Variant report

Variant	nsv1022431
Chromosome Location	chr5:76086795-76127170
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1588)
CpG islands
(count:1529)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:76113989-76114292	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:76101782-76102245	K562	blood:	n/a	n/a
3	ARID3A	chr5:76114553-76114860	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:76086428-76087095	K562	blood:	n/a	n/a
5	ARID3A	chr5:76126576-76126776	K562	blood:	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	ATF1	chr5:76101722-76102174	K562	blood:	n/a	n/a
9	ATF1	chr5:76086458-76087131	K562	blood:	n/a	n/a
10	ATF2	chr5:76114079-76115052	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr5:76086364-76086842	GM12878	blood:	n/a	n/a
12	ATF2	chr5:76113947-76114568	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr5:76126950-76127363	GM12878	blood:	n/a	n/a
14	ATF2	chr5:76126912-76127331	GM12878	blood:	n/a	n/a
15	ATF2	chr5:76103823-76104436	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr5:76103843-76104561	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr5:76099975-76100655	A549	lung:	n/a	n/a
18	ATF3	chr5:76100044-76100672	A549	lung:	n/a	n/a
19	ATF3	chr5:76086335-76086970	A549	lung:	n/a	n/a
20	ATF3	chr5:76114432-76115010	A549	lung:	n/a	chr5:76114977-76114986 chr5:76114862-76114870
21	ATF3	chr5:76086333-76087061	A549	lung:	n/a	n/a
22	ATF3	chr5:76101689-76102467	A549	lung:	n/a	n/a
23	ATF3	chr5:76086822-76087094	K562	blood:	n/a	n/a
24	ATF3	chr5:76114447-76115003	A549	lung:	n/a	chr5:76114977-76114986 chr5:76114862-76114870
25	ATF3	chr5:76101627-76102562	A549	lung:	n/a	n/a
26	BACH1	chr5:76103704-76103712	K562	blood:	n/a	n/a
27	BACH1	chr5:76114200-76116153	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr5:76126596-76126774	K562	blood:	n/a	n/a
29	BATF	chr5:76102000-76102358	GM12878	blood:	n/a	n/a
30	BATF	chr5:76126956-76127325	GM12878	blood:	n/a	n/a
31	BATF	chr5:76086446-76086954	GM12878	blood:	n/a	chr5:76086559-76086569
32	BCL11A	chr5:76126997-76127227	GM12878	blood:	n/a	chr5:76127105-76127114
33	BCL11A	chr5:76086438-76086837	GM12878	blood:	n/a	n/a
34	BCL11A	chr5:76126931-76127279	GM12878	blood:	n/a	chr5:76127105-76127114
35	BCL3	chr5:76101399-76102582	A549	lung:	n/a	chr5:76102262-76102271
36	BCL3	chr5:76126569-76127455	A549	lung:	n/a	chr5:76127105-76127114
37	BCL3	chr5:76099724-76100840	A549	lung:	n/a	chr5:76100092-76100100 chr5:76100201-76100210
38	BCL3	chr5:76126926-76127294	GM12878	blood:	n/a	chr5:76127105-76127114
39	BCL3	chr5:76086154-76087174	A549	lung:	n/a	n/a
40	BCL3	chr5:76101972-76102349	GM12878	blood:	n/a	chr5:76102262-76102271
41	BCL3	chr5:76101997-76102356	GM12878	blood:	n/a	chr5:76102262-76102271
42	BCL3	chr5:76126827-76127402	A549	lung:	n/a	chr5:76127105-76127114
43	BCL3	chr5:76086213-76087155	A549	lung:	n/a	n/a
44	BCL3	chr5:76097061-76097862	A549	lung:	n/a	n/a
45	BCL3	chr5:76101545-76102516	A549	lung:	n/a	chr5:76102262-76102271
46	BCL3	chr5:76115978-76116822	A549	lung:	n/a	n/a
47	BCL3	chr5:76099974-76100817	A549	lung:	n/a	chr5:76100092-76100100 chr5:76100201-76100210
48	BCL3	chr5:76126983-76127322	GM12878	blood:	n/a	chr5:76127105-76127114
49	BCL3	chr5:76114082-76115135	A549	lung:	n/a	chr5:76114962-76114971 chr5:76114691-76114704
50	BCL3	chr5:76109782-76110506	A549	lung:	n/a	chr5:76110348-76110357

