Variant report

Variant	nsv1047289
Chromosome Location	chr10:43454528-43487986
allele	n/a
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	ATF1	chr10:43474055-43474377	K562	blood:	n/a	n/a
2	ATF1	chr10:43474747-43475125	K562	blood:	n/a	n/a
3	BACH1	chr10:43455879-43456257	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr10:43455972-43456235	GM12878	blood:	n/a	n/a
5	BHLHE40	chr10:43484487-43484837	K562	blood:	n/a	n/a
6	BHLHE40	chr10:43476829-43477169	K562	blood:	n/a	chr10:43476970-43476986
7	CCNT2	chr10:43476863-43477053	K562	blood:	n/a	n/a
8	CEBPB	chr10:43477134-43477208	K562	blood:	n/a	n/a
9	CEBPB	chr10:43456810-43457012	K562	blood:	n/a	chr10:43456929-43456938 chr10:43456928-43456939 chr10:43456927-43456938
10	CEBPB	chr10:43456763-43457109	IMR90	lung:	n/a	chr10:43456929-43456938 chr10:43456928-43456939 chr10:43456927-43456938
11	CEBPB	chr10:43456879-43457110	Hela-S3	cervix:	n/a	chr10:43456929-43456938 chr10:43456928-43456939 chr10:43456927-43456938
12	CEBPB	chr10:43467355-43467475	IMR90	lung:	n/a	n/a
13	CEBPB	chr10:43456772-43457109	A549	lung:	n/a	chr10:43456929-43456938 chr10:43456928-43456939 chr10:43456927-43456938
14	CEBPB	chr10:43468559-43468690	K562	blood:	n/a	chr10:43468625-43468636 chr10:43468624-43468637
15	CEBPB	chr10:43468469-43468786	HepG2	liver:	n/a	chr10:43468625-43468636 chr10:43468624-43468637
16	CEBPB	chr10:43456758-43457107	HepG2	liver:	n/a	chr10:43456929-43456938 chr10:43456928-43456939 chr10:43456927-43456938
17	CEBPB	chr10:43474862-43474980	K562	blood:	n/a	n/a
18	CHD2	chr10:43471209-43471243	HepG2	liver:	n/a	n/a
19	CTCF	chr10:43475300-43475530	BE2_C	brain:	n/a	n/a
20	CTCF	chr10:43471200-43471350	GM06990	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
21	CTCF	chr10:43470960-43471606	A549	lung:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
22	CTCF	chr10:43471320-43471470	A549	lung:	n/a	n/a
23	CTCF	chr10:43471320-43471470	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr10:43471200-43471350	K562	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
25	CTCF	chr10:43455973-43456063	MCF-7	breast:	n/a	n/a
26	CTCF	chr10:43471160-43471310	GM12870	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
27	CTCF	chr10:43471160-43471310	HepG2	liver:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
28	CTCF	chr10:43471200-43471350	HepG2	liver:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
29	CTCF	chr10:43471156-43471370	Hela-S3	cervix:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
30	CTCF	chr10:43471072-43471434	K562	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
31	CTCF	chr10:43471193-43471318	GM19239	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
32	CTCF	chr10:43471129-43471397	Gliobla	brain:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
33	CTCF	chr10:43457940-43458090	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr10:43471144-43471346	A549	lung:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
35	CTCF	chr10:43457220-43457370	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr10:43471192-43471328	GM19238	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
37	CTCF	chr10:43475360-43475510	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr10:43455971-43456059	NHEK	skin:	n/a	n/a
39	CTCF	chr10:43471180-43471330	WERI-Rb-1	eye:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
40	CTCF	chr10:43471180-43471330	AG04449	skin:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
41	CTCF	chr10:43471180-43471330	BE2_C	brain:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
42	CTCF	chr10:43471001-43471519	K562	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
43	CTCF	chr10:43471230-43471289	LNCaP	prostate:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
44	CTCF	chr10:43471200-43471350	Hela-S3	cervix:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
45	CTCF	chr10:43471163-43471345	GM12878	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
46	CTCF	chr10:43471180-43471329	ProgFib	skin:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
47	CTCF	chr10:43471040-43471190	GM12869	blood:	n/a	n/a
48	CTCF	chr10:43471134-43471359	H1-hESC	embryonic stem cell:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
49	CTCF	chr10:43471240-43471390	Caco-2	colon:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
50	CTCF	chr10:43471073-43471350	T-47D	breast:	n/a	chr10:43471275-43471283 chr10:43471268-43471286

No.	Distal block	Cell Line	Cell type
1	chr10:43454488..43457151-chr10:43458866..43460532,2	K562	blood:
2	chr10:43454488..43457151-chr10:43458866..43460532,2	K562	blood:
3	chr10:43361913..43362690-chr10:43470789..43471679,3	MCF-7	breast:
4	chr10:43477135..43480872-chr10:43482623..43485089,4	MCF-7	breast:
5	chr10:43482866..43485744-chr10:43490374..43493373,2	K562	blood:
6	chr10:43481086..43483555-chr10:43520776..43523098,2	MCF-7	breast:
7	chr10:43442278..43444933-chr10:43480874..43482921,2	K562	blood:
8	chr10:43472744..43475645-chr10:43482853..43485433,2	K562	blood:
9	chr10:43469169..43471779-chr10:43471792..43473949,2	K562	blood:
10	chr10:43454969..43457476-chr10:43464603..43467508,2	MCF-7	breast:
11	chr10:43465926..43467640-chr10:43469651..43471316,2	K562	blood:
12	chr10:43486095..43489357-chr10:43490017..43492485,3	MCF-7	breast:
13	chr10:43448104..43449836-chr10:43453416..43456002,2	MCF-7	breast:
14	chr10:43365868..43366659-chr10:43470638..43471752,5	MCF-7	breast:
15	chr10:43469169..43471779-chr10:43471792..43473949,2	K562	blood:
16	chr10:43450805..43453524-chr10:43455350..43458252,2	MCF-7	breast:
