Variant report

Variant	nsv10703
Chromosome Location	chr5:61596178-61601493
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	chr5:61601469-61601973	K562	blood:	n/a	n/a
2	ATF2	chr5:61601195-61601869	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr5:61601492-61602007	GM12878	blood:	n/a	n/a
4	ATF2	chr5:61601440-61601953	GM12878	blood:	n/a	n/a
5	BCL3	chr5:61601415-61601940	A549	lung:	n/a	chr5:61601867-61601880 chr5:61601883-61601896 chr5:61601868-61601881
6	BCLAF1	chr5:61601428-61602051	GM12878	blood:	n/a	chr5:61601867-61601880 chr5:61602011-61602024 chr5:61601883-61601896 chr5:61601868-61601881
7	BCLAF1	chr5:61601477-61602220	GM12878	blood:	n/a	chr5:61601867-61601880 chr5:61602011-61602024 chr5:61601883-61601896 chr5:61601868-61601881
8	BHLHE40	chr5:61601099-61602473	K562	blood:	n/a	chr5:61602007-61602023 chr5:61601867-61601883 chr5:61601877-61601893
9	BRCA1	chr5:61601412-61601789	H1-hESC	embryonic stem cell:	n/a	n/a
10	CBX3	chr5:61600931-61602228	K562	blood:	n/a	n/a
11	CBX3	chr5:61601212-61601893	K562	blood:	n/a	n/a
12	CHD1	chr5:61601425-61602126	GM12878	blood:	n/a	n/a
13	CHD2	chr5:61601377-61601879	HepG2	liver:	n/a	n/a
14	CHD2	chr5:61601096-61603020	K562	blood:	n/a	n/a
15	CHD2	chr5:61601480-61603312	GM12878	blood:	n/a	n/a
16	CHD2	chr5:61601394-61601927	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr5:61601313-61602592	K562	blood:	n/a	n/a
18	CREB1	chr5:61601437-61602558	K562	blood:	n/a	n/a
19	CREB1	chr5:61601441-61602577	A549	lung:	n/a	n/a
20	CREB1	chr5:61601452-61603144	HepG2	liver:	n/a	n/a
21	CREB1	chr5:61601389-61603298	GM12878	blood:	n/a	n/a
22	CREB1	chr5:61601468-61602064	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr5:61601407-61602132	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTBP2	chr5:61601277-61602139	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr5:61601443-61602070	H1-hESC	embryonic stem cell:	n/a	chr5:61601906-61601919 chr5:61602009-61602022 chr5:61601903-61601916
26	CTCF	chr5:61601460-61601610	MCF-7	breast:	n/a	n/a
27	CTCF	chr5:61601460-61601610	Caco-2	colon:	n/a	n/a
28	CTCF	chr5:61601264-61602093	K562	blood:	n/a	chr5:61601906-61601919 chr5:61602009-61602022 chr5:61601903-61601916
29	CTCF	chr5:61601466-61602292	GM12878	blood:	n/a	chr5:61601906-61601919 chr5:61602009-61602022 chr5:61601903-61601916 chr5:61602143-61602156
30	CTCF	chr5:61601057-61601109	Lung_OC	lung:	n/a	n/a
31	CTCF	chr5:61601440-61601590	GM12873	blood:	n/a	n/a
32	CTCF	chr5:61601400-61601550	HCPEpiC	choroid plexus:	n/a	n/a
33	E2F4	chr5:61601160-61602476	K562	blood:	n/a	chr5:61601985-61601994 chr5:61601770-61601781 chr5:61601969-61601978
34	E2F4	chr5:61601283-61602092	MCF10A-Er-Src	breast:	n/a	chr5:61601985-61601994 chr5:61601770-61601781 chr5:61601969-61601978
35	E2F4	chr5:61601359-61602116	Hela-S3	cervix:	n/a	chr5:61601985-61601994 chr5:61601770-61601781 chr5:61601969-61601978
36	E2F6	chr5:61601328-61603234	Hela-S3	cervix:	n/a	chr5:61602800-61602812 chr5:61601985-61601994 chr5:61602798-61602807 chr5:61601770-61601781 chr5:61601969-61601978
37	E2F6	chr5:61601363-61602012	A549	lung:	n/a	chr5:61601985-61601994 chr5:61601770-61601781 chr5:61601969-61601978
38	E2F6	chr5:61601349-61602129	K562	blood:	n/a	chr5:61601985-61601994 chr5:61601770-61601781 chr5:61601969-61601978
39	E2F6	chr5:61601464-61602202	K562	blood:	n/a	chr5:61601985-61601994 chr5:61601770-61601781 chr5:61601969-61601978
40	E2F6	chr5:61601182-61602199	A549	lung:	n/a	chr5:61601985-61601994 chr5:61601770-61601781 chr5:61601969-61601978
41	E2F6	chr5:61601387-61602229	H1-hESC	embryonic stem cell:	n/a	chr5:61601985-61601994 chr5:61601770-61601781 chr5:61601969-61601978
42	E2F6	chr5:61601013-61602183	H1-hESC	embryonic stem cell:	n/a	chr5:61601985-61601994 chr5:61601770-61601781 chr5:61601969-61601978
43	E2F6	chr5:61600954-61603294	K562	blood:	n/a	chr5:61602800-61602812 chr5:61601985-61601994 chr5:61602798-61602807 chr5:61601770-61601781 chr5:61601969-61601978
44	EBF1	chr5:61601163-61601974	GM12878	blood:	n/a	chr5:61601302-61601311 chr5:61601301-61601311
45	ELF1	chr5:61601358-61602106	K562	blood:	n/a	chr5:61601735-61601744 chr5:61601736-61601745 chr5:61601732-61601745 chr5:61601953-61601962 chr5:61601867-61601879
