Variant report

Variant	rs33984772
Chromosome Location	chr14:38060646-38060647
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:64)
CpG islands
(count:0)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:64 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RAD21	chr14:38060469-38061257	H1-hESC	embryonic stem cell:	n/a	n/a
2	MAX	chr14:38060607-38061760	H1-hESC	embryonic stem cell:	n/a	n/a
3	POLR2A	chr14:38060286-38060704	H1-neurons	neurons:	n/a	n/a
4	CTCF	chr14:38060292-38061770	A549	lung:	n/a	n/a
5	CTCF	chr14:38060500-38060650	HMF	breast:	n/a	n/a
6	ZNF143	chr14:38060537-38061196	H1-hESC	embryonic stem cell:	n/a	n/a
7	POLR2A	chr14:38060637-38060790	A549	lung:	n/a	n/a
8	POLR2A	chr14:38060633-38060874	MCF-7	breast:	n/a	n/a
9	POLR2A	chr14:38060558-38062366	MCF-7	breast:	n/a	n/a
10	CTCF	chr14:38060602-38061149	A549	lung:	n/a	n/a
11	CTCF	chr14:38060609-38061140	MCF-7	breast:	n/a	n/a
12	PML	chr14:38060516-38062586	MCF-7	breast:	n/a	n/a
13	TBP	chr14:38060611-38061129	H1-hESC	embryonic stem cell:	n/a	n/a
14	SIN3AK20	chr14:38060259-38066080	MCF-7	breast:	n/a	n/a
15	MAX	chr14:38060594-38061847	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr14:38060600-38060750	HRPEpiC	eye:	n/a	n/a
17	GATA3	chr14:38060472-38061020	T-47D	breast:	n/a	n/a
18	HDAC2	chr14:38060392-38062489	MCF-7	breast:	n/a	n/a
19	POLR2A	chr14:38059249-38060948	HepG2	liver:	n/a	n/a
20	CTCF	chr14:38060560-38060710	HRE	kidney:	n/a	n/a
21	FOXA1	chr14:38060408-38061116	T-47D	breast:	n/a	n/a
22	PML	chr14:38060460-38062367	MCF-7	breast:	n/a	n/a
23	CTCF	chr14:38060600-38060750	HEEpiC	esophagus:	n/a	n/a
24	MAX	chr14:38060450-38061961	A549	lung:	n/a	n/a
25	CTCF	chr14:38060620-38060770	MCF-7	breast:	n/a	n/a
26	POLR2A	chr14:38059317-38060922	HepG2	liver:	n/a	n/a
27	SUZ12	chr14:38060504-38060929	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr14:38060571-38061145	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr14:38060560-38060710	HBMEC	blood vessel:	n/a	n/a
30	POLR2A	chr14:38060432-38062293	ProgFib	skin:	n/a	n/a
31	YY1	chr14:38060591-38061145	H1-hESC	embryonic stem cell:	n/a	n/a
32	HEY1	chr14:38059398-38060907	HepG2	liver:	n/a	n/a
33	CHD1	chr14:38060477-38060869	H1-hESC	embryonic stem cell:	n/a	n/a
34	NR2F2	chr14:38060475-38062546	MCF-7	breast:	n/a	n/a
35	POLR2A	chr14:38059381-38060945	HepG2	liver:	n/a	n/a
36	FOXA2	chr14:38057014-38060700	HepG2	liver:	n/a	n/a
37	POLR2A	chr14:38060381-38060889	HepG2	liver:	n/a	n/a
38	EP300	chr14:38060525-38061219	T-47D	breast:	n/a	n/a
39	CTCF	chr14:38060399-38061396	MCF-7	breast:	n/a	n/a
40	CTCF	chr14:38060455-38061224	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTBP2	chr14:38060581-38062070	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr14:38060580-38060730	HCPEpiC	choroid plexus:	n/a	n/a
43	POLR2A	chr14:38059290-38065931	MCF-7	breast:	n/a	n/a
44	CTCF	chr14:38060600-38060750	Caco-2	colon:	n/a	n/a
45	RAD21	chr14:38060546-38061181	H1-hESC	embryonic stem cell:	n/a	n/a
46	MAX	chr14:38060376-38062437	MCF-7	breast:	n/a	n/a
47	MAX	chr14:38060540-38060891	H1-hESC	embryonic stem cell:	n/a	n/a
48	TCF12	chr14:38060504-38062183	A549	lung:	n/a	n/a
49	JUND	chr14:38060359-38062588	MCF-7	breast:	n/a	n/a
50	ELF1	chr14:38060497-38062465	MCF-7	breast:	n/a	chr14:38061946-38061958

