Variant report

Variant	rs1967419
Chromosome Location	chr5:178017695-178017696
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	ZMIZ1	chr5:178017597-178018014	K562	blood:	n/a	n/a
2	CTCF	chr5:178017530-178017989	H1-hESC	embryonic stem cell:	n/a	n/a
3	RAD21	chr5:178017612-178018019	SK-N-SH_RA	brain:	n/a	n/a
4	CTCF	chr5:178017687-178017871	A549	lung:	n/a	n/a
5	RAD21	chr5:178017560-178018064	A549	lung:	n/a	n/a
6	RAD21	chr5:178017672-178017963	A549	lung:	n/a	n/a
7	HMGN3	chr5:178016799-178017736	K562	blood:	n/a	n/a
8	CCNT2	chr5:178016854-178017709	K562	blood:	n/a	n/a
9	CTCF	chr5:178017441-178018204	A549	lung:	n/a	n/a
10	POLR2A	chr5:178017330-178017723	GM12878	blood:	n/a	n/a
11	CTCF	chr5:178017621-178018170	IMR90	lung:	n/a	n/a
12	MAZ	chr5:178016820-178017893	IMR90	lung:	n/a	chr5:178016884-178016893
13	JUND	chr5:178017695-178017975	K562	blood:	n/a	n/a
14	MAX	chr5:178016795-178017730	ECC-1	luminal epithelium:	n/a	chr5:178016884-178016893
15	CTCF	chr5:178017623-178018073	MCF-7	breast:	n/a	n/a
16	SMC3	chr5:178017660-178018058	GM12878	blood:	n/a	n/a
17	CTCF	chr5:178017680-178017830	HMEC	breast:	n/a	n/a
18	RAD21	chr5:178017612-178017950	A549	lung:	n/a	n/a
19	CTCF	chr5:178017678-178017997	K562	blood:	n/a	n/a
20	MYC	chr5:178017590-178017985	K562	blood:	n/a	n/a
21	CTCF	chr5:178017677-178017989	NHEK	skin:	n/a	n/a
22	CTCF	chr5:178017685-178017974	LNCaP	prostate:	n/a	n/a
23	RAD21	chr5:178017490-178018075	SK-N-SH_RA	brain:	n/a	n/a
24	POLR2A	chr5:178015830-178017746	HL-60	blood:	n/a	n/a
25	RAD21	chr5:178017532-178018144	MCF-7	breast:	n/a	n/a
26	CTCF	chr5:178017678-178017914	A549	lung:	n/a	n/a
27	CTCF	chr5:178017680-178017830	HCM	heart:	n/a	n/a
28	EGR1	chr5:178017237-178017874	MCF-7	breast:	n/a	chr5:178017583-178017593 chr5:178017578-178017600 chr5:178017584-178017593 chr5:178017584-178017594 chr5:178017338-178017347 chr5:178017583-178017596 chr5:178017289-178017313 chr5:178017583-178017596 chr5:178017582-178017596 chr5:178017584-178017595 chr5:178017583-178017596 chr5:178017584-178017594 chr5:178017583-178017596 chr5:178017582-178017597
29	RAD21	chr5:178017683-178017864	GM12878	blood:	n/a	n/a
30	CTCF	chr5:178016464-178018361	SK-N-SH	brain:	n/a	n/a
31	EGR1	chr5:178017278-178017866	K562	blood:	n/a	chr5:178017583-178017593 chr5:178017578-178017600 chr5:178017584-178017593 chr5:178017584-178017594 chr5:178017338-178017347 chr5:178017583-178017596 chr5:178017289-178017313 chr5:178017583-178017596 chr5:178017582-178017596 chr5:178017584-178017595 chr5:178017583-178017596 chr5:178017584-178017594 chr5:178017583-178017596 chr5:178017582-178017597
32	RAD21	chr5:178017636-178017995	K562	blood:	n/a	n/a
33	ZNF143	chr5:178017682-178017998	K562	blood:	n/a	n/a
34	RAD21	chr5:178017635-178017976	K562	blood:	n/a	n/a
35	CTCF	chr5:178017661-178017945	A549	lung:	n/a	n/a
36	RAD21	chr5:178017665-178017976	MCF-7	breast:	n/a	n/a
37	EGR1	chr5:178017207-178017813	K562	blood:	n/a	chr5:178017583-178017593 chr5:178017578-178017600 chr5:178017584-178017593 chr5:178017584-178017594 chr5:178017338-178017347 chr5:178017583-178017596 chr5:178017289-178017313 chr5:178017583-178017596 chr5:178017582-178017596 chr5:178017584-178017595 chr5:178017583-178017596 chr5:178017584-178017594 chr5:178017583-178017596 chr5:178017223-178017236 chr5:178017582-178017597 chr5:178017222-178017237
38	SIN3A	chr5:178015731-178018014	H1-hESC	embryonic stem cell:	n/a	n/a
39	SMC3	chr5:178016946-178018049	K562	blood:	n/a	n/a
40	ZBTB7A	chr5:178016965-178018090	ECC-1	luminal epithelium:	n/a	chr5:178017669-178017676 chr5:178017902-178017909
41	MYC	chr5:178015818-178018032	NB4	blood:	n/a	chr5:178016731-178016741 chr5:178016884-178016893
