Variant report

Variant	esv1850995
Chromosome Location	chr10:696237-735901
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:556)
CpG islands
(count:2994)
Chromatin interactive
region (count:21)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:556 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:727897-728114	HepG2	liver:	n/a	n/a
2	ATF1	chr10:729319-729702	K562	blood:	n/a	n/a
3	BACH1	chr10:734911-735245	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr10:718041-718363	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr10:699656-699670	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr10:723859-724161	GM12878	blood:	n/a	n/a
7	BATF	chr10:705986-706335	GM12878	blood:	n/a	n/a
8	BATF	chr10:722135-722417	GM12878	blood:	n/a	n/a
9	BATF	chr10:722079-722448	GM12878	blood:	n/a	n/a
10	BCL11A	chr10:722144-722453	GM12878	blood:	n/a	n/a
11	BCL11A	chr10:723812-724184	GM12878	blood:	n/a	chr10:723831-723839 chr10:724070-724079 chr10:723932-723945
12	BCL11A	chr10:705958-706431	GM12878	blood:	n/a	n/a
13	BHLHE40	chr10:711494-711760	K562	blood:	n/a	chr10:711672-711681 chr10:711670-711683 chr10:711666-711687 chr10:711558-711571 chr10:711673-711682 chr10:711671-711680 chr10:711672-711681
14	BHLHE40	chr10:695485-697003	HepG2	liver:	n/a	n/a
15	CEBPB	chr10:697228-697554	IMR90	lung:	n/a	n/a
16	CEBPB	chr10:711522-711790	IMR90	lung:	n/a	n/a
17	CEBPB	chr10:735751-735902	HepG2	liver:	n/a	n/a
18	CEBPB	chr10:728114-728118	HepG2	liver:	n/a	n/a
19	CEBPB	chr10:705540-706018	IMR90	lung:	n/a	n/a
20	CEBPB	chr10:733032-733346	IMR90	lung:	n/a	n/a
21	CEBPB	chr10:732595-732615	HepG2	liver:	n/a	n/a
22	CEBPB	chr10:729197-729907	IMR90	lung:	n/a	n/a
23	CEBPD	chr10:695785-696331	HepG2	liver:	n/a	n/a
24	CHD1	chr10:733010-735707	IMR90	lung:	n/a	chr10:735580-735590
25	CHD1	chr10:735773-736854	IMR90	lung:	n/a	n/a
26	CHD1	chr10:734854-734938	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr10:735536-735543	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr10:735449-735952	A549	lung:	n/a	n/a
29	CREB1	chr10:695565-696794	HepG2	liver:	n/a	n/a
30	CREB1	chr10:729206-729742	A549	lung:	n/a	chr10:729479-729492
31	CREB1	chr10:729267-729728	H1-hESC	embryonic stem cell:	n/a	chr10:729479-729492
32	CREB1	chr10:729257-729651	A549	lung:	n/a	chr10:729479-729492
33	CREB1	chr10:729305-729598	K562	blood:	n/a	chr10:729479-729492
34	CTCF	chr10:729660-729810	HAc	cerebellar:	n/a	n/a
35	CTCF	chr10:729692-729716	Gliobla	brain:	n/a	n/a
36	CTCF	chr10:729640-729790	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr10:734280-734430	MCF-7	breast:	n/a	chr10:734372-734385
38	CTCF	chr10:734320-734470	HCPEpiC	choroid plexus:	n/a	chr10:734372-734385
39	CTCF	chr10:700640-700790	AG04450	lung:	n/a	chr10:700699-700708
40	CTCF	chr10:729540-729690	AG04450	lung:	n/a	n/a
41	CTCF	chr10:729740-729890	HFF	foreskin:	n/a	chr10:729807-729820
42	CTCF	chr10:729620-729770	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr10:729640-729790	HMF	breast:	n/a	n/a
44	CTCF	chr10:729680-729830	RPTEC	kidney:	n/a	chr10:729807-729820
45	CTCF	chr10:711558-711749	IMR90	lung:	n/a	n/a
46	CTCF	chr10:729700-729850	AG09319	gingival:	n/a	chr10:729807-729820
47	CTCF	chr10:700580-700730	HepG2	liver:	n/a	chr10:700699-700708
48	CTCF	chr10:729640-729790	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr10:729660-729810	AG04449	skin:	n/a	n/a
50	CTCF	chr10:729420-729570	NHDF-neo	bronchial:	n/a	chr10:729486-729507

(count:2994 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:709610-709660	HCM	heart:	n/a
2	chr10:711944-711994	SK-N-SH_RA	brain:	n/a
3	chr10:716157-716207	HAEpiC	amniotic membrane:	n/a
4	chr10:709898-709948	HCM	heart:	n/a
5	chr10:711897-711947	MCF-7	breast:	n/a
6	chr10:709610-709660	HCM	heart:	n/a
7	chr10:711944-711994	SK-N-SH_RA	brain:	n/a
8	chr10:716157-716207	HAEpiC	amniotic membrane:	n/a
9	chr10:709898-709948	HCM	heart:	n/a
10	chr10:711897-711947	MCF-7	breast:	n/a
11	chr10:729204-729254	CMK	blood:	n/a
