6:27100367..27100877,2	Hela-S3	cervix:
11	chr4:75023432..75024127-chr7:115891562..115892062,2	NB4	blood:
12	chr4:74964506..74968474-chr4:75022087..75025768,6	K562	blood:

Variant related genes	Relation type
MTHFD2L	TF binding region
MTHFD2L	CpG island
ENSG00000196787	Chromatin interaction
ENSG00000135269	Chromatin interaction
ENSG00000200169	Chromatin interaction
ENSG00000177764	Chromatin interaction
ENSG00000081041	Chromatin interaction
ENSG00000132466	Chromatin interaction
ENSG00000248848	Chromatin interaction
ENSG00000163738	Chromatin interaction
ENSG00000047932	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000182585	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10008940	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10026869	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs10938111	0.82[EUR][1000 genomes]
rs12163831	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs12646785	1.00[CEU][hapmap];0.84[CHB][hapmap];0.92[GIH][hapmap];0.82[TSI][hapmap];0.89[EUR][1000 genomes]
rs1265346	0.81[EUR][1000 genomes]
rs13116686	0.89[EUR][1000 genomes]
rs13136363	1.00[CEU][hapmap];0.81[GIH][hapmap];1.00[EUR][1000 genomes]
rs1440404	0.89[JPT][hapmap];0.81[MEX][hapmap]
rs1440407	1.00[CEU][hapmap];0.83[CHB][hapmap];0.89[EUR][1000 genomes]
rs16850531	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs16850541	0.84[EUR][1000 genomes]
rs28823933	0.89[EUR][1000 genomes]
rs4694183	1.00[CEU][hapmap];0.92[GIH][hapmap];0.82[TSI][hapmap];0.89[EUR][1000 genomes]
rs479409	1.00[CEU][hapmap]
rs510884	1.00[CEU][hapmap];0.88[GIH][hapmap]
rs518475	1.00[CEU][hapmap];0.91[CHB][hapmap];0.84[EUR][1000 genomes]
rs519014	1.00[CEU][hapmap];0.86[CHB][hapmap];0.84[EUR][1000 genomes]
rs533352	1.00[CEU][hapmap];0.88[GIH][hapmap];0.84[EUR][1000 genomes]
rs537061	1.00[CEU][hapmap];0.84[CHB][hapmap];0.88[GIH][hapmap];0.84[EUR][1000 genomes]
rs538542	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs538775	1.00[CEU][hapmap];0.92[CHB][hapmap];0.84[CHD][hapmap];0.92[GIH][hapmap];0.88[MEX][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs542458	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs547975	1.00[CEU][hapmap];0.84[CHB][hapmap];0.84[EUR][1000 genomes]
rs551906	1.00[CEU][hapmap];0.84[CHB][hapmap];0.92[GIH][hapmap];0.84[EUR][1000 genomes]
rs564793	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs6446975	0.84[CHB][hapmap];0.82[TSI][hapmap];0.87[EUR][1000 genomes]
rs6446976	1.00[CEU][hapmap];0.84[CHB][hapmap];0.92[GIH][hapmap];0.82[TSI][hapmap];0.89[EUR][1000 genomes]
rs6824352	1.00[CEU][hapmap];0.88[GIH][hapmap];0.91[TSI][hapmap];0.95[EUR][1000 genomes]
rs977597	0.89[EUR][1000 genomes]
rs977598	1.00[CEU][hapmap];0.84[CHB][hapmap];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525980	chr4:74731526-75382209	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1004768	chr4:74774372-75109579	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv1006218	chr4:74782324-75105424	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv594683	chr4:75013441-75106485	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv1013260	chr4:75013441-75121643	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv1002907	chr4:75013441-75131443	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv1004706	chr4:75014770-75121643	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv594684	chr4:75015750-75106485	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	esv3346537	chr4:75022913-75025461	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 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	chr4:75022600-75025000	Active TSS	K562	blood
2	chr4:75022800-75023800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
3	chr4:75022800-75023800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr4:75022800-75024600	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr4:75022800-75025200	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr4:75022800-75025200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:75022800-75025400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr4:75023000-75023800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr4:75023000-75024400	Active TSS	Fetal Brain Female	brain
10	chr4:75023000-75024600	Active TSS	Stomach Mucosa	stomach
11	chr4:75023000-75024800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr4:75023000-75024800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr4:75023000-75024800	Active TSS	Colonic Mucosa	Colon
14	chr4:75023000-75025000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
15	chr4:75023000-75025000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
16	chr4:75023000-75025000	Active TSS	Fetal Muscle Trunk	muscle
17	chr4:75023000-75025000	Active TSS	Fetal Stomach	stomach
18	chr4:75023000-75025000	Active TSS	HepG2	liver
19	chr4:75023000-75025200	Active TSS	H1 Cell Line	embryonic stem cell
20	chr4:75023000-75025200	Active TSS	Thymus	Thymus
21	chr4:75023000-75025800	Active TSS	A549	lung
22	chr4:75023200-75023800	Flanking Active TSS	Primary B cells from cord blood	blood
23	chr4:75023200-75023800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
24	chr4:75023200-75024400	Active TSS	Fetal Brain Male	brain
25	chr4:75023200-75024400	Active TSS	Placenta Amnion	Placenta Amnion
26	chr4:75023200-75024600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr4:75023200-75024600	Active TSS	HUES64 Cell Line	embryonic stem cell
28	chr4:75023200-75024600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr4:75023200-75024600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr4:75023200-75024600	Active TSS	Brain Anterior Caudate	brain
31	chr4:75023200-75024600	Active TSS	Rectal Smooth Muscle	rectum
32	chr4:75023200-75024800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr4:75023200-75024800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
34	chr4:75023200-75024800	Active TSS	Left Ventricle	heart
35	chr4:75023200-75024800	Active TSS	Ovary	ovary
36	chr4:75023200-75024800	Active TSS	Pancreas	Pancrea
37	chr4:75023200-75025000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr4:75023200-75025000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr4:75023200-75025000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr4:75023200-75025200	Active TSS	Aorta	Aorta
41	chr4:75023200-75025200	Active TSS	Fetal Intestine Large	intestine
42	chr4:75023200-75025200	Active TSS	Fetal Intestine Small	intestine
43	chr4:75023200-75025400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr4:75023200-75025400	Active TSS	Psoas Muscle	Psoas
45	chr4:75023200-75025400	Active TSS	Right Ventricle	heart
46	chr4:75023400-75023800	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood
47	chr4:75023400-75024200	Active TSS	iPS-18 Cell Line	embryonic stem cell
48	chr4:75023400-75024200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
49	chr4:75023400-75024400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr4:75023400-75024400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links