Variant report

Variant	nsv1033140
Chromosome Location	chr5:116035131-116314673
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1951)
CpG islands
(count:854)
Chromatin interactive
region (count:21)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1951 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:116194659-116194984	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:116198385-116200736	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:116102107-116102543	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:116104996-116105536	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:116101168-116101512	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:116217836-116218042	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:116135107-116135388	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:116283657-116283951	HepG2	liver:	n/a	n/a
9	ATF1	chr5:116102266-116102552	K562	blood:	n/a	n/a
10	ATF2	chr5:116040484-116040840	GM12878	blood:	n/a	n/a
11	ATF2	chr5:116258221-116258693	GM12878	blood:	n/a	n/a
12	ATF2	chr5:116102043-116102677	GM12878	blood:	n/a	n/a
13	ATF2	chr5:116099450-116100317	GM12878	blood:	n/a	n/a
14	ATF2	chr5:116283643-116284032	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr5:116099485-116100318	GM12878	blood:	n/a	n/a
16	ATF2	chr5:116044698-116045107	GM12878	blood:	n/a	n/a
17	ATF2	chr5:116200059-116200723	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr5:116040340-116040904	GM12878	blood:	n/a	n/a
19	ATF2	chr5:116219491-116220039	GM12878	blood:	n/a	n/a
20	ATF2	chr5:116283536-116283941	GM12878	blood:	n/a	n/a
21	ATF2	chr5:116098877-116099341	GM12878	blood:	n/a	n/a
22	ATF2	chr5:116038413-116038924	GM12878	blood:	n/a	n/a
23	ATF2	chr5:116101965-116102666	GM12878	blood:	n/a	n/a
24	ATF2	chr5:116283512-116283962	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr5:116200021-116200818	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr5:116038296-116038886	GM12878	blood:	n/a	n/a
27	ATF2	chr5:116098888-116099364	GM12878	blood:	n/a	n/a
28	ATF3	chr5:116102244-116102534	K562	blood:	n/a	n/a
29	ATF3	chr5:116102087-116102580	HCT-116	colon:	n/a	n/a
30	BACH1	chr5:116283620-116284007	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr5:116099882-116099886	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr5:116095642-116096244	H1-hESC	embryonic stem cell:	n/a	n/a
33	BATF	chr5:116219676-116219912	GM12878	blood:	n/a	n/a
34	BATF	chr5:116099619-116100032	GM12878	blood:	n/a	n/a
35	BATF	chr5:116098647-116098889	GM12878	blood:	n/a	n/a
36	BATF	chr5:116221539-116221782	GM12878	blood:	n/a	n/a
37	BATF	chr5:116099641-116100251	GM12878	blood:	n/a	n/a
38	BATF	chr5:116241552-116241844	GM12878	blood:	n/a	n/a
39	BATF	chr5:116076654-116076931	GM12878	blood:	n/a	n/a
40	BATF	chr5:116241581-116241886	GM12878	blood:	n/a	n/a
41	BATF	chr5:116040310-116040833	GM12878	blood:	n/a	n/a
42	BATF	chr5:116102216-116102643	GM12878	blood:	n/a	chr5:116102437-116102448 chr5:116102419-116102430
43	BATF	chr5:116054036-116054315	GM12878	blood:	n/a	n/a
44	BATF	chr5:116038412-116038843	GM12878	blood:	n/a	n/a
45	BATF	chr5:116038442-116038823	GM12878	blood:	n/a	n/a
46	BATF	chr5:116102192-116102652	GM12878	blood:	n/a	chr5:116102437-116102448 chr5:116102419-116102430
47	BATF	chr5:116044769-116045242	GM12878	blood:	n/a	n/a
48	BCL11A	chr5:116244258-116244573	GM12878	blood:	n/a	n/a
49	BCL11A	chr5:116259165-116259363	H1-hESC	embryonic stem cell:	n/a	n/a
50	BCL11A	chr5:116200117-116200535	H1-hESC	embryonic stem cell:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:116280275-116280325	HRCEpiC	kidney:	n/a
2	chr5:116075820-116075870	HUVEC	blood vessel:	n/a
3	chr5:116274667-116274717	SK-N-SH	brain:	n/a
4	chr5:116197864-116197914	MCF10A-Er-Src	breast:	n/a
5	chr5:116113889-116113939	HCT-116	colon:	n/a
6	chr5:116039174-116039224	SK-N-SH_RA	brain:	n/a
7	chr5:116197864-116197914	AoSMC	blood vessel:	n/a
8	chr5:116274667-116274717	NH-A	brain:	n/a
9	chr5:116197864-116197914	HNPCEpiC	eye:	n/a
10	chr5:116280275-116280325	SK-N-SH	brain:	n/a
11	chr5:116197864-116197914	HRPEpiC	eye:	n/a
12	chr5:116039174-116039224	K562	blood:	n/a
13	chr5:116069988-116070038	HMEC	breast:	n/a
14	chr5:116259413-116259463	AG09319	gingival:	n/a
15	chr5:116113889-116113939	SKMC	muscle:	n/a
16	chr5:116191725-116191775	NHDF-neo	bronchial:	n/a
17	chr5:116089180-116089230	ECC-1	luminal epithelium:	n/a
18	chr5:116113889-116113939	LNCaP	prostate:	n/a
19	chr5:116069988-116070038	AG09309	skin:	n/a
20	chr5:116197864-116197914	BJ	skin:	n/a
21	chr5:116191725-116191775	ovcar-3	ovarian:	n/a
22	chr5:116306180-116306230	Hepatocyte	liver:	n/a
23	chr5:116108611-116108661	Jurkat	blood:	n/a
24	chr5:116197864-116197914	H1-hESC	embryonic stem cell:	embryo
25	chr5:116069988-116070038	HAEpiC	amniotic membrane:	n/a
26	chr5:116113889-116113939	SK-N-MC	brain:	n/a
27	chr5:116289441-116289491	HEEpiC	esophagus:	n/a
28	chr5:116280275-116280325	NB4	blood:	n/a
29	chr5:116197864-116197914	HEK293	kidney:	embryo
30	chr5:116108611-116108661	Caco-2	colon:	n/a
31	chr5:116150282-116150332	SK-N-SH_RA	brain:	n/a
32	chr5:116075820-116075870	GM12892	blood:	n/a
33	chr5:116108611-116108661	NH-A	brain:	n/a
34	chr5:116306180-116306230	HEK293	kidney:	embryo
35	chr5:116069988-116070038	AoSMC	blood vessel:	n/a
36	chr5:116191725-116191775	RPTEC	kidney:	n/a
37	chr5:116113889-116113939	AG10803	skin:	n/a
38	chr5:116089180-116089230	HCPEpiC	choroid plexus:	n/a
39	chr5:116259413-116259463	HepG2	liver:	n/a
40	chr5:116191725-116191775	GM19239	blood:	n/a
41	chr5:116197864-116197914	T-47D	breast:	n/a
42	chr5:116075820-116075870	NH-A	brain:	n/a
43	chr5:116197864-116197914	Hepatocyte	liver:	n/a
44	chr5:116280275-116280325	LNCaP	prostate:	n/a
45	chr5:116075820-116075870	SK-N-MC	brain:	n/a
46	chr5:116069988-116070038	NB4	blood:	n/a
47	chr5:116069988-116070038	GM19239	blood:	n/a
48	chr5:116108611-116108661	HIPEpiC	eye:	n/a
49	chr5:116069988-116070038	LNCaP	prostate:	n/a
50	chr5:116197864-116197914	IMR90	lung:	fetal