(count:1529 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:76115868-76115918	GM12891	blood:	n/a
2	chr5:76112996-76113046	GM19239	blood:	n/a
3	chr5:76114812-76114862	Hepatocyte	liver:	n/a
4	chr5:76108191-76108241	HepG2	liver:	n/a
5	chr5:76115868-76115918	GM12891	blood:	n/a
6	chr5:76112996-76113046	GM19239	blood:	n/a
7	chr5:76114812-76114862	Hepatocyte	liver:	n/a
8	chr5:76108191-76108241	HepG2	liver:	n/a
9	chr5:76115974-76116024	SK-N-SH_RA	brain:	n/a
10	chr5:76114571-76114621	SK-N-SH_RA	brain:	n/a
11	chr5:76114812-76114862	Caco-2	colon:	n/a
12	chr5:76114933-76114983	AG10803	skin:	n/a
13	chr5:76115672-76115722	SAEC	small airway:	n/a
14	chr5:76114646-76114696	ECC-1	luminal epithelium:	n/a
15	chr5:76087172-76087222	HPAEpiC	pulmonary alveolar:	n/a
16	chr5:76114933-76114983	SK-N-MC	brain:	n/a
17	chr5:76114812-76114862	NB4	blood:	n/a
18	chr5:76117747-76117797	MCF10A-Er-Src	breast:	n/a
19	chr5:76115974-76116024	Hepatocyte	liver:	n/a
20	chr5:76114571-76114621	Caco-2	colon:	n/a
21	chr5:76108191-76108241	T-47D	breast:	n/a
22	chr5:76116535-76116585	NB4	blood:	n/a
23	chr5:76114812-76114862	HCF	heart:	n/a
24	chr5:76115810-76115860	NB4	blood:	n/a
25	chr5:76115810-76115860	NHBE	bronchial:	n/a
26	chr5:76108729-76108779	BJ	skin:	n/a
27	chr5:76114812-76114862	AG09309	skin:	n/a
28	chr5:76112776-76112826	HL-60	blood:	n/a
29	chr5:76112776-76112826	AG04449	skin:	fetal
30	chr5:76115672-76115722	GM12878	blood:	n/a
31	chr5:76115974-76116024	H1-hESC	embryonic stem cell:	embryo
32	chr5:76116169-76116219	HEEpiC	esophagus:	n/a
33	chr5:76114684-76114734	HRPEpiC	eye:	n/a
34	chr5:76116535-76116585	ECC-1	luminal epithelium:	n/a
35	chr5:76115672-76115722	BE2_C	brain:	n/a
36	chr5:76111995-76112045	MCF-7	breast:	n/a
37	chr5:76114635-76114685	NHBE	bronchial:	n/a
38	chr5:76112776-76112826	ovcar-3	ovarian:	n/a
39	chr5:76116088-76116138	Hela-S3	cervix:	n/a
40	chr5:76087172-76087222	SAEC	small airway:	n/a
41	chr5:76117747-76117797	Caco-2	colon:	n/a
42	chr5:76114933-76114983	HEEpiC	esophagus:	n/a
43	chr5:76114684-76114734	NHDF-neo	bronchial:	n/a
44	chr5:76116535-76116585	HAEpiC	amniotic membrane:	n/a
45	chr5:76108191-76108241	Caco-2	colon:	n/a
46	chr5:76115868-76115918	AG09309	skin:	n/a
47	chr5:76114933-76114983	GM06990	blood:	n/a
48	chr5:76112776-76112826	HRCEpiC	kidney:	n/a
49	chr5:76112996-76113046	NH-A	brain:	n/a
50	chr5:76116535-76116585	HNPCEpiC	eye:	n/a

(count:19 , 50 per page) page: 1

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

(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
F2RL1	TF binding region
F2RL1	CpG island
ENSG00000011304	chromatin interactions
ENSG00000171643	chromatin interactions
ENSG00000164252	chromatin interactions
ENSG00000164251	chromatin interactions