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:37744550..37746871-chr14:38059550..38062065,2	MCF-7	breast:
2	chr14:38043804..38045954-chr14:38058287..38060752,2	K562	blood:
3	chr14:37996620..37999759-chr14:38060620..38062986,3	MCF-7	breast:
4	chr14:37924566..37927073-chr14:38060566..38062784,2	MCF-7	breast:
5	chr14:38003108..38005323-chr14:38059907..38061947,2	MCF-7	breast:
6	chr14:38060623..38062543-chr4:141076075..141078577,2	MCF-7	breast:
7	chr14:38055708..38063394-chr14:38063498..38068319,8	K562	blood:
8	chr14:37731472..37733246-chr14:38060600..38063260,2	MCF-7	breast:
9	chr14:38060569..38062165-chr14:38339643..38341361,2	MCF-7	breast:
10	chr14:38059647..38062011-chr19:58890686..58893348,2	MCF-7	breast:
11	chr14:38059772..38062294-chr6:35436080..35437583,2	MCF-7	breast:
12	chr14:37709149..37730989-chr14:38048141..38067789,135	MCF-7	breast:
13	chr14:38035708..38036563-chr14:38060466..38061108,2	MCF-7	breast:
14	chr14:38058730..38062004-chr14:38152244..38154718,3	MCF-7	breast:
15	chr14:38060438..38062133-chr14:38130712..38132708,2	MCF-7	breast:
16	chr14:38010426..38020494-chr14:38050537..38062032,33	MCF-7	breast:
17	chr14:37708906..37733371-chr14:38048131..38068843,170	MCF-7	breast:
18	chr14:38009151..38011590-chr14:38058939..38061053,2	MCF-7	breast:
19	chr14:37903287..37907312-chr14:38059908..38064571,5	MCF-7	breast:

No data

Variant related genes	Relation type
TTC6	TF binding region
ENSG00000152475	Chromatin interaction
ENSG00000198755	Chromatin interaction
ENSG00000207046	Chromatin interaction
ENSG00000139865	Chromatin interaction
ENSG00000259087	Chromatin interaction
ENSG00000151338	Chromatin interaction
ENSG00000129514	Chromatin interaction

Extended variants
information (count: 133 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:121)

