Variant report

Variant	rs74089807
Chromosome Location	chr14:105557746-105557747
allele	C/T
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	MAX	chr14:105556409-105559034	MCF-7	breast:	n/a	chr14:105558119-105558129 chr14:105558711-105558721 chr14:105558880-105558895 chr14:105558887-105558897
2	BCL3	chr14:105557664-105559598	A549	lung:	n/a	chr14:105558706-105558719 chr14:105559120-105559133
3	TCF12	chr14:105556669-105559848	ECC-1	luminal epithelium:	n/a	chr14:105558705-105558715 chr14:105556711-105556721 chr14:105558506-105558516 chr14:105558328-105558335 chr14:105556879-105556889 chr14:105556900-105556910 chr14:105558295-105558305 chr14:105557507-105557514
4	MYC	chr14:105556712-105559367	A549	lung:	n/a	chr14:105558119-105558129 chr14:105558711-105558721 chr14:105558880-105558895 chr14:105559297-105559307 chr14:105558887-105558897
5	ESR1	chr14:105557737-105558500	ECC-1	luminal epithelium:	n/a	n/a
6	POLR2A	chr14:105557226-105561146	A549	lung:	n/a	n/a
7	BCL3	chr14:105556352-105559650	A549	lung:	n/a	chr14:105559601-105559614 chr14:105558706-105558719 chr14:105559120-105559133
8	FOXM1	chr14:105556756-105558866	ECC-1	luminal epithelium:	n/a	n/a
9	FOXM1	chr14:105557620-105558401	MCF-7	breast:	n/a	n/a
10	RAD21	chr14:105557668-105558707	ECC-1	luminal epithelium:	n/a	chr14:105558217-105558227 chr14:105558452-105558464 chr14:105558088-105558098 chr14:105558320-105558333
11	MAX	chr14:105556809-105559855	ECC-1	luminal epithelium:	n/a	chr14:105558119-105558129 chr14:105558711-105558721 chr14:105558880-105558895 chr14:105559297-105559307 chr14:105559437-105559447 chr14:105558887-105558897
12	TCF12	chr14:105552661-105561002	A549	lung:	n/a	chr14:105555506-105555515 chr14:105554733-105554741 chr14:105554099-105554109 chr14:105560562-105560572 chr14:105558705-105558715 chr14:105556711-105556721 chr14:105560974-105560982 chr14:105558506-105558516 chr14:105555994-105556004 chr14:105558328-105558335 chr14:105556609-105556616 chr14:105556879-105556889 chr14:105556900-105556910 chr14:105558295-105558305 chr14:105557507-105557514
13	EP300	chr14:105557476-105558527	MCF-7	breast:	n/a	chr14:105557498-105557514 chr14:105558269-105558285
14	NR3C1	chr14:105557662-105559108	A549	lung:	n/a	chr14:105557679-105557692
15	TEAD4	chr14:105557715-105558718	A549	lung:	n/a	n/a
16	SIN3AK20	chr14:105557504-105558485	MCF-7	breast:	n/a	n/a
17	TEAD4	chr14:105557686-105558483	HCT-116	colon:	n/a	n/a
18	SIX5	chr14:105557722-105558216	A549	lung:	n/a	n/a
19	GATA3	chr14:105557530-105558593	MCF-7	breast:	n/a	chr14:105558243-105558250
20	E2F6	chr14:105557679-105559822	A549	lung:	n/a	chr14:105559639-105559648 chr14:105559574-105559583 chr14:105559645-105559654 chr14:105559790-105559797 chr14:105559118-105559128
21	SRF	chr14:105557669-105558704	ECC-1	luminal epithelium:	n/a	n/a
22	TEAD4	chr14:105556774-105558874	ECC-1	luminal epithelium:	n/a	n/a
23	POLR2A	chr14:105557708-105560589	HCT-116	colon:	n/a	n/a
24	NR3C1	chr14:105557718-105558872	A549	lung:	n/a	n/a
25	POLR2A	chr14:105557554-105560595	A549	lung:	n/a	n/a
26	EP300	chr14:105557228-105558827	ECC-1	luminal epithelium:	n/a	chr14:105557498-105557514 chr14:105557385-105557401 chr14:105558269-105558285
27	CTCF	chr14:105556356-105557812	MCF-7	breast:	n/a	chr14:105556805-105556818 chr14:105556998-105557011 chr14:105556547-105556560 chr14:105556857-105556866 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105557447-105557455 chr14:105557501-105557514 chr14:105556998-105557011 chr14:105556998-105557007 chr14:105557444-105557462
28	HDAC2	chr14:105556473-105559201	MCF-7	breast:	n/a	chr14:105557047-105557056
29	ELF1	chr14:105557588-105558443	MCF-7	breast:	n/a	n/a
30	ELF1	chr14:105557636-105558732	MCF-7	breast:	n/a	n/a
31	MAX	chr14:105557586-105558405	MCF-7	breast:	n/a	chr14:105558119-105558129
32	EGR1	chr14:105557727-105558484	MCF-7	breast:	n/a	chr14:105558119-105558134 chr14:105558123-105558132 chr14:105558120-105558133
33	EP300	chr14:105556632-105561231	ECC-1	luminal epithelium:	n/a	chr14:105559405-105559421 chr14:105557498-105557514 chr14:105559121-105559137 chr14:105557385-105557401 chr14:105556882-105556898 chr14:105559636-105559652 chr14:105558269-105558285