Extended variants
information (count: 1676 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1676 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17682153	chr5:76086795-76086796	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs564854615	chr5:76086853-76086854	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs530570574	chr5:76086922-76086923	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs550685010	chr5:76086927-76086928	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs530286925	chr5:76087012-76087013	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs16873772	chr5:76087127-76087128	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs80062652	chr5:76087180-76087181	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs546848960	chr5:76087190-76087191	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs184643326	chr5:76087212-76087213	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs375237340	chr5:76087224-76087225	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs538948874	chr5:76087303-76087304	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs112811064	chr5:76087353-76087354	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs189920303	chr5:76087371-76087372	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs375781804	chr5:76087438-76087439	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs73131652	chr5:76087440-76087441	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs114379267	chr5:76087585-76087586	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs574564789	chr5:76087587-76087588	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs534316418	chr5:76087612-76087613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552878547	chr5:76087694-76087695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532593864	chr5:76087710-76087711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs58911776	chr5:76087818-76087819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148918224	chr5:76087850-76087851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565220298	chr5:76087884-76087885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs192105480	chr5:76087907-76087908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115902198	chr5:76087965-76087966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs143650399	chr5:76087974-76087975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs151048539	chr5:76088020-76088021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546708684	chr5:76088041-76088042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537158419	chr5:76088043-76088044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs73131653	chr5:76088067-76088068	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs566768774	chr5:76088068-76088069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532786805	chr5:76088074-76088075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552442926	chr5:76088106-76088107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs569161694	chr5:76088143-76088144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs116256911	chr5:76088218-76088219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs548144600	chr5:76088248-76088249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184645904	chr5:76088346-76088347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528122194	chr5:76088449-76088450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs397998210	chr5:76088469-76088470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189456324	chr5:76088515-76088516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554290771	chr5:76088521-76088522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182057876	chr5:76088522-76088523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs187432139	chr5:76088538-76088539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs138649902	chr5:76088545-76088546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567276131	chr5:76088546-76088547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575579470	chr5:76088551-76088552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189054680	chr5:76088598-76088599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs376162065	chr5:76088614-76088615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs180967450	chr5:76088619-76088620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571466822	chr5:76088627-76088628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

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:1301 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:76080400-76086800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr5:76080600-76086800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr5:76081600-76088800	Enhancers	Stomach Mucosa	stomach
4	chr5:76083000-76087800	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr5:76083400-76089200	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr5:76084000-76088200	Enhancers	Fetal Lung	lung
7	chr5:76084200-76088200	Enhancers	Fetal Stomach	stomach
8	chr5:76084200-76088400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr5:76084400-76086800	Weak transcription	Pancreas	Pancrea
10	chr5:76084600-76087400	Weak transcription	Liver	Liver
11	chr5:76085200-76087600	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr5:76085200-76088000	Enhancers	NHLF	lung
13	chr5:76085400-76087800	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr5:76085400-76088000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr5:76085400-76088000	Enhancers	Adipose Nuclei	Adipose
16	chr5:76085400-76088000	Enhancers	Spleen	Spleen
17	chr5:76085400-76088200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr5:76085400-76088200	Enhancers	HMEC	breast
19	chr5:76085600-76087200	Flanking Active TSS	A549	lung
20	chr5:76085600-76087800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr5:76085600-76088000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr5:76085600-76088000	Enhancers	Brain Hippocampus Middle	brain
23	chr5:76085600-76088200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr5:76085600-76088200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr5:76085600-76088400	Enhancers	Fetal Muscle Leg	muscle
26	chr5:76085600-76090400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr5:76085800-76086800	Enhancers	Placenta	Placenta
28	chr5:76085800-76086800	Enhancers	HSMM	muscle
29	chr5:76085800-76087000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr5:76085800-76087000	Flanking Active TSS	NHEK	skin
31	chr5:76085800-76087200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr5:76085800-76087200	Enhancers	Esophagus	oesophagus
33	chr5:76085800-76087200	Enhancers	Right Atrium	heart
34	chr5:76085800-76087200	Enhancers	K562	blood
35	chr5:76085800-76087800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr5:76085800-76087800	Enhancers	Fetal Intestine Small	intestine
37	chr5:76085800-76087800	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr5:76085800-76087800	Enhancers	Small Intestine	intestine
39	chr5:76085800-76088000	Enhancers	Duodenum Mucosa	Duodenum
40	chr5:76085800-76088200	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr5:76085800-76088800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr5:76086000-76086800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr5:76086000-76086800	Weak transcription	Gastric	stomach
44	chr5:76086000-76087000	Weak transcription	Left Ventricle	heart
45	chr5:76086000-76087000	Enhancers	NH-A	brain
46	chr5:76086000-76087200	Enhancers	Primary T cells fromperipheralblood	blood
47	chr5:76086000-76087400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr5:76086000-76087400	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr5:76086000-76087600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr5:76086000-76087600	Enhancers	Primary T helper cells PMA-I stimulated	--

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