Variant report

Variant	nsv1018078
Chromosome Location	chr5:112615220-112657404
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:510)
CpG islands
(count:1223)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:510 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:112628719-112629245	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr5:112628825-112629240	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr5:112629022-112630707	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr5:112653498-112653533	K562	blood:	n/a	n/a
5	CEBPB	chr5:112616373-112616608	HepG2	liver:	n/a	chr5:112616438-112616449
6	CEBPB	chr5:112630638-112630704	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr5:112655415-112655423	K562	blood:	n/a	n/a
8	CEBPB	chr5:112647167-112647457	Hela-S3	cervix:	n/a	chr5:112647355-112647366 chr5:112647355-112647368 chr5:112647355-112647368
9	CEBPB	chr5:112647304-112647387	K562	blood:	n/a	chr5:112647355-112647366 chr5:112647355-112647368 chr5:112647355-112647368
10	CEBPB	chr5:112616294-112616612	IMR90	lung:	n/a	chr5:112616438-112616449
11	CEBPB	chr5:112624979-112625014	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr5:112647248-112647479	HepG2	liver:	n/a	chr5:112647355-112647366 chr5:112647355-112647368 chr5:112647355-112647368
13	CEBPB	chr5:112647241-112647408	A549	lung:	n/a	chr5:112647355-112647366 chr5:112647355-112647368 chr5:112647355-112647368
14	CEBPB	chr5:112648586-112648930	Hela-S3	cervix:	n/a	n/a
15	CEBPD	chr5:112616859-112617279	K562	blood:	n/a	n/a
16	CHD1	chr5:112629583-112630989	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTBP2	chr5:112629912-112630843	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTBP2	chr5:112628579-112629678	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr5:112630460-112630610	HBMEC	blood vessel:	n/a	n/a
20	CTCF	chr5:112630940-112631090	HAc	cerebellar:	n/a	n/a
21	CTCF	chr5:112631000-112631150	HA-sp	spinal cord:	n/a	n/a
22	CTCF	chr5:112657080-112657230	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr5:112657060-112657210	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr5:112630480-112630630	NHDF-neo	bronchial:	n/a	n/a
25	CTCF	chr5:112630440-112630590	RPTEC	kidney:	n/a	n/a
26	CTCF	chr5:112630980-112631130	AG04449	skin:	n/a	n/a
27	CTCF	chr5:112631040-112631190	AG10803	skin:	n/a	n/a
28	CTCF	chr5:112630997-112631146	MCF-7	breast:	n/a	n/a
29	CTCF	chr5:112623560-112623710	HepG2	liver:	n/a	n/a
30	CTCF	chr5:112630370-112630656	GM19238	blood:	n/a	n/a
31	CTCF	chr5:112630540-112630690	BE2_C	brain:	n/a	n/a
32	CTCF	chr5:112631000-112631150	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr5:112630525-112630532	Pancreas_OC	pancreas:	n/a	n/a
34	CTCF	chr5:112630399-112630591	LNCaP	prostate:	n/a	n/a
35	CTCF	chr5:112631020-112631170	RPTEC	kidney:	n/a	n/a
36	CTCF	chr5:112631020-112631170	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr5:112630360-112630510	GM12878	blood:	n/a	n/a
38	CTCF	chr5:112630440-112630590	GM06990	blood:	n/a	n/a
39	CTCF	chr5:112630960-112631110	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr5:112631020-112631170	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr5:112630460-112630610	NHEK	skin:	n/a	n/a
42	CTCF	chr5:112630920-112631070	HCT-116	colon:	n/a	n/a
43	CTCF	chr5:112630543-112630619	Pancreas_OC	pancreas:	n/a	n/a
44	CTCF	chr5:112630420-112630570	GM12867	blood:	n/a	n/a
45	CTCF	chr5:112630381-112630663	MCF-7	breast:	n/a	n/a
46	CTCF	chr5:112630540-112630690	HPF	lung:	n/a	n/a
47	CTCF	chr5:112630254-112630338	MCF-7	breast:	n/a	n/a
48	CTCF	chr5:112630500-112630650	BJ	skin:	n/a	n/a
49	CTCF	chr5:112657100-112657250	BE2_C	brain:	n/a	n/a
50	CTCF	chr5:112630410-112630617	GM12891	blood:	n/a	n/a