42	RAD21	chr5:178017614-178017951	K562	blood:	n/a	n/a
43	SRF	chr5:178017151-178017709	ECC-1	luminal epithelium:	n/a	chr5:178017412-178017430
44	MAZ	chr5:178016902-178017906	K562	blood:	n/a	n/a
45	CTCF	chr5:178017523-178018082	MCF-7	breast:	n/a	n/a
46	RAD21	chr5:178016822-178018107	H1-hESC	embryonic stem cell:	n/a	chr5:178016825-178016838
47	EGR1	chr5:178017315-178017774	ECC-1	luminal epithelium:	n/a	chr5:178017583-178017593 chr5:178017578-178017600 chr5:178017584-178017593 chr5:178017584-178017594 chr5:178017338-178017347 chr5:178017583-178017596 chr5:178017583-178017596 chr5:178017582-178017596 chr5:178017584-178017595 chr5:178017583-178017596 chr5:178017584-178017594 chr5:178017583-178017596 chr5:178017582-178017597
48	BHLHE40	chr5:178017646-178018069	K562	blood:	n/a	n/a
49	RAD21	chr5:178017671-178017973	GM12878	blood:	n/a	n/a
50	RAD21	chr5:178016478-178018407	SK-N-SH	brain:	n/a	chr5:178016825-178016838

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178017667-178017717	BJ	skin:	n/a
2	chr5:178017669-178017719	RPTEC	kidney:	n/a
3	chr5:178017667-178017717	HCM	heart:	n/a
4	chr5:178017667-178017717	AG04449	skin:	fetal
5	chr5:178017667-178017717	AoSMC	blood vessel:	n/a
6	chr5:178017669-178017719	H1-hESC	embryonic stem cell:	embryo
7	chr5:178017669-178017719	MCF10A-Er-Src	breast:	n/a
8	chr5:178017669-178017719	HL-60	blood:	n/a
9	chr5:178017667-178017717	H1-hESC	embryonic stem cell:	embryo
10	chr5:178017667-178017717	AG04450	lung:	fetal
11	chr5:178017669-178017719	HUVEC	blood vessel:	n/a
12	chr5:178017667-178017717	NT2-D1	testis:	n/a
13	chr5:178017669-178017719	HEK293	kidney:	embryo
14	chr5:178017667-178017717	HCT-116	colon:	n/a
15	chr5:178017669-178017719	HRE	kidney:	n/a
16	chr5:178017667-178017717	Hepatocyte	liver:	n/a
17	chr5:178017667-178017717	Hela-S3	cervix:	n/a
18	chr5:178017667-178017717	A549	lung:	n/a
19	chr5:178017667-178017717	SK-N-SH	brain:	n/a
20	chr5:178017669-178017719	NHBE	bronchial:	n/a
21	chr5:178017669-178017719	A549	lung:	n/a
22	chr5:178017669-178017719	HMEC	breast:	n/a
23	chr5:178017669-178017719	HCPEpiC	choroid plexus:	n/a
24	chr5:178017669-178017719	NHDF-neo	bronchial:	n/a
25	chr5:178017669-178017719	IMR90	lung:	fetal
26	chr5:178017667-178017717	GM12892	blood:	n/a
27	chr5:178017667-178017717	NHDF-neo	bronchial:	n/a
28	chr5:178017669-178017719	PANC-1	pancreas:	n/a
29	chr5:178017667-178017717	HepG2	liver:	n/a
30	chr5:178017669-178017719	HCM	heart:	n/a
31	chr5:178017669-178017719	SK-N-MC	brain:	n/a
32	chr5:178017669-178017719	AG04450	lung:	fetal
33	chr5:178017667-178017717	NH-A	brain:	n/a
34	chr5:178017669-178017719	GM19239	blood:	n/a
35	chr5:178017667-178017717	HUVEC	blood vessel:	n/a
36	chr5:178017669-178017719	BJ	skin:	n/a
37	chr5:178017667-178017717	MCF-7	breast:	n/a
38	chr5:178017669-178017719	HNPCEpiC	eye:	n/a
39	chr5:178017669-178017719	PrEC	prostate:	n/a
40	chr5:178017669-178017719	ProgFib	skin:	n/a
41	chr5:178017667-178017717	HNPCEpiC	eye:	n/a
42	chr5:178017669-178017719	HCF	heart:	n/a
43	chr5:178017669-178017719	PFSK-1	brain:	n/a
44	chr5:178017669-178017719	GM06990	blood:	n/a
45	chr5:178017667-178017717	ECC-1	luminal epithelium:	n/a
46	chr5:178017667-178017717	PFSK-1	brain:	n/a
47	chr5:178017667-178017717	HIPEpiC	eye:	n/a
48	chr5:178017667-178017717	IMR90	lung:	fetal
49	chr5:178017667-178017717	SAEC	small airway:	n/a
50	chr5:178017667-178017717	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:177659189..177660088-chr5:178017540..178018315,2	K562	blood:
2	chr5:177631253..177632828-chr5:178016105..178018488,2	MCF-7	breast:

Variant related genes	Relation type
COL23A1	TF binding region
COL23A1	CpG island
