Variant report

Variant	rs72718103
Chromosome Location	chr14:105287470-105287471
allele	C/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	MYC	chr14:105287393-105287472	HepG2	liver:	n/a	n/a
2	SMC3	chr14:105286812-105287570	SK-N-SH	brain:	n/a	chr14:105287195-105287205
3	POLR2A	chr14:105287082-105287962	Hela-S3	cervix:	n/a	n/a
4	MYBL2	chr14:105286934-105287501	HepG2	liver:	n/a	n/a
5	CTCF	chr14:105286709-105287706	SK-N-SH	brain:	n/a	n/a
6	MXI1	chr14:105286691-105287681	SK-N-SH	brain:	n/a	n/a
7	TCF7L2	chr14:105287134-105287527	PANC-1	pancreas:	n/a	chr14:105287477-105287493 chr14:105287477-105287493 chr14:105287478-105287492 chr14:105287481-105287490 chr14:105287479-105287489
8	MYBL2	chr14:105286971-105287766	HepG2	liver:	n/a	n/a
9	RAD21	chr14:105286947-105287505	MCF-7	breast:	n/a	chr14:105287287-105287300 chr14:105287243-105287257 chr14:105287219-105287233
10	CTCF	chr14:105287360-105287510	AG10803	skin:	n/a	n/a
11	HEY1	chr14:105286999-105287501	HepG2	liver:	n/a	n/a
12	MAX	chr14:105286969-105288097	HepG2	liver:	n/a	n/a
13	RAD21	chr14:105286932-105287482	H1-hESC	embryonic stem cell:	n/a	chr14:105287287-105287300 chr14:105287243-105287257 chr14:105287219-105287233
14	RAD21	chr14:105286945-105287526	MCF-7	breast:	n/a	chr14:105287287-105287300 chr14:105287243-105287257 chr14:105287219-105287233
15	CTCF	chr14:105287086-105287501	K562	blood:	n/a	n/a
16	MAX	chr14:105286871-105287478	A549	lung:	n/a	n/a
17	RAD21	chr14:105286966-105287520	HCT-116	colon:	n/a	chr14:105287287-105287300 chr14:105287243-105287257 chr14:105287219-105287233
18	RAD21	chr14:105286807-105287585	SK-N-SH	brain:	n/a	chr14:105287287-105287300 chr14:105287536-105287550 chr14:105287243-105287257 chr14:105287219-105287233
19	RAD21	chr14:105286938-105287491	A549	lung:	n/a	chr14:105287287-105287300 chr14:105287243-105287257 chr14:105287219-105287233
20	POLR2A	chr14:105286834-105287806	SK-N-MC	brain:	n/a	n/a
21	HA-E2F1	chr14:105287010-105287527	MCF-7	breast:	n/a	n/a
22	EP300	chr14:105287015-105287516	T-47D	breast:	n/a	chr14:105287040-105287054 chr14:105287224-105287240 chr14:105287116-105287132
23	CTCF	chr14:105286979-105287494	A549	lung:	n/a	n/a
24	POLR2A	chr14:105283941-105288196	HepG2	liver:	n/a	n/a
25	CTCF	chr14:105286889-105287548	MCF-7	breast:	n/a	n/a
26	NFIC	chr14:105287154-105287728	HepG2	liver:	n/a	n/a
27	MAZ	chr14:105286857-105287919	IMR90	lung:	n/a	n/a
28	EP300	chr14:105286974-105287507	A549	lung:	n/a	chr14:105287040-105287054 chr14:105287224-105287240 chr14:105287116-105287132
29	MAX	chr14:105286881-105287526	MCF-7	breast:	n/a	n/a
30	RAD21	chr14:105286985-105287473	ECC-1	luminal epithelium:	n/a	chr14:105287287-105287300 chr14:105287243-105287257 chr14:105287219-105287233
31	EP300	chr14:105286759-105287591	SK-N-SH	brain:	n/a	chr14:105286958-105286968 chr14:105286949-105286959 chr14:105287040-105287054 chr14:105287224-105287240 chr14:105287116-105287132
32	EP300	chr14:105287010-105287507	T-47D	breast:	n/a	chr14:105287040-105287054 chr14:105287224-105287240 chr14:105287116-105287132

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105287427-105287477	HCF	heart:	n/a
2	chr14:105287427-105287477	ECC-1	luminal epithelium:	n/a
3	chr14:105287427-105287477	AG10803	skin:	n/a
4	chr14:105287427-105287477	Hela-S3	cervix:	n/a
5	chr14:105287427-105287477	K562	blood:	n/a
6	chr14:105287427-105287477	HCPEpiC	choroid plexus:	n/a
7	chr14:105287427-105287477	H1-hESC	embryonic stem cell:	embryo
8	chr14:105287427-105287477	GM12891	blood:	n/a
9	chr14:105287427-105287477	HepG2	liver:	n/a
10	chr14:105287427-105287477	HCT-116	colon:	n/a
11	chr14:105287427-105287477	NB4	blood:	n/a
12	chr14:105287427-105287477	U87	brain:	n/a
13	chr14:105287427-105287477	MCF-7	breast:	n/a
14	chr14:105287427-105287477	AG09319	gingival:	n/a
15	chr14:105287427-105287477	SKMC	muscle:	n/a
16	chr14:105287427-105287477	LNCaP	prostate:	n/a
17	chr14:105287427-105287477	Caco-2	colon:	n/a
18	chr14:105287427-105287477	HPAEpiC	pulmonary alveolar:	n/a
19	chr14:105287427-105287477	AG04449	skin:	fetal
20	chr14:105287427-105287477	HL-60	blood:	n/a
21	chr14:105287427-105287477	AG09309	skin:	n/a
22	chr14:105287427-105287477	PrEC	prostate:	n/a
23	chr14:105287427-105287477	SK-N-SH	brain:	n/a
24	chr14:105287427-105287477	BJ	skin:	n/a
25	chr14:105287427-105287477	CMK	blood:	n/a
26	chr14:105287427-105287477	ovcar-3	ovarian:	n/a
27	chr14:105287427-105287477	SK-N-MC	brain:	n/a
28	chr14:105287427-105287477	MCF10A-Er-Src	breast:	n/a
29	chr14:105287427-105287477	BE2_C	brain:	n/a
30	chr14:105287427-105287477	AG04450	lung:	fetal
31	chr14:105287427-105287477	GM06990	blood:	n/a
32	chr14:105287427-105287477	Hepatocyte	liver:	n/a
33	chr14:105287427-105287477	SAEC	small airway:	n/a
34	chr14:105287427-105287477	PFSK-1	brain:	n/a
35	chr14:105287427-105287477	HUVEC	blood vessel:	n/a