(count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:112630990-112631040	GM12892	blood:	n/a
2	chr5:112630684-112630734	SK-N-SH_RA	brain:	n/a
3	chr5:112634436-112634486	HCF	heart:	n/a
4	chr5:112630990-112631040	GM12892	blood:	n/a
5	chr5:112630684-112630734	SK-N-SH_RA	brain:	n/a
6	chr5:112634436-112634486	HCF	heart:	n/a
7	chr5:112615762-112615812	NB4	blood:	n/a
8	chr5:112631052-112631102	HNPCEpiC	eye:	n/a
9	chr5:112629604-112629654	AG09309	skin:	n/a
10	chr5:112630684-112630734	HRE	kidney:	n/a
11	chr5:112622133-112622183	HRE	kidney:	n/a
12	chr5:112630684-112630734	AG09309	skin:	n/a
13	chr5:112630684-112630734	Caco-2	colon:	n/a
14	chr5:112630811-112630861	HCPEpiC	choroid plexus:	n/a
15	chr5:112630695-112630745	AG09309	skin:	n/a
16	chr5:112615762-112615812	K562	blood:	n/a
17	chr5:112630413-112630463	SK-N-SH_RA	brain:	n/a
18	chr5:112630990-112631040	HUVEC	blood vessel:	n/a
19	chr5:112655559-112655609	HPAEpiC	pulmonary alveolar:	n/a
20	chr5:112634436-112634486	HepG2	liver:	n/a
21	chr5:112630811-112630861	NT2-D1	testis:	n/a
22	chr5:112630413-112630463	SAEC	small airway:	n/a
23	chr5:112629565-112629615	Jurkat	blood:	n/a
24	chr5:112629565-112629615	ECC-1	luminal epithelium:	n/a
25	chr5:112627446-112627496	PFSK-1	brain:	n/a
26	chr5:112629565-112629615	K562	blood:	n/a
27	chr5:112630695-112630745	PANC-1	pancreas:	n/a
28	chr5:112631526-112631576	NH-A	brain:	n/a
29	chr5:112630695-112630745	HRE	kidney:	n/a
30	chr5:112630041-112630091	K562	blood:	n/a
31	chr5:112630990-112631040	U87	brain:	n/a
32	chr5:112627446-112627496	HUVEC	blood vessel:	n/a
33	chr5:112630225-112630275	NH-A	brain:	n/a
34	chr5:112629565-112629615	Hepatocyte	liver:	n/a
35	chr5:112630811-112630861	SKMC	muscle:	n/a
36	chr5:112629604-112629654	NT2-D1	testis:	n/a
37	chr5:112629565-112629615	HUVEC	blood vessel:	n/a
38	chr5:112630041-112630091	BE2_C	brain:	n/a
39	chr5:112630041-112630091	GM19239	blood:	n/a
40	chr5:112630041-112630091	GM12878	blood:	n/a
41	chr5:112630811-112630861	GM06990	blood:	n/a
42	chr5:112630623-112630673	HRCEpiC	kidney:	n/a
43	chr5:112631052-112631102	HCT-116	colon:	n/a
44	chr5:112630684-112630734	SKMC	muscle:	n/a
45	chr5:112629604-112629654	HEK293	kidney:	embryo
46	chr5:112615762-112615812	HRE	kidney:	n/a
47	chr5:112630225-112630275	HCF	heart:	n/a
48	chr5:112631526-112631576	BJ	skin:	n/a
49	chr5:112629565-112629615	PFSK-1	brain:	n/a
50	chr5:112630225-112630275	AG04450	lung:	fetal

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:112616654..112618757-chr5:112626610..112628435,2	MCF-7	breast:
2	chr5:112637840..112639791-chr5:112646688..112648404,2	MCF-7	breast:
3	chr14:51874487..51876257-chr5:112637673..112640166,2	MCF-7	breast:
4	chr5:112628459..112631026-chr5:112632248..112634333,2	MCF-7	breast:
5	chr5:112608585..112610553-chr5:112626855..112628809,2	MCF-7	breast:
6	chr5:112621858..112623508-chr5:112628584..112630784,2	K562	blood:
7	chr5:112619318..112622139-chr5:112627969..112630686,2	MCF-7	breast:
8	chr5:112616654..112618757-chr5:112626610..112628435,2	MCF-7	breast:
9	chr4:32159312..32160248-chr5:112648833..112649616,2	K562	blood:
10	chr5:112628328..112630254-chr5:112656025..112657722,2	MCF-7	breast:
11	chr5:112628328..112630254-chr5:112656025..112657722,2	MCF-7	breast:
12	chr5:112637840..112639791-chr5:112646688..112648404,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000232633	TF binding region
MCC	TF binding region
ENSG00000232633	CpG island
MCC	CpG island
ENSG00000171444	chromatin interactions