ENSG00000175309	Chromatin interaction
ENSG00000197451	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10035557	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10051137	0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10061455	0.87[ASN][1000 genomes]
rs10061883	0.88[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs10064009	0.88[ASN][1000 genomes]
rs10065419	0.82[ASN][1000 genomes]
rs10070794	0.88[ASN][1000 genomes]
rs10073925	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10479501	0.88[ASN][1000 genomes]
rs11742564	0.92[ASN][1000 genomes]
rs11744815	0.92[ASN][1000 genomes]
rs11748909	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11953546	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs12654185	0.87[ASN][1000 genomes]
rs12654187	0.87[ASN][1000 genomes]
rs12719855	0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs13161074	0.83[ASN][1000 genomes]
rs13360296	0.88[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs1472457	0.88[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];0.93[YRI][hapmap];0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2335442	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs262021	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs262028	1.00[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs262036	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs388749	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4073633	0.88[ASN][1000 genomes]
rs4077796	0.94[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs4079109	0.88[ASN][1000 genomes]
rs4079111	0.88[ASN][1000 genomes]
rs4079112	0.86[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs4301240	0.88[ASN][1000 genomes]
rs4413550	0.88[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs4418123	0.88[ASN][1000 genomes]
rs4437394	0.88[ASN][1000 genomes]
rs4521498	0.92[ASN][1000 genomes]
rs4976798	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6600942	0.88[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs6866336	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6866952	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6869889	0.82[CEU][hapmap];0.88[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.89[ASN][1000 genomes]
rs6871074	0.91[ASN][1000 genomes]
rs6874126	0.82[ASN][1000 genomes]
rs6877022	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs721142	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs721143	0.94[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73353860	0.86[ASN][1000 genomes]
rs73353883	0.87[ASN][1000 genomes]
rs752043	0.85[CHB][hapmap];0.95[JPT][hapmap];0.91[YRI][hapmap];0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7707891	0.90[ASN][1000 genomes]
rs7715291	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7720708	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7736565	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs776153	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948342	chr5:177384542-178168737	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	141 gene(s)	inside rSNPs	diseases
2	nsv1029398	chr5:177502106-178070654	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	136 gene(s)	inside rSNPs	diseases
3	nsv883214	chr5:177876309-178047217	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1031666	chr5:177988601-178236068	Bivalent/Poised TSS Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv883216	chr5:178002325-178025087	Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	esv3431503	chr5:178015746-178018644	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178014600-178018000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
