Variant report

Variant	rs4974560
Chromosome Location	chr4:1402372-1402373
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	REST	chr4:1402286-1402414	K562	blood:	n/a	chr4:1402290-1402310 chr4:1402297-1402310
2	RAD21	chr4:1402240-1402568	HepG2	liver:	n/a	n/a
3	CTCF	chr4:1402174-1402650	K562	blood:	n/a	chr4:1402397-1402410
4	CTCF	chr4:1402180-1402410	SK-N-SH_RA	brain:	n/a	chr4:1402397-1402410
5	CTCF	chr4:1402297-1402465	A549	lung:	n/a	chr4:1402397-1402410
6	CTCF	chr4:1402280-1402430	BE2_C	brain:	n/a	chr4:1402397-1402410
7	RAD21	chr4:1402168-1402565	HepG2	liver:	n/a	n/a
8	SMC3	chr4:1402330-1402516	K562	blood:	n/a	n/a
9	RAD21	chr4:1402214-1402574	ECC-1	luminal epithelium:	n/a	n/a
10	CTCF	chr4:1402330-1402482	LNCaP	prostate:	n/a	chr4:1402397-1402410
11	CTCF	chr4:1402248-1402525	H1-hESC	embryonic stem cell:	n/a	chr4:1402397-1402410
12	CTCF	chr4:1402360-1402510	HRE	kidney:	n/a	chr4:1402397-1402410
13	CTCF	chr4:1402328-1402471	A549	lung:	n/a	chr4:1402397-1402410
14	SUZ12	chr4:1395488-1403017	NT2-D1	testis:	n/a	n/a
15	RAD21	chr4:1402119-1402643	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr4:1402360-1402510	HRPEpiC	eye:	n/a	chr4:1402397-1402410
17	CTCF	chr4:1402218-1402466	K562	blood:	n/a	chr4:1402397-1402410
18	CTCF	chr4:1402293-1402433	SK-N-SH_RA	brain:	n/a	chr4:1402397-1402410
19	SUZ12	chr4:1402060-1402496	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr4:1402340-1402490	GM12873	blood:	n/a	chr4:1402397-1402410
21	CTCF	chr4:1402240-1402390	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr4:1402253-1402475	K562	blood:	n/a	chr4:1402397-1402410
23	CTCF	chr4:1402179-1402584	H1-hESC	embryonic stem cell:	n/a	chr4:1402397-1402410
24	CTCF	chr4:1402320-1402470	BE2_C	brain:	n/a	chr4:1402397-1402410
25	CTCF	chr4:1402300-1402450	HEK293	kidney:	n/a	chr4:1402397-1402410
26	REST	chr4:1402332-1402472	HepG2	liver:	n/a	chr4:1402457-1402470
27	CTCF	chr4:1402240-1402390	GM12874	blood:	n/a	n/a
28	RAD21	chr4:1402221-1402516	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr4:1402304-1402517	HepG2	liver:	n/a	chr4:1402397-1402410
30	RAD21	chr4:1402121-1402647	SK-N-SH	brain:	n/a	n/a
31	CTCF	chr4:1402320-1402470	HepG2	liver:	n/a	chr4:1402397-1402410
32	CTCF	chr4:1402320-1402487	Medullo	brain:	n/a	chr4:1402397-1402410
33	RAD21	chr4:1402341-1402462	K562	blood:	n/a	n/a
34	CTCF	chr4:1402340-1402490	WERI-Rb-1	eye:	n/a	chr4:1402397-1402410
35	CTCF	chr4:1402281-1402482	H1-hESC	embryonic stem cell:	n/a	chr4:1402397-1402410
36	CTCF	chr4:1402360-1402510	HEK293	kidney:	n/a	chr4:1402397-1402410
37	RAD21	chr4:1402314-1402488	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr4:1402333-1402437	SK-N-SH_RA	brain:	n/a	chr4:1402397-1402410
39	CTCF	chr4:1402280-1402430	HCFaa	heart:	n/a	chr4:1402397-1402410
40	RAD21	chr4:1402279-1402456	K562	blood:	n/a	n/a
41	CTCF	chr4:1402300-1402450	HMEC	breast:	n/a	chr4:1402397-1402410
42	CTCF	chr4:1402303-1402540	K562	blood:	n/a	chr4:1402397-1402410
43	CTCF	chr4:1402300-1402450	HRPEpiC	eye:	n/a	chr4:1402397-1402410
44	CTCF	chr4:1402260-1402410	HRE	kidney:	n/a	chr4:1402397-1402410
45	RAD21	chr4:1402228-1402546	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr4:1402320-1402478	K562	blood:	n/a	chr4:1402397-1402410
47	RAD21	chr4:1402264-1402554	HepG2	liver:	n/a	n/a
48	CTCF	chr4:1402288-1402485	HepG2	liver:	n/a	chr4:1402397-1402410
49	CTCF	chr4:1402294-1402485	LNCaP	prostate:	n/a	chr4:1402397-1402410
50	CTCF	chr4:1402320-1402470	K562	blood:	n/a	chr4:1402397-1402410

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1402343-1402393	BE2_C	brain:	n/a
2	chr4:1402343-1402393	HAEpiC	amniotic membrane:	n/a