12	chr10:709610-709660	NHDF-neo	bronchial:	n/a
13	chr10:717091-717141	AG09309	skin:	n/a
14	chr10:735472-735522	HEEpiC	esophagus:	n/a
15	chr10:735472-735522	PFSK-1	brain:	n/a
16	chr10:711676-711726	RPTEC	kidney:	n/a
17	chr10:709839-709889	HCM	heart:	n/a
18	chr10:729204-729254	HEK293	kidney:	embryo
19	chr10:729479-729529	H1-hESC	embryonic stem cell:	embryo
20	chr10:697901-697951	NHDF-neo	bronchial:	n/a
21	chr10:711676-711726	HAEpiC	amniotic membrane:	n/a
22	chr10:729479-729529	RPTEC	kidney:	n/a
23	chr10:709610-709660	LNCaP	prostate:	n/a
24	chr10:709564-709614	CMK	blood:	n/a
25	chr10:734710-734760	HIPEpiC	eye:	n/a
26	chr10:729204-729254	PFSK-1	brain:	n/a
27	chr10:729001-729051	HCF	heart:	n/a
28	chr10:697840-697890	HCPEpiC	choroid plexus:	n/a
29	chr10:708425-708475	SKMC	muscle:	n/a
30	chr10:709564-709614	AG09309	skin:	n/a
31	chr10:709839-709889	ovcar-3	ovarian:	n/a
32	chr10:724510-724560	AG09319	gingival:	n/a
33	chr10:734710-734760	HRCEpiC	kidney:	n/a
34	chr10:731292-731342	U87	brain:	n/a
35	chr10:726822-726872	BE2_C	brain:	n/a
36	chr10:706006-706056	HNPCEpiC	eye:	n/a
37	chr10:709610-709660	GM12891	blood:	n/a
38	chr10:717091-717141	NB4	blood:	n/a
39	chr10:734399-734449	H1-hESC	embryonic stem cell:	embryo
40	chr10:697771-697821	HCT-116	colon:	n/a
41	chr10:734710-734760	T-47D	breast:	n/a
42	chr10:734268-734318	HNPCEpiC	eye:	n/a
43	chr10:729001-729051	Caco-2	colon:	n/a
44	chr10:697055-697105	K562	blood:	n/a
45	chr10:729204-729254	IMR90	lung:	fetal
46	chr10:729204-729254	AG09319	gingival:	n/a
47	chr10:712592-712642	HIPEpiC	eye:	n/a
48	chr10:729226-729276	HEEpiC	esophagus:	n/a
49	chr10:697055-697105	BE2_C	brain:	n/a
50	chr10:698258-698308	AG10803	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:735855..737615-chr10:818949..821134,2	MCF-7	breast:
2	chr10:723887..725590-chr10:731403..733656,2	MCF-7	breast:
3	chr10:725778..731472-chr10:731586..738263,11	MCF-7	breast:
4	chr10:723887..725590-chr10:731403..733656,2	MCF-7	breast:
5	chr10:701409..702201-chr19:4341065..4341565,2	MCF-7	breast:
6	chr10:705629..708619-chr10:732652..734638,2	MCF-7	breast:
7	chr10:719611..721837-chr10:748749..751307,2	K562	blood:
8	chr10:733710..735507-chr10:754476..756731,2	MCF-7	breast:
9	chr10:656339..658937-chr10:722531..724771,2	MCF-7	breast:
10	chr10:687008..688714-chr10:699568..702258,2	MCF-7	breast:
11	chr10:705629..708619-chr10:732652..734638,2	MCF-7	breast:
12	chr10:717115..720273-chr10:724564..727281,3	MCF-7	breast:
13	chr10:698785..701781-chr10:833421..835495,2	MCF-7	breast:
14	chr10:721854..725155-chr10:733736..736400,3	MCF-7	breast:
15	chr10:674481..678808-chr10:734028..737251,4	MCF-7	breast:
16	chr10:583403..585208-chr10:714450..715956,2	K562	blood:
17	chr10:692009..694331-chr10:706518..708449,2	MCF-7	breast:
18	chr10:603209..605062-chr10:710188..713086,2	MCF-7	breast:
19	chr10:712816..715288-chr10:723469..725023,2	MCF-7	breast:
20	chr10:692996..695820-chr10:700101..701896,2	MCF-7	breast:
21	chr10:717115..720273-chr10:724564..727281,3	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf108-1	chr10:697051-698595	NONHSAT010867
2	lnc-LARP4B-3	chr10:724395-724591	NONHSAT010869
3	lnc-C10orf108-1	chr10:712158-712562	ENSG00000242357.1
4	lnc-LARP4B-3	chr10:724715-724736	NONHSAT010869
5	lnc-C10orf108-5	chr10:714400-715521	ENSG00000272992.1
6	lnc-C10orf108-1	chr10:707966-708058	NR_027152
7	lnc-C10orf108-1	chr10:708731-711109	NR_027152
8	lnc-C10orf108-1	chr10:696017-696382	NR_027152
9	lnc-C10orf108-1	chr10:709498-709642	ENSG00000242357.1
10	lnc-C10orf108-1	chr10:696231-696382	NONHSAT010867

No data

Variant related genes	Relation type
ENSG00000242357	TF binding region
DIP2C	TF binding region
ENSG00000272992	TF binding region
ENSG00000242357	CpG island
DIP2C	CpG island
ENSG00000272992	CpG island
ENSG00000272992	chromatin interactions
ENSG00000151240	chromatin interactions
ENSG00000225140	chromatin interactions
ENSG00000263511	chromatin interactions