36	chr14:105287427-105287477	IMR90	lung:	fetal
37	chr14:105287427-105287477	Jurkat	blood:	n/a
38	chr14:105287427-105287477	ProgFib	skin:	n/a
39	chr14:105287427-105287477	AoSMC	blood vessel:	n/a
40	chr14:105287427-105287477	A549	lung:	n/a
41	chr14:105287427-105287477	HIPEpiC	eye:	n/a
42	chr14:105287427-105287477	NHBE	bronchial:	n/a
43	chr14:105287427-105287477	HMEC	breast:	n/a
44	chr14:105287427-105287477	HRCEpiC	kidney:	n/a
45	chr14:105287427-105287477	SK-N-SH_RA	brain:	n/a
46	chr14:105287427-105287477	NT2-D1	testis:	n/a
47	chr14:105287427-105287477	GM12892	blood:	n/a
48	chr14:105287427-105287477	HEK293	kidney:	embryo
49	chr14:105287427-105287477	HAEpiC	amniotic membrane:	n/a
50	chr14:105287427-105287477	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:105190451..105191132-chr14:105286694..105287658,2	MCF-7	breast:
2	chr14:105217398..105221846-chr14:105284355..105288810,4	MCF-7	breast:
3	chr14:105284603..105287527-chr14:105343615..105347092,3	MCF-7	breast:
4	chr14:105259095..105269353-chr14:105280422..105289302,26	K562	blood:
5	chr14:105287373..105290281-chr14:105329548..105332218,5	MCF-7	breast:
6	chr14:105234579..105236355-chr14:105286684..105287712,12	MCF-7	breast:
7	chr14:105266435..105267408-chr14:105286766..105287693,2	MCF-7	breast:
8	chr14:105234538..105236569-chr14:105286438..105288492,2	K562	blood:
9	chr14:105286488..105288795-chr17:79479840..79482559,2	MCF-7	breast:
10	chr14:105285820..105287586-chr14:105330282..105332678,2	MCF-7	breast:
11	chr14:105189864..105192391-chr14:105285849..105287579,2	MCF-7	breast:

Variant related genes	Relation type
LINC00638	TF binding region
LINC00638	CpG island
ENSG00000179627	Chromatin interaction
ENSG00000229947	Chromatin interaction
ENSG00000184990	Chromatin interaction
ENSG00000184009	Chromatin interaction
ENSG00000142208	Chromatin interaction
ENSG00000099814	Chromatin interaction
ENSG00000185100	Chromatin interaction
ENSG00000229848	Chromatin interaction
ENSG00000258430	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10141861	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12050087	1.00[AFR][1000 genomes]
rs2841279	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34004095	1.00[AFR][1000 genomes]
rs3742938	1.00[AFR][1000 genomes]
rs41314519	1.00[AFR][1000 genomes]
rs57147900	1.00[AFR][1000 genomes]
rs57804458	1.00[AFR][1000 genomes]
rs58153756	1.00[AFR][1000 genomes]
rs58365272	1.00[AFR][1000 genomes]
rs61316883	1.00[AFR][1000 genomes]
rs61745186	1.00[AFR][1000 genomes]
rs61761195	1.00[AFR][1000 genomes]
rs7144557	1.00[AFR][1000 genomes]
rs72700126	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72700128	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72700150	1.00[AFR][1000 genomes]
rs72700170	1.00[AFR][1000 genomes]
rs72700172	1.00[AFR][1000 genomes]
rs72700175	1.00[AFR][1000 genomes]
rs72700176	1.00[AFR][1000 genomes]
rs72700183	1.00[AFR][1000 genomes]
rs72700187	1.00[AFR][1000 genomes]
rs72700189	1.00[AFR][1000 genomes]
rs72700192	1.00[AFR][1000 genomes]
rs72700202	1.00[AFR][1000 genomes]
rs72716002	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72718104	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72718105	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8012919	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530812	chr14:104775571-105364883	Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv1053591	chr14:105024558-105475931	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
3	nsv542224	chr14:105024558-105475931	Bivalent Enhancer Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
4	esv2830002	chr14:105078251-105348552	Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
5	nsv902388	chr14:105092479-105311249	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
6	nsv902389	chr14:105092479-105366499	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
7	esv1828345	chr14:105100787-105803170	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
8	nsv470677	chr14:105126354-105348552	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
9	nsv542225	chr14:105133688-105803170	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
10	nsv517038	chr14:105146579-105311249	Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
11	nsv566057	chr14:105146579-105311249	Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
12	nsv566060	chr14:105148655-105311249	Flanking Active TSS Genic enhancers Enhancers Bivalent Enhancer Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
13	nsv902404	chr14:105148655-105311249	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
14	nsv902405	chr14:105148655-105340643	Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
15	nsv902409	chr14:105154105-105311249	Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