46	ELF1	chr5:61601442-61602603	K562	blood:	n/a	chr5:61602117-61602129 chr5:61601735-61601744 chr5:61602480-61602492 chr5:61601736-61601745 chr5:61601732-61601745 chr5:61601953-61601962 chr5:61601867-61601879
47	ELF1	chr5:61601460-61602212	GM12878	blood:	n/a	chr5:61602117-61602129 chr5:61601735-61601744 chr5:61601736-61601745 chr5:61601732-61601745 chr5:61601953-61601962 chr5:61601867-61601879
48	ELF1	chr5:61601427-61602109	SK-N-SH	brain:	n/a	chr5:61601735-61601744 chr5:61601736-61601745 chr5:61601732-61601745 chr5:61601953-61601962 chr5:61601867-61601879
49	ELF1	chr5:61601475-61602130	HepG2	liver:	n/a	chr5:61602117-61602129 chr5:61601735-61601744 chr5:61601736-61601745 chr5:61601732-61601745 chr5:61601953-61601962 chr5:61601867-61601879
50	ELF1	chr5:61601461-61602259	MCF-7	breast:	n/a	chr5:61602117-61602129 chr5:61601735-61601744 chr5:61601736-61601745 chr5:61601732-61601745 chr5:61601953-61601962 chr5:61601867-61601879

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:61598126-61598176	BJ	skin:	n/a
2	chr5:61598126-61598176	HAEpiC	amniotic membrane:	n/a
3	chr5:61601128-61601178	GM12878	blood:	n/a
4	chr5:61601128-61601178	HCM	heart:	n/a
5	chr5:61598126-61598176	HEK293	kidney:	embryo
6	chr5:61601128-61601178	AoSMC	blood vessel:	n/a
7	chr5:61601128-61601178	HCF	heart:	n/a
8	chr5:61598126-61598176	Jurkat	blood:	n/a
9	chr5:61601128-61601178	NHBE	bronchial:	n/a
10	chr5:61601128-61601178	HEEpiC	esophagus:	n/a
11	chr5:61601128-61601178	HUVEC	blood vessel:	n/a
12	chr5:61598126-61598176	U87	brain:	n/a
13	chr5:61601128-61601178	ECC-1	luminal epithelium:	n/a
14	chr5:61601128-61601178	HNPCEpiC	eye:	n/a
15	chr5:61601128-61601178	H1-hESC	embryonic stem cell:	embryo
16	chr5:61598126-61598176	NT2-D1	testis:	n/a
17	chr5:61601128-61601178	PFSK-1	brain:	n/a
18	chr5:61601128-61601178	K562	blood:	n/a
19	chr5:61598126-61598176	SAEC	small airway:	n/a
20	chr5:61598126-61598176	HCPEpiC	choroid plexus:	n/a
21	chr5:61601128-61601178	ProgFib	skin:	n/a
22	chr5:61598126-61598176	HEEpiC	esophagus:	n/a
23	chr5:61601128-61601178	Hela-S3	cervix:	n/a
24	chr5:61598126-61598176	AG04449	skin:	fetal
25	chr5:61598126-61598176	GM06990	blood:	n/a
26	chr5:61598126-61598176	NHBE	bronchial:	n/a
27	chr5:61598126-61598176	HPAEpiC	pulmonary alveolar:	n/a
28	chr5:61601128-61601178	AG09309	skin:	n/a
29	chr5:61601128-61601178	HIPEpiC	eye:	n/a
30	chr5:61601128-61601178	SAEC	small airway:	n/a
31	chr5:61601128-61601178	HCT-116	colon:	n/a
32	chr5:61598126-61598176	HepG2	liver:	n/a
33	chr5:61598126-61598176	H1-hESC	embryonic stem cell:	embryo
34	chr5:61598126-61598176	MCF-7	breast:	n/a
35	chr5:61601128-61601178	IMR90	lung:	fetal
36	chr5:61601128-61601178	HPAEpiC	pulmonary alveolar:	n/a
37	chr5:61601128-61601178	BE2_C	brain:	n/a
38	chr5:61601128-61601178	U87	brain:	n/a
39	chr5:61598126-61598176	HNPCEpiC	eye:	n/a
40	chr5:61598126-61598176	HCF	heart:	n/a
41	chr5:61598126-61598176	CMK	blood:	n/a
42	chr5:61598126-61598176	SKMC	muscle:	n/a
43	chr5:61598126-61598176	NHDF-neo	bronchial:	n/a
44	chr5:61598126-61598176	AG09309	skin:	n/a
45	chr5:61601128-61601178	GM12891	blood:	n/a
46	chr5:61598126-61598176	Caco-2	colon:	n/a
47	chr5:61601128-61601178	NB4	blood:	n/a
48	chr5:61598126-61598176	PFSK-1	brain:	n/a
49	chr5:61601128-61601178	CMK	blood:	n/a
50	chr5:61598126-61598176	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:61595104..61596657-chr5:61598306..61600036,2	K562	blood:
2	chr5:61593561..61597779-chr5:61600358..61604889,4	MCF-7	breast:
3	chr5:61595104..61596657-chr5:61598306..61600036,2	K562	blood:
4	chr5:61593907..61596215-chr5:61600373..61603164,3	K562	blood:
5	chr5:61561179..61563178-chr5:61595838..61598010,2	K562	blood:
6	chr5:61581288..61583777-chr5:61597562..61600246,2	K562	blood:
7	chr5:61593407..61596088-chr5:61596627..61599078,2	K562	blood:
8	chr5:61593661..61595529-chr5:61600373..61601956,2	K562	blood:
9	chr5:61560375..61564102-chr5:61592918..61596892,3	K562	blood:

Variant related genes	Relation type
KIF2A	TF binding region
KIF2A	CpG island
ENSG00000068796	chromatin interactions

Extended variants
