Variant report

Variant	nsv1015997
Chromosome Location	chr5:76079720-76129241
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1825)
CpG islands
(count:1527)
Chromatin interactive
region (count:20)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1825 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:76114553-76114860	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:76126576-76126776	K562	blood:	n/a	n/a
3	ARID3A	chr5:76083060-76083212	K562	blood:	n/a	n/a
4	ARID3A	chr5:76086428-76087095	K562	blood:	n/a	n/a
5	ARID3A	chr5:76081436-76081712	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:76116209-76116734	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:76086368-76087004	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:76101782-76102245	K562	blood:	n/a	n/a
9	ARID3A	chr5:76113989-76114292	HepG2	liver:	n/a	n/a
10	ATF1	chr5:76086458-76087131	K562	blood:	n/a	n/a
11	ATF1	chr5:76101722-76102174	K562	blood:	n/a	n/a
12	ATF2	chr5:76113947-76114568	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr5:76126912-76127331	GM12878	blood:	n/a	n/a
14	ATF2	chr5:76114079-76115052	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr5:76086364-76086842	GM12878	blood:	n/a	n/a
16	ATF2	chr5:76103843-76104561	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr5:76126950-76127363	GM12878	blood:	n/a	n/a
18	ATF2	chr5:76103823-76104436	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr5:76101627-76102562	A549	lung:	n/a	n/a
20	ATF3	chr5:76081264-76081700	A549	lung:	n/a	n/a
21	ATF3	chr5:76081235-76081754	A549	lung:	n/a	n/a
22	ATF3	chr5:76086335-76086970	A549	lung:	n/a	n/a
23	ATF3	chr5:76114447-76115003	A549	lung:	n/a	chr5:76114977-76114986 chr5:76114862-76114870
24	ATF3	chr5:76100044-76100672	A549	lung:	n/a	n/a
25	ATF3	chr5:76099975-76100655	A549	lung:	n/a	n/a
26	ATF3	chr5:76086333-76087061	A549	lung:	n/a	n/a
27	ATF3	chr5:76101689-76102467	A549	lung:	n/a	n/a
28	ATF3	chr5:76086822-76087094	K562	blood:	n/a	n/a
29	ATF3	chr5:76114432-76115010	A549	lung:	n/a	chr5:76114977-76114986 chr5:76114862-76114870
30	BACH1	chr5:76103704-76103712	K562	blood:	n/a	n/a
31	BACH1	chr5:76114200-76116153	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr5:76126596-76126774	K562	blood:	n/a	n/a
33	BATF	chr5:76126956-76127325	GM12878	blood:	n/a	n/a
34	BATF	chr5:76086433-76086741	GM12878	blood:	n/a	chr5:76086559-76086569
35	BATF	chr5:76086446-76086954	GM12878	blood:	n/a	chr5:76086559-76086569
36	BATF	chr5:76102000-76102358	GM12878	blood:	n/a	n/a
37	BCL11A	chr5:76126997-76127227	GM12878	blood:	n/a	chr5:76127105-76127114
38	BCL11A	chr5:76086438-76086837	GM12878	blood:	n/a	n/a
39	BCL11A	chr5:76126931-76127279	GM12878	blood:	n/a	chr5:76127105-76127114
40	BCL11A	chr5:76086459-76086753	GM12878	blood:	n/a	n/a
41	BCL3	chr5:76101399-76102582	A549	lung:	n/a	chr5:76102262-76102271
42	BCL3	chr5:76101972-76102349	GM12878	blood:	n/a	chr5:76102262-76102271
43	BCL3	chr5:76081377-76081777	A549	lung:	n/a	n/a
44	BCL3	chr5:76109782-76110506	A549	lung:	n/a	chr5:76110348-76110357
45	BCL3	chr5:76097061-76097862	A549	lung:	n/a	n/a
46	BCL3	chr5:76126569-76127455	A549	lung:	n/a	chr5:76127105-76127114
47	BCL3	chr5:76126827-76127402	A549	lung:	n/a	chr5:76127105-76127114
48	BCL3	chr5:76126983-76127322	GM12878	blood:	n/a	chr5:76127105-76127114
49	BCL3	chr5:76081199-76081823	A549	lung:	n/a	n/a
50	BCL3	chr5:76101545-76102516	A549	lung:	n/a	chr5:76102262-76102271

