Variant report

Variant	rs598300
Chromosome Location	chr18:269728-269729
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:21)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:21 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr18:269527-270093	MCF10A-Er-Src	breast:	n/a	n/a
2	RXRA	chr18:269514-269820	HepG2	liver:	n/a	n/a
3	CEBPB	chr18:269678-269795	K562	blood:	n/a	n/a
4	POLR2A	chr18:267450-269926	HepG2	liver:	n/a	n/a
5	FOXA1	chr18:269361-269746	HepG2	liver:	n/a	n/a
6	CEBPB	chr18:269538-269869	K562	blood:	n/a	n/a
7	POLR2A	chr18:269523-270062	MCF10A-Er-Src	breast:	n/a	n/a
8	FOXA1	chr18:269398-269920	HepG2	liver:	n/a	n/a
9	POLR2A	chr18:267395-269856	HepG2	liver:	n/a	n/a
10	EP300	chr18:269692-269744	K562	blood:	n/a	n/a
11	NFIC	chr18:269453-269916	HepG2	liver:	n/a	n/a
12	POLR2A	chr18:267238-269847	SK-N-MC	brain:	n/a	n/a
13	POLR2A	chr18:269422-270195	K562	blood:	n/a	n/a
14	FOXA2	chr18:269382-269802	HepG2	liver:	n/a	n/a
15	ARID3A	chr18:269422-269886	HepG2	liver:	n/a	n/a
16	HDAC2	chr18:269538-269853	HepG2	liver:	n/a	n/a
17	FOXA1	chr18:269386-269771	HepG2	liver:	n/a	n/a
18	RCOR1	chr18:269591-269783	K562	blood:	n/a	n/a
19	NFIC	chr18:269480-269821	HepG2	liver:	n/a	n/a
20	MYBL2	chr18:269380-269910	HepG2	liver:	n/a	n/a
21	MYBL2	chr18:269434-269900	HepG2	liver:	n/a	n/a

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:254095..260758-chr18:263922..270842,11	K562	blood:
2	chr17:58235617..58237608-chr18:268202..269943,2	MCF-7	breast:
3	chr18:269454..272332-chr18:624341..626546,2	K562	blood:
4	chr18:257542..263185-chr18:266000..270349,8	MCF-7	breast:
5	chr18:269653..272578-chr18:297355..299675,2	K562	blood:
6	chr18:229127..231742-chr18:269257..272237,2	K562	blood:
7	chr18:245734..247470-chr18:268204..270574,2	K562	blood:
8	chr18:268277..271095-chr18:349761..352127,2	K562	blood:
9	chr18:269547..271961-chr18:280130..281760,2	K562	blood:
10	chr18:158336..160794-chr18:268769..270393,2	K562	blood:
11	chr18:251595..253868-chr18:269090..271217,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP14-3	chr18:268148-270278	ENSG00000263884.1

No data

Variant related genes	Relation type
THOC1	TF binding region
ENSG00000079101	Chromatin interaction
ENSG00000101557	Chromatin interaction
ENSG00000079134	Chromatin interaction