rs_ID	r²[population]
rs12147674	1.00[AFR][1000 genomes]
rs12878124	1.00[AFR][1000 genomes]
rs12878633	1.00[AFR][1000 genomes]
rs12878710	1.00[AFR][1000 genomes]
rs12878846	1.00[AFR][1000 genomes]
rs12879149	1.00[AFR][1000 genomes]
rs12879319	1.00[AFR][1000 genomes]
rs12882123	1.00[AFR][1000 genomes]
rs12882687	1.00[AFR][1000 genomes]
rs12882773	1.00[AFR][1000 genomes]
rs12887471	1.00[AFR][1000 genomes]
rs12887758	1.00[AFR][1000 genomes]
rs12888451	1.00[AFR][1000 genomes]
rs12889687	1.00[AFR][1000 genomes]
rs12889859	1.00[AFR][1000 genomes]
rs12890074	1.00[AFR][1000 genomes]
rs12890845	1.00[AFR][1000 genomes]
rs12893402	1.00[AFR][1000 genomes]
rs12894394	1.00[AFR][1000 genomes]
rs12896790	1.00[AFR][1000 genomes]
rs12897309	1.00[AFR][1000 genomes]
rs17106861	0.93[EUR][1000 genomes]
rs17179274	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17179281	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17179609	1.00[AFR][1000 genomes]
rs17768440	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17768654	1.00[AFR][1000 genomes]
rs34025516	1.00[AFR][1000 genomes]
rs34043056	1.00[AFR][1000 genomes]
rs34069628	1.00[AFR][1000 genomes]
rs34184341	1.00[AFR][1000 genomes]
rs34242177	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34256053	1.00[AFR][1000 genomes]
rs34265999	1.00[AFR][1000 genomes]
rs34273412	1.00[AFR][1000 genomes]
rs34306117	1.00[AFR][1000 genomes]
rs34338696	1.00[AFR][1000 genomes]
rs34434018	1.00[AFR][1000 genomes]
rs34450997	1.00[AFR][1000 genomes]
rs34469876	1.00[AFR][1000 genomes]
rs34496783	1.00[AFR][1000 genomes]
rs34516219	1.00[AFR][1000 genomes]
rs34543736	1.00[AFR][1000 genomes]
rs34548330	1.00[AFR][1000 genomes]
rs34567961	1.00[AFR][1000 genomes]
rs34586390	1.00[AFR][1000 genomes]
rs34680819	1.00[AFR][1000 genomes]
rs34747911	1.00[AFR][1000 genomes]
rs34813864	1.00[AFR][1000 genomes]
rs34830744	1.00[AFR][1000 genomes]
rs34886614	1.00[AFR][1000 genomes]
rs35030337	1.00[AFR][1000 genomes]
rs35074434	1.00[AFR][1000 genomes]
rs35082276	1.00[AFR][1000 genomes]
rs35110244	1.00[AFR][1000 genomes]
rs35111962	1.00[AFR][1000 genomes]
rs35141852	1.00[AFR][1000 genomes]
rs35169093	1.00[AFR][1000 genomes]
rs35190835	1.00[AFR][1000 genomes]
rs35294705	1.00[AFR][1000 genomes]
rs35310265	1.00[AFR][1000 genomes]
rs35319231	1.00[AFR][1000 genomes]
rs35330350	1.00[AFR][1000 genomes]
rs35333548	1.00[AFR][1000 genomes]
rs35347282	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35350493	1.00[AFR][1000 genomes]
rs35383091	1.00[AFR][1000 genomes]
rs35393462	1.00[AFR][1000 genomes]
rs35413274	1.00[AFR][1000 genomes]
rs35427651	1.00[AFR][1000 genomes]
rs35435404	1.00[AFR][1000 genomes]
rs35438963	1.00[AFR][1000 genomes]
rs35441075	1.00[AFR][1000 genomes]
rs35470726	1.00[AFR][1000 genomes]
rs35505269	1.00[AFR][1000 genomes]
rs35536208	1.00[AFR][1000 genomes]
rs35610918	1.00[AFR][1000 genomes]
rs35699962	1.00[AFR][1000 genomes]
rs35706871	1.00[AFR][1000 genomes]
rs35748911	1.00[AFR][1000 genomes]
rs35791659	1.00[AFR][1000 genomes]
rs35802121	1.00[AFR][1000 genomes]
rs35852338	1.00[AFR][1000 genomes]
rs35891950	1.00[AFR][1000 genomes]
rs35926829	1.00[AFR][1000 genomes]
rs35926928	1.00[AFR][1000 genomes]
rs35942161	1.00[AFR][1000 genomes]
rs36004540	1.00[AFR][1000 genomes]
rs36044547	1.00[AFR][1000 genomes]
rs36074427	1.00[AFR][1000 genomes]
rs36189403	1.00[AFR][1000 genomes]
rs36194865	1.00[AFR][1000 genomes]
rs55734217	1.00[AFR][1000 genomes]
rs55972477	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56223359	1.00[AFR][1000 genomes]
rs71405800	1.00[AFR][1000 genomes]
rs71407707	1.00[AFR][1000 genomes]
rs71407708	1.00[AFR][1000 genomes]
rs71407709	1.00[AFR][1000 genomes]
rs71407710	1.00[AFR][1000 genomes]
rs71407711	1.00[AFR][1000 genomes]
rs71407712	1.00[AFR][1000 genomes]
rs71407716	1.00[AFR][1000 genomes]
rs71407717	1.00[AFR][1000 genomes]
rs71407718	1.00[AFR][1000 genomes]
rs71407720	1.00[AFR][1000 genomes]
rs71407721	1.00[AFR][1000 genomes]
rs71407722	1.00[AFR][1000 genomes]
rs71407723	1.00[AFR][1000 genomes]
rs71407724	1.00[AFR][1000 genomes]
rs71407725	1.00[AFR][1000 genomes]
rs71407726	1.00[AFR][1000 genomes]
rs71407727	1.00[AFR][1000 genomes]
rs71407728	1.00[AFR][1000 genomes]
rs71407729	1.00[AFR][1000 genomes]
rs71407730	1.00[AFR][1000 genomes]
rs71407731	1.00[AFR][1000 genomes]
rs71407732	1.00[AFR][1000 genomes]
rs71407733	1.00[AFR][1000 genomes]
rs71407734	1.00[AFR][1000 genomes]
rs71407741	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530038	chr14:37590543-38336191	Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv826923	chr14:38017619-38108645	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