17	chr10:43472378..43475581-chr10:43520718..43522410,3	MCF-7	breast:
18	chr10:43471587..43474099-chr10:43476210..43479281,3	MCF-7	breast:
19	chr10:43471183..43472148-chr4:106629910..106630418,2	NB4	blood:
20	chr10:43361871..43362799-chr10:43470867..43471733,6	MCF-7	breast:
21	chr10:43458559..43459070-chr17:7387320..7387822,2	NB4	blood:
22	chr10:43471330..43471857-chr3:38035458..38036022,2	NB4	blood:
23	chr10:43472048..43472812-chr11:819441..820070,2	NB4	blood:
24	chr10:43487519..43490099-chr10:43491819..43493663,2	MCF-7	breast:
25	chr10:43477135..43480872-chr10:43482623..43485089,4	MCF-7	breast:
26	chr10:43470043..43470710-chr4:7069530..7070337,2	NB4	blood:
27	chr10:43369343..43371320-chr10:43469616..43472165,2	MCF-7	breast:
28	chr10:43471160..43472154-chr11:102217419..102218246,2	NB4	blood:
29	chr10:43450142..43452389-chr10:43455226..43458611,3	K562	blood:
30	chr10:43465926..43467640-chr10:43469651..43471316,2	K562	blood:
31	chr10:43452048..43454806-chr10:43520323..43522084,2	MCF-7	breast:
32	chr10:43463562..43467082-chr10:43469575..43473842,3	MCF-7	breast:
33	chr10:43457137..43457637-chr11:95522694..95523216,2	NB4	blood:
34	chr10:43474536..43476774-chr10:43520389..43522895,3	MCF-7	breast:
35	chr10:43470988..43471723-chr10:43574194..43574824,2	MCF-7	breast:
36	chr1:113932116..113933106-chr10:43470154..43470896,2	NB4	blood:
37	chr10:43484291..43485932-chr10:43488466..43491187,2	MCF-7	breast:
38	chr10:43463562..43467082-chr10:43469575..43473842,3	MCF-7	breast:
39	chr10:43454448..43456264-chr10:43474294..43477157,2	MCF-7	breast:
40	chr10:43469610..43472857-chr10:43520371..43524809,5	MCF-7	breast:
41	chr10:43361867..43362389-chr10:43470791..43471531,2	K562	blood:
42	chr10:43474227..43476529-chr10:43479652..43481353,2	MCF-7	breast:
43	chr10:43454969..43457476-chr10:43464603..43467508,2	MCF-7	breast:
44	chr10:43467866..43472352-chr10:43571131..43575180,5	MCF-7	breast:
45	chr10:43474227..43476529-chr10:43479652..43481353,2	MCF-7	breast:
46	chr10:43472744..43475645-chr10:43482853..43485433,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RET-3	chr10:43487172-43487532	ucscGeneNc_uc001jba_2
2	lnc-RET-3	chr10:43486575-43486975	ucscGeneNc_uc001jba_2
3	lnc-RET-2	chr10:43482124-43482459	NONHSAT012938
4	lnc-RET-2	chr10:43481122-43481247	NONHSAT012938
5	lnc-RET-3	chr10:43487762-43487899	ucscGeneNc_uc001jba_2
6	lnc-RASGEF1A-1	chr10:43474465-43474547	XLOC_008790
7	lnc-RASGEF1A-1	chr10:43476816-43476955	XLOC_008790
8	lnc-RASGEF1A-1	chr10:43475731-43476007	XLOC_008790

Variant related genes	Relation type
ENSG00000229630	TF binding region
ENSG00000136059	chromatin interactions
ENSG00000165731	chromatin interactions
ENSG00000229630	chromatin interactions
ENSG00000110330	chromatin interactions
ENSG00000138780	chromatin interactions
ENSG00000138785	chromatin interactions
ENSG00000166037	chromatin interactions
ENSG00000077458	chromatin interactions
ENSG00000174282	chromatin interactions
ENSG00000181222	chromatin interactions
ENSG00000109519	chromatin interactions
ENSG00000263795	chromatin interactions

Extended variants
information (count: 1428 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1428 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371650035	chr10:43454537-43454538	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs149545042	chr10:43454561-43454562	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs534096830	chr10:43454598-43454599	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs35614881	chr10:43454606-43454607	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553224150	chr10:43454624-43454625	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs531807163	chr10:43454653-43454654	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs577964303	chr10:43454673-43454674	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs550124679	chr10:43454723-43454724	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs568674067	chr10:43454745-43454746	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs538932477	chr10:43454754-43454755	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs535651643	chr10:43454756-43454757	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs547732128	chr10:43454799-43454800	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs566023097	chr10:43454852-43454853	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs556673554	chr10:43454899-43454900	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs558101529	chr10:43454927-43454928	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs576879580	chr10:43455062-43455063	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs75827370	chr10:43455112-43455113	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs555961840	chr10:43455114-43455115	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs367695713	chr10:43455162-43455163	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs114395361	chr10:43455171-43455172	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs191048845	chr10:43455248-43455249	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs560467367	chr10:43455263-43455264	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs572325184	chr10:43455272-43455273	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs546245418	chr10:43455306-43455307	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs947696	chr10:43455339-43455340	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs542248862	chr10:43455346-43455347	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs543924809	chr10:43455383-43455384	