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:76111995-76112045	HNPCEpiC	eye:	n/a
2	chr5:76108191-76108241	SK-N-MC	brain:	n/a
3	chr5:76111995-76112045	HNPCEpiC	eye:	n/a
4	chr5:76108191-76108241	SK-N-MC	brain:	n/a
5	chr5:76117747-76117797	HCPEpiC	choroid plexus:	n/a
6	chr5:76114933-76114983	HRE	kidney:	n/a
7	chr5:76112996-76113046	GM12891	blood:	n/a
8	chr5:76114646-76114696	Caco-2	colon:	n/a
9	chr5:76108729-76108779	AoSMC	blood vessel:	n/a
10	chr5:76115868-76115918	Hela-S3	cervix:	n/a
11	chr5:76116088-76116138	HRCEpiC	kidney:	n/a
12	chr5:76114646-76114696	MCF10A-Er-Src	breast:	n/a
13	chr5:76114822-76114872	K562	blood:	n/a
14	chr5:76114571-76114621	Hepatocyte	liver:	n/a
15	chr5:76116535-76116585	HEK293	kidney:	embryo
16	chr5:76108729-76108779	BJ	skin:	n/a
17	chr5:76114635-76114685	HRE	kidney:	n/a
18	chr5:76115309-76115359	GM12878	blood:	n/a
19	chr5:76114373-76114423	IMR90	lung:	fetal
20	chr5:76116169-76116219	H1-hESC	embryonic stem cell:	embryo
21	chr5:76114646-76114696	NT2-D1	testis:	n/a
22	chr5:76114571-76114621	MCF-7	breast:	n/a
23	chr5:76119931-76119981	HRPEpiC	eye:	n/a
24	chr5:76114933-76114983	AG04449	skin:	fetal
25	chr5:76114684-76114734	AG09319	gingival:	n/a
26	chr5:76115974-76116024	AG09319	gingival:	n/a
27	chr5:76115974-76116024	AG09309	skin:	n/a
28	chr5:76114373-76114423	H1-hESC	embryonic stem cell:	embryo
29	chr5:76116169-76116219	HRCEpiC	kidney:	n/a
30	chr5:76115868-76115918	ProgFib	skin:	n/a
31	chr5:76115810-76115860	NB4	blood:	n/a
32	chr5:76112996-76113046	HCPEpiC	choroid plexus:	n/a
33	chr5:76114822-76114872	SKMC	muscle:	n/a
34	chr5:76115810-76115860	HAEpiC	amniotic membrane:	n/a
35	chr5:76114522-76114572	AG09309	skin:	n/a
36	chr5:76114684-76114734	HCPEpiC	choroid plexus:	n/a
37	chr5:76116088-76116138	HCPEpiC	choroid plexus:	n/a
38	chr5:76116169-76116219	BE2_C	brain:	n/a
39	chr5:76117747-76117797	HMEC	breast:	n/a
40	chr5:76112996-76113046	GM06990	blood:	n/a
41	chr5:76114522-76114572	GM12878	blood:	n/a
42	chr5:76114571-76114621	HMEC	breast:	n/a
43	chr5:76114522-76114572	GM12891	blood:	n/a
44	chr5:76112776-76112826	SKMC	muscle:	n/a
45	chr5:76114812-76114862	NH-A	brain:	n/a
46	chr5:76112776-76112826	AG10803	skin:	n/a
47	chr5:76108729-76108779	K562	blood:	n/a
48	chr5:76114812-76114862	Caco-2	colon:	n/a
49	chr5:76114635-76114685	AG04450	lung:	fetal
50	chr5:76116088-76116138	HEK293	kidney:	embryo

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:76113078..76116046-chr5:76145704..76148210,2	K562	blood:
2	chr5:76123012..76125302-chr5:76125595..76128318,2	MCF-7	breast:
3	chr19:796813..797729-chr5:76114268..76115162,3	HCT-116	colon:
4	chr5:76094082..76095930-chr5:76098926..76101541,2	K562	blood:
5	chr5:76115175..76117196-chr5:76160540..76162682,2	MCF-7	breast:
6	chr5:76103612..76107653-chr5:76108707..76113004,3	MCF-7	breast:
7	chr5:76083391..76086055-chr5:76095285..76096948,2	MCF-7	breast:
8	chr5:76094082..76095930-chr5:76098926..76101541,2	K562	blood:
9	chr5:76094721..76097053-chr5:76101788..76104241,2	K562	blood:
10	chr5:76101619..76103504-chr5:76111998..76114759,2	K562	blood:
11	chr5:76083391..76086055-chr5:76095285..76096948,2	MCF-7	breast:
12	chr5:76103612..76107653-chr5:76108707..76113004,3	MCF-7	breast:
13	chr5:76110973..76114089-chr5:76116480..76119427,3	K562	blood:
14	chr5:76106690..76108652-chr5:76112389..76115245,2	K562	blood:
15	chr5:76123012..76125302-chr5:76125595..76128318,2	MCF-7	breast:
16	chr5:76127088..76128697-chr5:76136604..76139100,2	K562	blood:
17	chr5:76105222..76108652-chr5:76112389..76115245,3	K562	blood:
18	chr5:76094721..76097053-chr5:76101788..76104241,2	K562	blood:
19	chr5:76110973..76114089-chr5:76116480..76119427,3	K562	blood:
20	chr5:76115218..76117725-chr5:76325993..76327834,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-S100Z-1	chr5:76114806-76115096	NONHSAT102251