Extended variants
information (count: 1643 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1643 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369930170	chr5:112615230-112615231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs114711351	chr5:112615235-112615236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs188931530	chr5:112615237-112615238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181379628	chr5:112615251-112615252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs564763476	chr5:112615259-112615260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528768121	chr5:112615260-112615261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547216884	chr5:112615272-112615273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142012398	chr5:112615275-112615276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535576596	chr5:112615290-112615291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575147060	chr5:112615354-112615355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550660578	chr5:112615359-112615360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs13190161	chr5:112615386-112615387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116199313	chr5:112615395-112615396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs77843857	chr5:112615417-112615418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185513368	chr5:112615439-112615440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533824284	chr5:112615454-112615455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs530590726	chr5:112615496-112615497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150680280	chr5:112615516-112615517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs118007208	chr5:112615558-112615559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369859223	chr5:112615560-112615561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541943241	chr5:112615579-112615580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs17135542	chr5:112615626-112615627	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs116483079	chr5:112615700-112615701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546222214	chr5:112615719-112615720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs558938373	chr5:112615728-112615729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs17135543	chr5:112615745-112615746	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs531850200	chr5:112615763-112615764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs549825104	chr5:112615769-112615770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546959778	chr5:112615822-112615823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562321676	chr5:112615827-112615828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs377580997	chr5:112615828-112615829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550697652	chr5:112615838-112615839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191292560	chr5:112615860-112615861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539536766	chr5:112615878-112615879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551384912	chr5:112615883-112615884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566329205	chr5:112615885-112615886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs370476474	chr5:112615904-112615905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534107930	chr5:112615912-112615913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs180954723	chr5:112615943-112615944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs573502245	chr5:112615950-112615951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185997722	chr5:112615959-112615960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs555927988	chr5:112615975-112615976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs116166246	chr5:112615986-112615987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192095717	chr5:112615987-112615988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564541835	chr5:112615992-112615993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139486200	chr5:112615998-112615999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149663421	chr5:112616009-112616010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147702788	chr5:112616018-112616019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146583585	chr5:112616026-112616027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs73246648	chr5:112616124-112616125	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

Disease	PMID	Source
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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Colorectal cancer	21297112	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Sezary syndrome	18413736	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1019 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:112586600-112623600	Weak transcription	Pancreas	Pancrea
2	chr5:112587600-112617000	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr5:112600200-112618000	Weak transcription	Fetal Kidney	kidney
4	chr5:112602200-112616600	Weak transcription	Brain Hippocampus Middle	brain
5	chr5:112603000-112616800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr5:112607600-112616200	Weak transcription	Esophagus	oesophagus
7	chr5:112608000-112628200	Weak transcription	HMEC	breast
8	chr5:112610000-112628200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr5:112610800-112616400	Weak transcription	Spleen	Spleen
10	chr5:112610800-112623200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr5:112611000-112616600	Weak transcription	Psoas Muscle	Psoas
12	chr5:112611000-112618000	Weak transcription	Fetal Stomach	stomach
13	chr5:112611000-112628200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr5:112611200-112618000	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr5:112611400-112616400	Weak transcription	Adipose Nuclei	Adipose
16	chr5:112611400-112616400	Weak transcription	HUVEC	blood vessel
17	chr5:112612000-112616400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr5:112612000-112616600	Weak transcription	Stomach Smooth Muscle	stomach
19	chr5:112612000-112618000	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr5:112612000-112623800	Weak transcription	Fetal Muscle Leg	muscle
21	chr5:112612000-112625200	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr5:112612200-112616400	Weak transcription	Liver	Liver
23	chr5:112612200-112616800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr5:112612200-112616800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr5:112612200-112617000	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr5:112612200-112625200	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr5:112612400-112615400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr5:112612400-112616400	Weak transcription	Brain Cingulate Gyrus	brain
29	chr5:112612400-112617000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr5:112612400-112617000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr5:112612400-112618400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr5:112612600-112616400	Weak transcription	Brain Substantia Nigra	brain
33	chr5:112612600-112617200	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr5:112613400-112618000	Enhancers	Ovary	ovary
35	chr5:112613600-112617200	Enhancers	Left Ventricle	heart
36	chr5:112614200-112615400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr5:112614200-112617000	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr5:112614200-112625200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr5:112614400-112615400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr5:112614400-112616400	Weak transcription	Lung	lung
41	chr5:112614400-112616600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr5:112614400-112617000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
43	chr5:112614400-112617400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr5:112614600-112615800	Weak transcription	Right Ventricle	heart
45	chr5:112615000-112615400	Weak transcription	Fetal Heart	heart
46	chr5:112615000-112616400	Weak transcription	NH-A	brain
47	chr5:112615000-112617200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr5:112615000-112625200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr5:112615200-112615600	Weak transcription	Right Atrium	heart
50	chr5:112615200-112616000	Enhancers	HUES48 Cell Line	embryonic stem cell

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