information (count: 179 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:179 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532381310	chr5:61596239-61596240	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs551894533	chr5:61596271-61596272	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs569960274	chr5:61596307-61596308	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs189459976	chr5:61596316-61596317	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs552382600	chr5:61596317-61596318	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs181941970	chr5:61596390-61596391	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs34561011	chr5:61596391-61596392	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs534388876	chr5:61596446-61596447	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs554560832	chr5:61596487-61596488	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs368937482	chr5:61596512-61596513	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs567919264	chr5:61596596-61596597	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs540322076	chr5:61596610-61596611	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs570096360	chr5:61596615-61596616	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs537553426	chr5:61596658-61596659	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs186157110	chr5:61596684-61596685	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs577107005	chr5:61596750-61596751	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs546016580	chr5:61596808-61596809	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs553262790	chr5:61596863-61596864	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs567669380	chr5:61596864-61596865	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs573301757	chr5:61596871-61596872	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs190520299	chr5:61596921-61596922	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs397884560	chr5:61596941-61596942	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs151140981	chr5:61596959-61596960	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs71590891	chr5:61596960-61596961	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs13157549	chr5:61596962-61596963	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs113719780	chr5:61596963-61596964	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs201396632	chr5:61596964-61596965	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs377222715	chr5:61596974-61596975	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs35688674	chr5:61596977-61596978	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs541917778	chr5:61597045-61597046	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs534961612	chr5:61597135-61597136	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs181639890	chr5:61597145-61597146	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs577801477	chr5:61597146-61597147	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs530854584	chr5:61597186-61597187	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs60168826	chr5:61597234-61597235	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs3892140	chr5:61597247-61597248	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs186520910	chr5:61597340-61597341	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs191330119	chr5:61597367-61597368	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs532423941	chr5:61597413-61597414	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs552419953	chr5:61597449-61597450	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs565698489	chr5:61597488-61597489	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs528194642	chr5:61597513-61597514	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs113866547	chr5:61597562-61597563	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs556635259	chr5:61597594-61597595	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs114371812	chr5:61597635-61597636	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs116052416	chr5:61597641-61597642	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs556517666	chr5:61597645-61597646	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs116660027	chr5:61597646-61597647	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs182696734	chr5:61597661-61597662	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs58250254	chr5:61597720-61597721	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:92)