3	nsv832772	chr14:38030300-38225921	Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
4	nsv901642	chr14:38041870-38081005	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
5	nsv901643	chr14:38047789-38081005	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
6	nsv901644	chr14:38049107-38064738	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
7	nsv901645	chr14:38051035-38064215	Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
8	nsv901646	chr14:38051035-38081005	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
9	nsv901647	chr14:38052110-38064738	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
10	nsv901648	chr14:38052110-38065813	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
11	nsv916985	chr14:38052347-38838551	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases
12	nsv901649	chr14:38053334-38065813	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38053400-38062800	Weak transcription	Hela-S3	cervix
2	chr14:38056200-38065600	Bivalent/Poised TSS	Fetal Intestine Small	intestine
3	chr14:38056400-38066000	Bivalent/Poised TSS	Fetal Intestine Large	intestine
4	chr14:38057000-38065400	Active TSS	Liver	Liver
5	chr14:38057800-38060800	Weak transcription	Pancreas	Pancrea
6	chr14:38058600-38062200	Active TSS	Rectal Mucosa Donor 29	rectum
7	chr14:38059400-38061000	Transcr. at gene 5' and 3'	HepG2	liver
8	chr14:38059600-38060800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr14:38059600-38063200	Bivalent/Poised TSS	Stomach Mucosa	stomach
10	chr14:38059800-38065600	Active TSS	A549	lung
11	chr14:38060000-38063200	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
12	chr14:38060200-38062400	Bivalent/Poised TSS	Colonic Mucosa	Colon
13	chr14:38060400-38060800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr14:38060400-38060800	Bivalent/Poised TSS	Primary T cells from cord blood	blood
15	chr14:38060400-38060800	Bivalent/Poised TSS	Fetal Lung	lung
16	chr14:38060400-38061000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
17	chr14:38060400-38061200	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
18	chr14:38060400-38061600	Bivalent/Poised TSS	Esophagus	oesophagus
19	chr14:38060400-38062200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
20	chr14:38060400-38062400	Bivalent/Poised TSS	Small Intestine	intestine
21	chr14:38060400-38064000	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
22	chr14:38060600-38060800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
23	chr14:38060600-38060800	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr14:38060600-38060800	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr14:38060600-38060800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
26	chr14:38060600-38060800	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
27	chr14:38060600-38060800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr14:38060600-38060800	Bivalent Enhancer	Brain Hippocampus Middle	brain
29	chr14:38060600-38060800	Bivalent Enhancer	Fetal Heart	heart
30	chr14:38060600-38060800	Bivalent Enhancer	Left Ventricle	heart
31	chr14:38060600-38060800	Bivalent Enhancer	Psoas Muscle	Psoas
32	chr14:38060600-38060800	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 31	rectum
33	chr14:38060600-38060800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
34	chr14:38060600-38061000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
35	chr14:38060600-38061000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr14:38060600-38061000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr14:38060600-38061000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr14:38060600-38061000	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
39	chr14:38060600-38061200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr14:38060600-38061400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr14:38060600-38061400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
42	chr14:38060600-38061400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
43	chr14:38060600-38061600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr14:38060600-38061600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
45	chr14:38060600-38061800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr14:38060600-38061800	Bivalent Enhancer	HMEC	breast
47	chr14:38060600-38062000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
48	chr14:38060600-38062000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
49	chr14:38060600-38062000	Bivalent Enhancer	Spleen	Spleen
50	chr14:38060600-38062200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell

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