Extended variants
information (count: 1882 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1882 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10904535	chr10:696237-696238	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184617249	chr10:696265-696266	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
3	rs143209427	chr10:696269-696270	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
4	rs546369681	chr10:696293-696294	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
5	rs566375861	chr10:696297-696298	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
6	rs187635206	chr10:696311-696312	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
7	rs375788699	chr10:696322-696323	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
8	rs565810003	chr10:696347-696348	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
9	rs575248445	chr10:696348-696349	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
10	rs537817244	chr10:696361-696362	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
11	rs554281573	chr10:696366-696367	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
12	rs370371589	chr10:696371-696372	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
13	rs540953472	chr10:696376-696377	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
14	rs560661756	chr10:696394-696395	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs192155114	chr10:696429-696430	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546425502	chr10:696451-696452	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562975230	chr10:696456-696457	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531728154	chr10:696470-696471	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs369977198	chr10:696480-696481	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548547445	chr10:696566-696567	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561968746	chr10:696592-696593	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529936221	chr10:696593-696594	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184197857	chr10:696600-696601	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566437475	chr10:696617-696618	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs368014786	chr10:696634-696635	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs371096058	chr10:696660-696661	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs551363168	chr10:696669-696670	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs571244431	chr10:696671-696672	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs552108075	chr10:696672-696673	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs117202400	chr10:696673-696674	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs372488998	chr10:696678-696679	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs188547195	chr10:696704-696705	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs568008777	chr10:696780-696781	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs533780568	chr10:696782-696783	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs371962877	chr10:696798-696799	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs556825935	chr10:696827-696828	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs577637683	chr10:696838-696839	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs375589422	chr10:696839-696840	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs556514778	chr10:696865-696866	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs199557839	chr10:696869-696870	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs115626395	chr10:696873-696874	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs542006019	chr10:696888-696889	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs562103071	chr10:696909-696910	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs527639031	chr10:696910-696911	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs541030235	chr10:696925-696926	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs559987801	chr10:696935-696936	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs368947867	chr10:696936-696937	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs199865334	chr10:696970-696971	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs370122680	chr10:697083-697084	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs576709184	chr10:697090-697091	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD