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1299113	0.86[ASN][1000 genomes]
rs1784380	0.81[ASN][1000 genomes]
rs1785049	0.81[ASN][1000 genomes]
rs2509447	0.81[ASN][1000 genomes]
rs471274	0.84[ASN][1000 genomes]
rs481077	0.91[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.90[YRI][hapmap];0.82[AFR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs513402	0.84[ASN][1000 genomes]
rs513894	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs514003	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs523239	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs535992	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs545447	0.86[ASN][1000 genomes]
rs545684	1.00[ASW][hapmap];0.92[LWK][hapmap];0.85[YRI][hapmap]
rs546590	0.85[ASN][1000 genomes]
rs577454	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs579219	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs580453	0.85[ASN][1000 genomes]
rs585578	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs599361	0.80[EUR][1000 genomes]
rs600022	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.95[JPT][hapmap];0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs600220	1.00[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs605826	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs620380	0.87[CHB][hapmap];0.81[ASN][1000 genomes]
rs620837	0.87[CHB][hapmap];0.81[ASN][1000 genomes]
rs620970	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs621782	1.00[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs631152	0.85[ASN][1000 genomes]
rs631343	1.00[CEU][hapmap];0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs644438	0.96[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.91[JPT][hapmap];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs655781	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs663186	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs672856	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs681624	0.83[ASN][1000 genomes]
rs7238463	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1061730	chr18:11543-322183	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv1059645	chr18:11543-326679	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv576227	chr18:52933-322183	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv1064150	chr18:99036-321710	Genic enhancers Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
5	nsv1055303	chr18:112328-304352	Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
6	nsv543527	chr18:112328-304352	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
7	nsv543530	chr18:112528-932674	Weak transcription Strong transcription Bivalent Enhancer Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
8	nsv1067102	chr18:112528-984688	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
9	nsv543531	chr18:112528-984688	Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer 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	83 gene(s)	inside rSNPs	diseases
10	nsv1057029	chr18:141491-356238	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
11	nsv1066995	chr18:141491-415027	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
12	nsv1064735	chr18:141491-483651	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
13	nsv1062680	chr18:141491-549166	Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
14	nsv1067218	chr18:141491-603796	Weak transcription Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
15	nsv543544	chr18:141491-675519	Bivalent/Poised TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active 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	56 gene(s)	inside rSNPs	diseases
16	nsv1064998	chr18:141491-1095845	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
17	nsv543545	chr18:141491-1095845	Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
18	nsv531216	chr18:148763-293736	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
19	nsv532441	chr18:148763-1108997	Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
20	nsv530373	chr18:148963-533693	Weak transcription Strong transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
21	nsv482910	chr18:161390-305010	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
22	nsv518642	chr18:196829-331506	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
23	nsv1067432	chr18:219990-290812	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
24	nsv948987	chr18:220071-461872	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
25	nsv948735	chr18:220071-615394	Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
26	nsv915747	chr18:225017-287764	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
27	nsv534315	chr18:225061-776966	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
28	nsv909287	chr18:225964-677240	Genic enhancers Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
29	nsv1056707	chr18:231508-290812	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
30	nsv2174	chr18:240074-285087	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
31	nsv1060428	chr18:252297-322289	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer 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	14 gene(s)	inside rSNPs	diseases
32	nsv543561	chr18:252297-322289	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent Enhancer Genic enhancers 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	14 gene(s)	inside rSNPs	diseases
33	nsv1058796	chr18:254290-313208	Enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
34	nsv543562	chr18:254290-313208	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
35	nsv1066129	chr18:258717-369148	Strong transcription Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer 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 target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:267000-270000	Active TSS	HUES64 Cell Line	embryonic stem cell
2	chr18:267600-270200	Active TSS	Duodenum Smooth Muscle	Duodenum
3	chr18:268800-269800	Flanking Active TSS	Liver	Liver
4	chr18:268800-269800	Flanking Active TSS	GM12878-XiMat	blood
5	chr18:269000-269800	Enhancers	Primary hematopoietic stem cells	blood
6	chr18:269000-269800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr18:269000-269800	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr18:269000-270000	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr18:269000-270000	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr18:269000-270200	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr18:269000-272600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr18:269200-269800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr18:269200-269800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr18:269200-269800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr18:269200-269800	Enhancers	Brain Anterior Caudate	brain
16	chr18:269200-269800	Enhancers	Brain Cingulate Gyrus	brain
17	chr18:269200-269800	Enhancers	Brain Hippocampus Middle	brain
18	chr18:269200-269800	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr18:269200-269800	Enhancers	Brain Substantia Nigra	brain
20	chr18:269200-269800	Enhancers	Fetal Lung	lung
21	chr18:269200-269800	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr18:269200-270000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr18:269200-270000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr18:269200-270000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr18:269200-270000	Enhancers	Primary T killer memory cells from peripheral blood	blood
26	chr18:269200-270000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr18:269200-270000	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr18:269200-270000	Enhancers	A549	lung
29	chr18:269200-270200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr18:269200-270200	Enhancers	Dnd41	blood
31	chr18:269200-271600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr18:269200-272400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr18:269200-272600	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr18:269200-275600	Weak transcription	Right Atrium	heart
35	chr18:269200-276200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr18:269400-269800	Flanking Active TSS	Fetal Intestine Small	intestine
37	chr18:269400-269800	Enhancers	Stomach Smooth Muscle	stomach
38	chr18:269400-269800	Flanking Active TSS	HepG2	liver
39	chr18:269400-269800	Transcr. at gene 5' and 3'	K562	blood
40	chr18:269400-270200	Enhancers	H1 Cell Line	embryonic stem cell
41	chr18:269400-270200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr18:269400-270200	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr18:269400-271000	Enhancers	Fetal Intestine Large	intestine
44	chr18:269400-271800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr18:269600-269800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr18:269600-269800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
47	chr18:269600-269800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
48	chr18:269600-269800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr18:269600-269800	Flanking Active TSS	Duodenum Mucosa	Duodenum
50	chr18:269600-269800	Flanking Active TSS	Fetal Kidney	kidney

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