No data

Variant related genes	Relation type
ENSG00000238688	TF binding region
F2RL1	TF binding region
ENSG00000238688	CpG island
F2RL1	CpG island
ENSG00000164252	chromatin interactions
ENSG00000011304	chromatin interactions
ENSG00000171643	chromatin interactions
ENSG00000164251	chromatin interactions

Extended variants
information (count: 2087 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2087 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142665373	chr5:76079733-76079734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs114148399	chr5:76079738-76079739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368291719	chr5:76079785-76079786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573529863	chr5:76079789-76079790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552099014	chr5:76079823-76079824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558192075	chr5:76079845-76079846	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575581988	chr5:76079868-76079869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189891429	chr5:76079872-76079873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561092022	chr5:76079905-76079906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529042431	chr5:76079919-76079920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548724297	chr5:76079920-76079921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182517234	chr5:76079965-76079966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528338533	chr5:76080024-76080025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551423302	chr5:76080028-76080029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187259218	chr5:76080056-76080057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs193043281	chr5:76080134-76080135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369263932	chr5:76080149-76080150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550641871	chr5:76080160-76080161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185307450	chr5:76080205-76080206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146356352	chr5:76080271-76080272	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371814452	chr5:76080273-76080274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572010417	chr5:76080274-76080275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374739242	chr5:76080375-76080376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188973906	chr5:76080393-76080394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs367727330	chr5:76080396-76080397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs193150354	chr5:76080442-76080443	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139067653	chr5:76080453-76080454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555461375	chr5:76080465-76080466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs75712459	chr5:76080515-76080516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149373091	chr5:76080556-76080557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554548108	chr5:76080564-76080565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111685562	chr5:76080576-76080577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574566874	chr5:76080602-76080603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368775103	chr5:76080614-76080615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184737990	chr5:76080637-76080638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144741313	chr5:76080643-76080644	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528303489	chr5:76080743-76080744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544193535	chr5:76080778-76080779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545285138	chr5:76080782-76080783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565074210	chr5:76080827-76080828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs112359311	chr5:76080907-76080908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530845426	chr5:76080929-76080930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550259497	chr5:76080960-76080961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187959786	chr5:76080975-76080976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs373492157	chr5:76081009-76081010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs148026566	chr5:76081026-76081027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs180925145	chr5:76081030-76081031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs183854954	chr5:76081048-76081049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs399510	chr5:76081078-76081079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs28493768	chr5:76081093-76081094	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:87)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1626 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:76070600-76080600	Weak transcription	Fetal Intestine Small	intestine
2	chr5:76075400-76079800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr5:76075400-76080200	Weak transcription	Fetal Muscle Leg	muscle
4	chr5:76075600-76084200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr5:76075800-76079800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr5:76076000-76079800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr5:76076000-76083000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr5:76076000-76084200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr5:76077200-76081800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr5:76077600-76081400	Enhancers	A549	lung
11	chr5:76077800-76081600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr5:76077800-76085800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr5:76078200-76084200	Enhancers	HUVEC	blood vessel
14	chr5:76078800-76080200	Weak transcription	Fetal Intestine Large	intestine
15	chr5:76078800-76080600	Weak transcription	HepG2	liver
16	chr5:76078800-76081000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr5:76079000-76082800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr5:76079000-76083400	Weak transcription	Spleen	Spleen
19	chr5:76079000-76084200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr5:76079200-76080800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr5:76079400-76079800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr5:76079600-76079800	Enhancers	Stomach Mucosa	stomach
23	chr5:76079600-76080400	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr5:76079600-76080800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr5:76079800-76080400	Enhancers	H9 Cell Line	embryonic stem cell
26	chr5:76079800-76080400	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr5:76079800-76080600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr5:76079800-76081600	Weak transcription	Stomach Mucosa	stomach
29	chr5:76079800-76083000	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr5:76079800-76084000	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr5:76080000-76080600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr5:76080200-76080600	Enhancers	Fetal Muscle Leg	muscle
33	chr5:76080200-76084600	Enhancers	Fetal Intestine Large	intestine
34	chr5:76080400-76080800	Enhancers	Small Intestine	intestine
35	chr5:76080400-76082800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr5:76080400-76086800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr5:76080600-76080800	Enhancers	Colonic Mucosa	Colon
38	chr5:76080600-76081800	Enhancers	HepG2	liver
39	chr5:76080600-76082000	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr5:76080600-76082200	Enhancers	Fetal Intestine Small	intestine
41	chr5:76080600-76082800	Weak transcription	Fetal Muscle Leg	muscle
42	chr5:76080600-76083000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr5:76080600-76086800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr5:76080800-76081200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr5:76080800-76081200	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr5:76080800-76085800	Weak transcription	Small Intestine	intestine
47	chr5:76080800-76086600	Weak transcription	Colonic Mucosa	Colon
48	chr5:76081000-76081600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr5:76081000-76082200	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr5:76081000-76082200	Enhancers	NH-A	brain

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