Obesity	19966786	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1790 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:672000-700000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr10:684200-700000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr10:685600-699800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr10:687400-700000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr10:688800-698200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr10:688800-702600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr10:691200-704200	Weak transcription	HSMM	muscle
8	chr10:691200-704800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr10:691400-704200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr10:694600-696400	Weak transcription	Esophagus	oesophagus
11	chr10:694600-696400	Weak transcription	Spleen	Spleen
12	chr10:695000-697800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr10:695200-696400	Enhancers	Brain Substantia Nigra	brain
14	chr10:695200-697200	Enhancers	Fetal Lung	lung
15	chr10:695400-696400	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr10:695400-696600	Enhancers	Fetal Brain Female	brain
17	chr10:695600-696400	Enhancers	Brain Anterior Caudate	brain
18	chr10:695600-696600	Active TSS	Duodenum Mucosa	Duodenum
19	chr10:695600-696600	Flanking Active TSS	A549	lung
20	chr10:695600-696800	Enhancers	Fetal Heart	heart
21	chr10:695600-697000	Flanking Active TSS	Stomach Mucosa	stomach
22	chr10:695600-697200	Active TSS	Aorta	Aorta
23	chr10:695600-697200	Active TSS	Liver	Liver
24	chr10:695600-697400	Flanking Active TSS	Rectal Smooth Muscle	rectum
25	chr10:695600-697400	Flanking Active TSS	HepG2	liver
26	chr10:695600-698000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
27	chr10:695600-698400	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr10:695600-699200	Enhancers	Fetal Brain Male	brain
29	chr10:695800-696400	Flanking Active TSS	Stomach Smooth Muscle	stomach
30	chr10:695800-696400	Flanking Active TSS	NHLF	lung
31	chr10:695800-696600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr10:695800-696600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
33	chr10:695800-696800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr10:695800-696800	Active TSS	Duodenum Smooth Muscle	Duodenum
35	chr10:695800-696800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
36	chr10:695800-697000	Flanking Active TSS	Adipose Nuclei	Adipose
37	chr10:695800-697000	Flanking Active TSS	Brain Hippocampus Middle	brain
38	chr10:695800-697200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr10:695800-697400	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr10:695800-697600	Enhancers	Lung	lung
41	chr10:695800-698800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr10:695800-699000	Enhancers	Fetal Muscle Leg	muscle
43	chr10:695800-699200	Enhancers	Fetal Muscle Trunk	muscle
44	chr10:696000-696400	Flanking Active TSS	Colon Smooth Muscle	Colon
45	chr10:696000-696400	Flanking Active TSS	Fetal Intestine Small	intestine
46	chr10:696000-696400	Flanking Active TSS	Psoas Muscle	Psoas
47	chr10:696000-696600	Active TSS	Gastric	stomach
48	chr10:696000-696800	Flanking Active TSS	Ovary	ovary
49	chr10:696000-697000	Flanking Active TSS	Fetal Intestine Large	intestine
50	chr10:696000-697000	Flanking Active TSS	Fetal Stomach	stomach

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