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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	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
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	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
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
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:61591400-61597200	Enhancers	Primary T cells fromperipheralblood	blood
2	chr5:61591800-61596800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr5:61592000-61596800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr5:61592000-61597400	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr5:61592800-61596800	Enhancers	Fetal Thymus	thymus
6	chr5:61593200-61596800	Enhancers	Primary T cells from cord blood	blood
7	chr5:61594800-61596200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr5:61594800-61596800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
9	chr5:61595000-61596200	Enhancers	Thymus	Thymus
10	chr5:61595200-61596200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr5:61595200-61596200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
12	chr5:61595200-61596200	Enhancers	Dnd41	blood
13	chr5:61595400-61596200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
14	chr5:61595600-61596200	Enhancers	Placenta	Placenta
15	chr5:61596000-61596200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
16	chr5:61596000-61596800	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr5:61596000-61596800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr5:61596000-61596800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr5:61596000-61596800	Enhancers	Primary T killer memory cells from peripheral blood	blood
20	chr5:61596200-61596800	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr5:61596200-61597000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr5:61596200-61600800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr5:61596200-61600800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr5:61596200-61600800	Weak transcription	Dnd41	blood
25	chr5:61596200-61601000	Weak transcription	Placenta	Placenta
26	chr5:61596200-61601000	Weak transcription	Thymus	Thymus
27	chr5:61596200-61601200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr5:61596800-61600400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr5:61596800-61600400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr5:61596800-61600400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr5:61596800-61600600	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr5:61596800-61600800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr5:61596800-61600800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr5:61596800-61600800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr5:61596800-61600800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr5:61596800-61601000	Weak transcription	Primary T cells from cord blood	blood
37	chr5:61596800-61601000	Weak transcription	Fetal Thymus	thymus
38	chr5:61597000-61599400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr5:61597200-61597600	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr5:61597400-61600400	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr5:61597600-61597800	Enhancers	Primary T cells fromperipheralblood	blood
42	chr5:61597800-61600600	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr5:61598800-61599000	Enhancers	Brain Germinal Matrix	brain
44	chr5:61599400-61601000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
45	chr5:61600200-61601000	Weak transcription	GM12878-XiMat	blood
46	chr5:61600400-61601000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr5:61600400-61601000	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr5:61600400-61601000	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr5:61600400-61601200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr5:61600600-61601000	Enhancers	Primary T helper cells PMA-I stimulated	--

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