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:116312973..116314849-chr6:26196221..26198277,2	K562	blood:
2	chr5:116274317..116277091-chr5:116277592..116280132,2	MCF-7	breast:
3	chr5:116197562..116200213-chr5:116281914..116283961,2	MCF-7	breast:
4	chr5:115910211..115911945-chr5:116200966..116203942,2	MCF-7	breast:
5	chr3:155925817..155926573-chr5:116060845..116061700,2	MCF-7	breast:
6	chr5:116073007..116074570-chr5:116076302..116077894,2	K562	blood:
7	chr5:116073007..116074570-chr5:116076302..116077894,2	K562	blood:
8	chr5:115473291..115473804-chr5:116283477..116284254,2	MCF-7	breast:
9	chr1:17233138..17234733-chr5:116082626..116084126,2	MCF-7	breast:
10	chr1:144532509..144534121-chr5:116081146..116082646,2	K562	blood:
11	chr5:115911257..115912668-chr5:116283296..116284268,6	MCF-7	breast:
12	chr5:116052297..116054346-chr5:116056062..116057834,2	K562	blood:
13	chr5:116274317..116277091-chr5:116277592..116280132,2	MCF-7	breast:
14	chr5:116052297..116054346-chr5:116056062..116057834,2	K562	blood:
15	chr5:116159664..116161786-chr5:116162291..116165318,3	MCF-7	breast:
16	chr5:116141325..116143664-chr5:116165603..116167947,2	K562	blood:
17	chr5:116159664..116161786-chr5:116162291..116165318,3	MCF-7	breast:
18	chr5:116216466..116219443-chr5:116220949..116224827,3	MCF-7	breast:
19	chr5:116197562..116200213-chr5:116281914..116283961,2	MCF-7	breast:
20	chr5:116216466..116219443-chr5:116220949..116224827,3	MCF-7	breast:
21	chr5:115911320..115912473-chr5:116283341..116284236,4	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COMMD10-10	chr5:116145051-116147613	NONHSAT103378
2	lnc-SEMA6A-3	chr5:116078998-116079084	NR_104678
3	lnc-COMMD10-11	chr5:116282030-116282143	NONHSAT103381
4	lnc-SEMA6A-3	chr5:116078687-116079084	XLOC_004962
5	lnc-SEMA6A-6	chr5:116040765-116040866	NONHSAT103376
6	lnc-COMMD10-10	chr5:116143614-116143900	NONHSAT103378
7	lnc-COMMD10-11	chr5:116281744-116281873	NONHSAT103381
8	lnc-SEMA6A-3	chr5:116096591-116096711	XLOC_004962
9	lnc-SEMA6A-6	chr5:116040765-116040866	FPKM1_group_26180_transcript_1
10	lnc-COMMD10-10	chr5:116147785-116149816	NONHSAT103378
11	lnc-SEMA6A-3	chr5:116096379-116096485	XLOC_004962
12	lnc-SEMA6A-3	chr5:116096591-116096711	NR_104678
13	lnc-SEMA6A-3	chr5:116097825-116097905	NR_104678
14	lnc-SEMA6A-3	chr5:116096379-116096485	NR_104678
15	lnc-SEMA6A-3	chr5:116097825-116097905	XLOC_004962