34	TCF12	chr14:105556770-105559846	ECC-1	luminal epithelium:	n/a	chr14:105558705-105558715 chr14:105558506-105558516 chr14:105558328-105558335 chr14:105556879-105556889 chr14:105556900-105556910 chr14:105558295-105558305 chr14:105557507-105557514
35	ZBTB7A	chr14:105556759-105561147	ECC-1	luminal epithelium:	n/a	chr14:105559442-105559450 chr14:105557003-105557012
36	JUND	chr14:105557310-105559380	A549	lung:	n/a	chr14:105558659-105558673 chr14:105559299-105559308
37	SP1	chr14:105556409-105559717	A549	lung:	n/a	chr14:105558852-105558866 chr14:105556553-105556562 chr14:105559432-105559446 chr14:105559068-105559078 chr14:105558120-105558129 chr14:105558467-105558481 chr14:105558084-105558096 chr14:105556549-105556563 chr14:105557021-105557030 chr14:105559300-105559309 chr14:105557838-105557852 chr14:105558179-105558189 chr14:105558118-105558130 chr14:105559573-105559585 chr14:105558118-105558130 chr14:105556552-105556564 chr14:105559068-105559082 chr14:105558886-105558898 chr14:105559067-105559079 chr14:105558851-105558864 chr14:105558886-105558898 chr14:105559575-105559584 chr14:105559068-105559077 chr14:105558119-105558129 chr14:105559069-105559078 chr14:105558887-105558897 chr14:105558119-105558128 chr14:105558856-105558865 chr14:105559068-105559078
38	CEBPB	chr14:105557734-105558479	ECC-1	luminal epithelium:	n/a	n/a
39	GABPA	chr14:105557709-105558416	MCF-7	breast:	n/a	chr14:105558119-105558128
40	ZBTB33	chr14:105557654-105558509	A549	lung:	n/a	n/a
41	TCF7L2	chr14:105557320-105558682	Hela-S3	cervix:	n/a	chr14:105558144-105558160 chr14:105558144-105558160 chr14:105558148-105558158 chr14:105558147-105558156 chr14:105558145-105558159 chr14:105558145-105558159
42	POLR2A	chr14:105557654-105559803	HCT-116	colon:	n/a	n/a
43	EP300	chr14:105556277-105559811	A549	lung:	n/a	chr14:105559405-105559421 chr14:105557498-105557514 chr14:105559121-105559137 chr14:105557385-105557401 chr14:105556882-105556898 chr14:105559636-105559652 chr14:105558269-105558285
44	POLR2A	chr14:105557741-105560748	ECC-1	luminal epithelium:	n/a	n/a
45	ETS1	chr14:105557711-105559732	A549	lung:	n/a	chr14:105559572-105559583 chr14:105558854-105558865 chr14:105559297-105559308 chr14:105558263-105558276
46	GATA3	chr14:105556580-105558477	MCF-7	breast:	n/a	chr14:105558243-105558250
47	MAX	chr14:105557289-105560967	ECC-1	luminal epithelium:	n/a	chr14:105558119-105558129 chr14:105560838-105560848 chr14:105558711-105558721 chr14:105558880-105558895 chr14:105559297-105559307 chr14:105559437-105559447 chr14:105558887-105558897
48	NFIC	chr14:105557676-105558411	SK-N-SH	brain:	n/a	n/a
49	FOSL2	chr14:105557664-105559409	A549	lung:	n/a	chr14:105558659-105558673 chr14:105559299-105559308
50	TCF7L2	chr14:105556801-105558676	HCT-116	colon:	n/a	chr14:105558144-105558160 chr14:105558144-105558160 chr14:105558148-105558158 chr14:105558147-105558156 chr14:105558145-105558159 chr14:105558145-105558159

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105557746-105557796	NHBE	bronchial:	n/a
2	chr14:105557746-105557796	HCPEpiC	choroid plexus:	n/a
3	chr14:105557746-105557796	AG09319	gingival:	n/a
4	chr14:105557746-105557796	AG09309	skin:	n/a
5	chr14:105557746-105557796	MCF-7	breast:	n/a
6	chr14:105557746-105557796	HNPCEpiC	eye:	n/a
7	chr14:105557746-105557796	NT2-D1	testis:	n/a
8	chr14:105557746-105557796	K562	blood:	n/a
9	chr14:105557746-105557796	A549	lung:	n/a
10	chr14:105557746-105557796	GM12892	blood:	n/a
11	chr14:105557746-105557796	AoSMC	blood vessel:	n/a
12	chr14:105557746-105557796	U87	brain:	n/a
13	chr14:105557746-105557796	HepG2	liver:	n/a
14	chr14:105557746-105557796	T-47D	breast:	n/a
15	chr14:105557746-105557796	HPAEpiC	pulmonary alveolar:	n/a
16	chr14:105557746-105557796	HRE	kidney:	n/a
17	chr14:105557746-105557796	HEK293	kidney:	embryo
18	chr14:105557746-105557796	H1-hESC	embryonic stem cell:	embryo
19	chr14:105557746-105557796	Caco-2	colon:	n/a
20	chr14:105557746-105557796	LNCaP	prostate:	n/a
21	chr14:105557746-105557796	MCF10A-Er-Src	breast:	n/a
22	chr14:105557746-105557796	HL-60	blood:	n/a
23	chr14:105557746-105557796	HIPEpiC	eye:	n/a
24	chr14:105557746-105557796	AG04450	lung:	fetal
25	chr14:105557746-105557796	SAEC	small airway:	n/a