16	nsv566063	chr14:105154105-105312935	Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
17	nsv542227	chr14:105157572-105803170	Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
18	nsv902412	chr14:105238701-105361934	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
19	esv1836552	chr14:105246686-105348552	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases
20	nsv902413	chr14:105246686-105366499	Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
21	esv1833474	chr14:105268228-105332154	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
22	nsv566093	chr14:105274093-105321835	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
23	esv1840298	chr14:105274292-105366499	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
24	nsv902416	chr14:105277209-105366499	Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
25	esv1803813	chr14:105285159-105293358	Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
26	nsv511540	chr14:105285159-105314093	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
27	nsv456456	chr14:105285159-105412541	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
28	nsv566099	chr14:105285159-105412541	Bivalent Enhancer Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105283200-105292200	Weak transcription	Gastric	stomach
2	chr14:105283400-105292000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr14:105283400-105292000	Weak transcription	Right Atrium	heart
4	chr14:105283600-105287600	Weak transcription	Brain Angular Gyrus	brain
5	chr14:105283600-105288800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr14:105283600-105292000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr14:105283600-105292000	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr14:105283800-105292000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr14:105283800-105292200	Weak transcription	Brain Cingulate Gyrus	brain
10	chr14:105284000-105288000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr14:105284000-105288800	Weak transcription	Spleen	Spleen
12	chr14:105284000-105289400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr14:105284000-105292000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr14:105284200-105288200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr14:105284400-105292200	Weak transcription	K562	blood
16	chr14:105284600-105290800	Weak transcription	Fetal Kidney	kidney
17	chr14:105285000-105287600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr14:105285000-105292200	Weak transcription	Dnd41	blood
19	chr14:105285200-105288400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr14:105286200-105288800	Enhancers	Fetal Stomach	stomach
21	chr14:105286400-105287600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr14:105286600-105287800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr14:105286600-105287800	Enhancers	A549	lung
24	chr14:105286800-105287600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr14:105286800-105287600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr14:105286800-105287600	Enhancers	Adipose Nuclei	Adipose
27	chr14:105286800-105287600	Enhancers	Liver	Liver
28	chr14:105286800-105287600	Enhancers	Fetal Intestine Small	intestine
29	chr14:105286800-105287600	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr14:105286800-105287600	Enhancers	HMEC	breast
31	chr14:105286800-105287600	Enhancers	HUVEC	blood vessel
32	chr14:105286800-105287800	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr14:105286800-105288000	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr14:105287000-105287600	Enhancers	Fetal Muscle Leg	muscle
35	chr14:105287000-105287600	Enhancers	HSMM	muscle
36	chr14:105287000-105287600	Enhancers	NHEK	skin
37	chr14:105287000-105287600	Enhancers	NHLF	lung
38	chr14:105287000-105287800	Enhancers	H1 Cell Line	embryonic stem cell
39	chr14:105287000-105287800	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr14:105287000-105287800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr14:105287000-105287800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr14:105287000-105287800	Enhancers	Esophagus	oesophagus
43	chr14:105287000-105287800	Enhancers	Left Ventricle	heart
44	chr14:105287000-105287800	Enhancers	Ovary	ovary
45	chr14:105287000-105288000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr14:105287000-105288000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
47	chr14:105287000-105288400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr14:105287000-105288600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr14:105287000-105288600	Enhancers	Placenta	Placenta
50	chr14:105287200-105287600	Enhancers	HUES48 Cell Line	embryonic stem cell

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