2	chr5:178015600-178017800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
3	chr5:178015800-178017800	Flanking Active TSS	Right Ventricle	heart
4	chr5:178016200-178017800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:178016200-178018000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
6	chr5:178016200-178018200	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
7	chr5:178016400-178017800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr5:178016400-178018000	Active TSS	H9 Cell Line	embryonic stem cell
9	chr5:178016400-178018000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
10	chr5:178016600-178017800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
11	chr5:178016600-178017800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
12	chr5:178016600-178017800	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr5:178016600-178017800	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr5:178016600-178017800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
15	chr5:178016600-178017800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr5:178016600-178017800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr5:178016600-178017800	Active TSS	Brain Substantia Nigra	brain
18	chr5:178016600-178017800	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
19	chr5:178016600-178017800	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
20	chr5:178016600-178017800	Bivalent/Poised TSS	NHDF-Ad	bronchial
21	chr5:178016600-178018000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
22	chr5:178016600-178018000	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr5:178016600-178018000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr5:178016600-178018000	Active TSS	Brain Angular Gyrus	brain
25	chr5:178016600-178018000	Bivalent Enhancer	Fetal Brain Male	brain
26	chr5:178016600-178018000	Active TSS	Rectal Smooth Muscle	rectum
27	chr5:178016600-178018200	Active TSS	Aorta	Aorta
28	chr5:178016600-178018400	Flanking Active TSS	Stomach Smooth Muscle	stomach
29	chr5:178016800-178017800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
30	chr5:178016800-178017800	Active TSS	iPS-15b Cell Line	embryonic stem cell
31	chr5:178016800-178017800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr5:178016800-178017800	Flanking Active TSS	Primary hematopoietic stem cells	blood
33	chr5:178016800-178017800	Flanking Active TSS	Esophagus	oesophagus
34	chr5:178016800-178017800	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
35	chr5:178016800-178017800	Flanking Bivalent TSS/Enh	Thymus	Thymus
36	chr5:178016800-178017800	Bivalent/Poised TSS	NH-A	brain
37	chr5:178016800-178018000	Active TSS	Primary T cells from cord blood	blood
38	chr5:178016800-178018000	Active TSS	Brain Inferior Temporal Lobe	brain
39	chr5:178016800-178018200	Active TSS	Breast Myoepithelial Primary Cells	Breast
40	chr5:178016800-178018400	Flanking Active TSS	HMEC	breast
41	chr5:178017000-178017800	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr5:178017000-178017800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr5:178017000-178017800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr5:178017000-178017800	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
45	chr5:178017000-178017800	Active TSS	Left Ventricle	heart
46	chr5:178017000-178017800	Active TSS	Ovary	ovary
47	chr5:178017000-178017800	Active TSS	Rectal Mucosa Donor 31	rectum
48	chr5:178017000-178017800	Active TSS	Right Atrium	heart
49	chr5:178017000-178017800	Active TSS	HSMMtube	muscle
50	chr5:178017000-178018000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links