3	chr4:1402343-1402393	IMR90	lung:	fetal
4	chr4:1402343-1402393	HUVEC	blood vessel:	n/a
5	chr4:1402343-1402393	AG09309	skin:	n/a
6	chr4:1402343-1402393	HCT-116	colon:	n/a
7	chr4:1402343-1402393	NH-A	brain:	n/a
8	chr4:1402343-1402393	MCF-7	breast:	n/a
9	chr4:1402343-1402393	HEEpiC	esophagus:	n/a
10	chr4:1402343-1402393	SK-N-MC	brain:	n/a
11	chr4:1402343-1402393	HRCEpiC	kidney:	n/a
12	chr4:1402343-1402393	CMK	blood:	n/a
13	chr4:1402343-1402393	PFSK-1	brain:	n/a
14	chr4:1402343-1402393	HIPEpiC	eye:	n/a
15	chr4:1402343-1402393	GM06990	blood:	n/a
16	chr4:1402343-1402393	SKMC	muscle:	n/a
17	chr4:1402343-1402393	GM12891	blood:	n/a
18	chr4:1402343-1402393	A549	lung:	n/a
19	chr4:1402343-1402393	GM12878	blood:	n/a
20	chr4:1402343-1402393	HL-60	blood:	n/a
21	chr4:1402343-1402393	K562	blood:	n/a
22	chr4:1402343-1402393	SAEC	small airway:	n/a
23	chr4:1402343-1402393	RPTEC	kidney:	n/a
24	chr4:1402343-1402393	HCF	heart:	n/a
25	chr4:1402343-1402393	PrEC	prostate:	n/a
26	chr4:1402343-1402393	ProgFib	skin:	n/a
27	chr4:1402343-1402393	HMEC	breast:	n/a
28	chr4:1402343-1402393	HepG2	liver:	n/a
29	chr4:1402343-1402393	AG10803	skin:	n/a
30	chr4:1402343-1402393	HCPEpiC	choroid plexus:	n/a
31	chr4:1402343-1402393	Hela-S3	cervix:	n/a
32	chr4:1402343-1402393	GM12892	blood:	n/a
33	chr4:1402343-1402393	T-47D	breast:	n/a
34	chr4:1402343-1402393	NHDF-neo	bronchial:	n/a
35	chr4:1402343-1402393	HPAEpiC	pulmonary alveolar:	n/a
36	chr4:1402343-1402393	AG04449	skin:	fetal
37	chr4:1402343-1402393	Jurkat	blood:	n/a
38	chr4:1402343-1402393	GM19239	blood:	n/a
39	chr4:1402343-1402393	AG09319	gingival:	n/a
40	chr4:1402343-1402393	NT2-D1	testis:	n/a
41	chr4:1402343-1402393	LNCaP	prostate:	n/a
42	chr4:1402343-1402393	AoSMC	blood vessel:	n/a
43	chr4:1402343-1402393	U87	brain:	n/a
44	chr4:1402343-1402393	HNPCEpiC	eye:	n/a
45	chr4:1402343-1402393	NB4	blood:	n/a
46	chr4:1402343-1402393	HRE	kidney:	n/a
47	chr4:1402343-1402393	Hepatocyte	liver:	n/a
48	chr4:1402343-1402393	HRPEpiC	eye:	n/a
49	chr4:1402343-1402393	BJ	skin:	n/a
50	chr4:1402343-1402393	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:1397408..1399062-chr4:1402095..1403760,2	K562	blood:
2	chr4:1391809..1396481-chr4:1400263..1404304,5	K562	blood:
3	chr4:1400709..1403410-chr4:1544391..1546329,2	K562	blood:
4	chr4:1398123..1401195-chr4:1402046..1405937,3	K562	blood:

Variant related genes	Relation type
NKX1-1	TF binding region
NKX1-1	CpG island
ENSG00000235608	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11248000	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11248001	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11248003	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11945310	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13116994	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13140229	0.81[ASN][1000 genomes]
rs4074691	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4246687	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4974620	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72613115	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7655221	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7665724	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7666322	0.97[ASN][1000 genomes]
rs7669940	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7684445	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7686106	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv822425	chr4:540105-1413799	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
2	esv3339080	chr4:970630-1546223	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
3	nsv878328	chr4:1141573-1990425	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