26	chr14:105557746-105557796	GM19239	blood:	n/a
27	chr14:105557746-105557796	GM06990	blood:	n/a
28	chr14:105557746-105557796	BJ	skin:	n/a
29	chr14:105557746-105557796	PFSK-1	brain:	n/a
30	chr14:105557746-105557796	Hepatocyte	liver:	n/a
31	chr14:105557746-105557796	AG10803	skin:	n/a
32	chr14:105557746-105557796	AG04449	skin:	fetal
33	chr14:105557746-105557796	NH-A	brain:	n/a
34	chr14:105557746-105557796	GM12891	blood:	n/a
35	chr14:105557746-105557796	CMK	blood:	n/a
36	chr14:105557746-105557796	ProgFib	skin:	n/a
37	chr14:105557746-105557796	HMEC	breast:	n/a
38	chr14:105557746-105557796	GM12878	blood:	n/a
39	chr14:105557746-105557796	NB4	blood:	n/a
40	chr14:105557746-105557796	HCF	heart:	n/a
41	chr14:105557746-105557796	SK-N-SH_RA	brain:	n/a
42	chr14:105557746-105557796	PANC-1	pancreas:	n/a
43	chr14:105557746-105557796	Hela-S3	cervix:	n/a
44	chr14:105557746-105557796	SK-N-MC	brain:	n/a
45	chr14:105557746-105557796	HCT-116	colon:	n/a
46	chr14:105557746-105557796	HUVEC	blood vessel:	n/a
47	chr14:105557746-105557796	ECC-1	luminal epithelium:	n/a
48	chr14:105557746-105557796	ovcar-3	ovarian:	n/a
49	chr14:105557746-105557796	SK-N-SH	brain:	n/a
50	chr14:105557746-105557796	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:105556907..105557905-chr14:105631981..105632717,2	MCF-7	breast:
2	chr14:105478025..105480499-chr14:105557134..105559367,2	MCF-7	breast:
3	chr14:105557263..105559202-chr14:105649515..105651192,2	MCF-7	breast:
4	chr14:105556660..105559437-chr14:105588253..105590015,2	MCF-7	breast:
5	chr14:105555328..105560254-chr14:105631379..105635555,5	MCF-7	breast:
6	chr14:105556861..105558363-chr14:105628903..105631842,2	K562	blood:
7	chr14:105556047..105558699-chr14:105620485..105622825,2	K562	blood:
8	chr14:105556860..105558487-chr14:105603973..105605818,2	K562	blood:
9	chr14:105444294..105445839-chr14:105557247..105559531,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000257556	TF binding region
ENSG00000257556	CpG island
ENSG00000185567	Chromatin interaction
ENSG00000184916	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11844498	1.00[EUR][1000 genomes]
rs2819447	1.00[EUR][1000 genomes]
rs55883015	1.00[EUR][1000 genomes]
rs57499144	1.00[EUR][1000 genomes]
rs57824859	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs59748048	1.00[EUR][1000 genomes]
rs60132793	1.00[EUR][1000 genomes]
rs61433149	1.00[EUR][1000 genomes]
rs74089806	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74089811	1.00[EUR][1000 genomes]
rs74090122	1.00[EUR][1000 genomes]
rs74090125	1.00[EUR][1000 genomes]
rs74090130	1.00[EUR][1000 genomes]
rs74090134	1.00[EUR][1000 genomes]
rs74090136	1.00[EUR][1000 genomes]
rs74090138	1.00[EUR][1000 genomes]
rs74090139	1.00[EUR][1000 genomes]
rs74090141	1.00[EUR][1000 genomes]
rs74090142	1.00[EUR][1000 genomes]
rs74090188	1.00[EUR][1000 genomes]
rs74090193	1.00[EUR][1000 genomes]
rs74090196	1.00[EUR][1000 genomes]
rs74092707	1.00[EUR][1000 genomes]
rs74092713	1.00[EUR][1000 genomes]
rs8017360	1.00[EUR][1000 genomes]
rs8021519	1.00[EUR][1000 genomes]
rs8021521	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	nsv917106	chr14:105339195-105803170	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
5	nsv902421	chr14:105410183-105574843	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer 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	73 gene(s)	inside rSNPs	diseases
6	nsv902422	chr14:105420215-105803170	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
7	nsv1052190	chr14:105423761-105722653	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
8	nsv902423	chr14:105430890-105803170	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
9	nsv1042303	chr14:105435649-105633544	Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
10	nsv456458	chr14:105435649-105690092	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
11	nsv566150	chr14:105435649-105690092	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
12	nsv902424	chr14:105436222-105803170	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS 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	86 gene(s)	inside rSNPs	diseases
13	nsv456459	chr14:105459140-105617891	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