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs144156350	chr10:43455387-43455388	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs561204742	chr10:43455440-43455441	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs562131364	chr10:43455468-43455469	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs529486045	chr10:43455469-43455470	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs183355262	chr10:43455479-43455480	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs139955535	chr10:43455533-43455534	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs144208625	chr10:43455543-43455544	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs112285469	chr10:43455550-43455551	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs551641260	chr10:43455565-43455566	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs572626091	chr10:43455589-43455590	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs570454329	chr10:43455661-43455662	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs1815722	chr10:43455687-43455688	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs556263572	chr10:43455724-43455725	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs559533293	chr10:43455798-43455799	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs548112630	chr10:43455804-43455805	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs535647012	chr10:43455856-43455857	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs140103405	chr10:43455857-43455858	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs111979500	chr10:43455858-43455859	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs9703651	chr10:43455860-43455861	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs111435737	chr10:43455899-43455900	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs572389409	chr10:43455900-43455901	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs546155614	chr10:43455908-43455909	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs376318197	chr10:43455919-43455920	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:234 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43447600-43455800	Weak transcription	Left Ventricle	heart
2	chr10:43448600-43456200	Weak transcription	Right Ventricle	heart
3	chr10:43453000-43455800	Weak transcription	HSMMtube	muscle
4	chr10:43453400-43459200	Enhancers	Fetal Muscle Leg	muscle
5	chr10:43454400-43455000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr10:43454600-43454800	Weak transcription	Psoas Muscle	Psoas
7	chr10:43454800-43455000	Enhancers	Psoas Muscle	Psoas
8	chr10:43454800-43458600	Enhancers	Spleen	Spleen
9	chr10:43454800-43458800	Enhancers	Fetal Muscle Trunk	muscle
10	chr10:43455000-43455800	Weak transcription	Psoas Muscle	Psoas
11	chr10:43455200-43457600	Enhancers	HMEC	breast
12	chr10:43455400-43456600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr10:43455400-43457400	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr10:43455400-43457600	Enhancers	NHEK	skin
15	chr10:43455600-43456800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr10:43455600-43458000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr10:43455800-43456400	Enhancers	Muscle Satellite Cultured Cells	--
18	chr10:43455800-43456400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr10:43455800-43456600	Enhancers	HSMMtube	muscle
20	chr10:43455800-43457000	Enhancers	HSMM	muscle
21	chr10:43455800-43458000	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr10:43455800-43458400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr10:43455800-43458400	Enhancers	Placenta	Placenta
24	chr10:43455800-43458600	Enhancers	Left Ventricle	heart
25	chr10:43455800-43458600	Enhancers	Psoas Muscle	Psoas
26	chr10:43455800-43458600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
27	chr10:43455800-43460200	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr10:43456000-43456400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr10:43456000-43458200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr10:43456000-43458600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr10:43456000-43458600	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr10:43456200-43456600	Enhancers	H1 Cell Line	embryonic stem cell
33	chr10:43456200-43457800	Enhancers	Right Atrium	heart
34	chr10:43456200-43458400	Enhancers	Right Ventricle	heart
35	chr10:43456400-43456600	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr10:43456400-43457000	Enhancers	Pancreas	Pancrea
37	chr10:43456400-43457400	Enhancers	Fetal Stomach	stomach
38	chr10:43456400-43457600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr10:43456400-43459400	Enhancers	Adipose Nuclei	Adipose
40	chr10:43456600-43457000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr10:43456600-43457000	Weak transcription	HSMMtube	muscle
42	chr10:43456600-43461800	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr10:43456800-43458000	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr10:43456800-43459000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr10:43457000-43457200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr10:43457000-43457400	Enhancers	HSMMtube	muscle
47	chr10:43457200-43458200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr10:43457200-43458200	Enhancers	Fetal Lung	lung
49	chr10:43457400-43457600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
50	chr10:43457400-43458200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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