4	nsv878330	chr4:1147407-1523930	Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
5	nsv461152	chr4:1159680-1415698	Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
6	nsv593278	chr4:1159680-1415698	Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
7	nsv997971	chr4:1191256-1518521	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
8	nsv1002635	chr4:1282603-1402761	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
9	nsv878344	chr4:1291337-1414684	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
10	nsv878345	chr4:1291337-1563920	Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
11	nsv878347	chr4:1300077-1866358	Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
12	esv1794294	chr4:1307119-1817474	Bivalent/Poised TSS Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
13	nsv878350	chr4:1320023-1500753	Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Genic enhancers Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
14	nsv878351	chr4:1329847-1414684	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
15	nsv1008785	chr4:1335089-1518521	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
16	nsv536988	chr4:1335089-1518521	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
17	nsv593302	chr4:1338618-1414684	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
18	nsv870062	chr4:1376068-1523451	Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
19	nsv1003107	chr4:1380178-1710751	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
20	nsv1005964	chr4:1380178-1949459	Strong transcription Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
21	nsv870084	chr4:1389629-1563818	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
22	esv1821063	chr4:1391152-1420822	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
23	esv1829127	chr4:1391152-1496353	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
24	nsv878353	chr4:1392171-1549473	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
25	esv1799146	chr4:1392425-1423046	Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
26	nsv822436	chr4:1396452-1402757	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
27	esv3371034	chr4:1398152-1402550	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs4974560	UVSSA	cis	Skin Sun Exposed Lower leg	GTEx
rs4974560	UVSSA	cis	Whole Blood	GTEx
rs4974560	UVSSA	cis	Thyroid	GTEx
rs4974560	UVSSA	cis	Stomach	GTEx
rs4974560	CTBP1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1396800-1402600	Bivalent Enhancer	Fetal Brain Male	brain
2	chr4:1397600-1402400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:1398600-1402600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr4:1398800-1402400	Bivalent Enhancer	Right Ventricle	heart
5	chr4:1399800-1411200	Weak transcription	Right Atrium	heart
6	chr4:1400400-1403000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
7	chr4:1401400-1402400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr4:1402200-1402400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
9	chr4:1402200-1402400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:1402200-1402400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr4:1402200-1402400	Bivalent Enhancer	Esophagus	oesophagus
12	chr4:1402200-1402400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
13	chr4:1402200-1402400	Bivalent Enhancer	Fetal Brain Female	brain
14	chr4:1402200-1402400	Bivalent Enhancer	Lung	lung
15	chr4:1402200-1402600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr4:1402200-1402600	ZNF genes & repeats	Spleen	Spleen

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