14	nsv566152	chr14:105459140-105617891	Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
15	nsv902425	chr14:105463936-105690092	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
16	nsv9175	chr14:105496509-105688941	Enhancers Strong transcription Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
17	nsv902427	chr14:105508577-105585347	Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer 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	25 gene(s)	inside rSNPs	diseases
18	esv2758369	chr14:105513346-105803170	Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
19	esv2760014	chr14:105513346-105803170	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105551600-105559000	Enhancers	Placenta	Placenta
2	chr14:105554000-105557800	Enhancers	HMEC	breast
3	chr14:105554000-105559000	Enhancers	Gastric	stomach
4	chr14:105554200-105559000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr14:105554200-105559000	Enhancers	Pancreas	Pancrea
6	chr14:105554600-105558400	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr14:105554600-105558600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr14:105554600-105558800	Weak transcription	K562	blood
9	chr14:105554600-105559200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr14:105554800-105557800	Weak transcription	Right Atrium	heart
11	chr14:105554800-105559200	Weak transcription	Primary hematopoietic stem cells	blood
12	chr14:105555400-105557800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr14:105555400-105557800	Weak transcription	NHDF-Ad	bronchial
14	chr14:105555400-105559200	Weak transcription	Ovary	ovary
15	chr14:105555600-105557800	Enhancers	Colonic Mucosa	Colon
16	chr14:105555600-105558000	Flanking Active TSS	A549	lung
17	chr14:105555600-105558400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr14:105555600-105559000	Enhancers	Fetal Muscle Leg	muscle
19	chr14:105555800-105558600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr14:105555800-105559000	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr14:105556000-105559000	Enhancers	Placenta Amnion	Placenta Amnion
22	chr14:105556400-105558200	Enhancers	Muscle Satellite Cultured Cells	--
23	chr14:105556400-105558400	Enhancers	Fetal Intestine Large	intestine
24	chr14:105556400-105559200	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr14:105556400-105559600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr14:105556400-105559800	Enhancers	Spleen	Spleen
27	chr14:105556600-105558200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
28	chr14:105556600-105558600	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr14:105556600-105559000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr14:105556600-105559000	Enhancers	Adipose Nuclei	Adipose
31	chr14:105556600-105559000	Enhancers	Esophagus	oesophagus
32	chr14:105556600-105559000	Enhancers	Fetal Lung	lung
33	chr14:105556600-105559000	Enhancers	Left Ventricle	heart
34	chr14:105556600-105559000	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr14:105556600-105559200	Enhancers	Right Ventricle	heart
36	chr14:105556600-105559800	Enhancers	Fetal Heart	heart
37	chr14:105556800-105558000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr14:105556800-105558000	Enhancers	NHEK	skin
39	chr14:105556800-105558400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr14:105556800-105558400	Enhancers	Duodenum Smooth Muscle	Duodenum
41	chr14:105556800-105558400	Enhancers	Rectal Smooth Muscle	rectum
42	chr14:105556800-105558400	Enhancers	Osteobl	bone
43	chr14:105556800-105558600	Enhancers	Stomach Mucosa	stomach
44	chr14:105556800-105558800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr14:105556800-105558800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr14:105556800-105559000	Weak transcription	Primary B cells from cord blood	blood
47	chr14:105556800-105559000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr14:105556800-105559200	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr14:105556800-105559200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
50	chr14:105556800-105559200	Enhancers	HSMM	muscle

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