No data

Variant related genes	Relation type
ENSG00000251311	TF binding region
ENSG00000249150	TF binding region
RPS17P2	TF binding region
ENSG00000251311	CpG island
ENSG00000249150	CpG island
RPS17P2	CpG island
ENSG00000092421	chromatin interactions
ENSG00000249150	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000197409	chromatin interactions

Extended variants
information (count: 11013 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:11013 , 50 per page) page: 1 2 3 4 5 6 7 ... 221

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533207901	chr5:116035159-116035160	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs7730002	chr5:116035166-116035167	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs560158530	chr5:116035187-116035188	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs117574915	chr5:116035195-116035196	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs549076638	chr5:116035200-116035201	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs568966391	chr5:116035238-116035239	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs183347977	chr5:116035246-116035247	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs368936788	chr5:116035276-116035277	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs34809928	chr5:116035281-116035282	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs200942269	chr5:116035283-116035284	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs4920930	chr5:116035284-116035285	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs200249725	chr5:116035285-116035286	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs371074930	chr5:116035291-116035292	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs397884051	chr5:116035297-116035298	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs143006153	chr5:116035345-116035346	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs534180768	chr5:116035395-116035396	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs554057338	chr5:116035403-116035404	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs150664756	chr5:116035405-116035406	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs367859808	chr5:116035411-116035412	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs556376578	chr5:116035530-116035531	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs576530022	chr5:116035531-116035532	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs187835153	chr5:116035538-116035539	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs2933647	chr5:116035540-116035541	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs375454737	chr5:116035547-116035548	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs13354807	chr5:116035551-116035552	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs574121927	chr5:116035566-116035567	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs570922382	chr5:116035575-116035576	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs540506930	chr5:116035658-116035659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560472345	chr5:116035666-116035667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs564201688	chr5:116035693-116035694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs193160867	chr5:116035698-116035699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs75638953	chr5:116035700-116035701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs10044521	chr5:116035707-116035708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531386920	chr5:116035712-116035713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551194191	chr5:116035754-116035755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs56702552	chr5:116035797-116035798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs73263308	chr5:116035821-116035822	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs201604471	chr5:116035822-116035823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534143262	chr5:116035834-116035835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs369524807	chr5:116035836-116035837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs76137082	chr5:116035838-116035839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547670891	chr5:116035879-116035880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567661594	chr5:116035885-116035886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556722345	chr5:116035923-116035924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535687744	chr5:116035969-116035970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556476569	chr5:116035983-116035984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576368785	chr5:116035998-116035999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556955628	chr5:116036011-116036012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs184984354	chr5:116036012-116036013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs189636119	chr5:116036013-116036014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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
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
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	21215367	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1639 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116032400-116040600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:116032600-116038200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr5:116032800-116038200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr5:116032800-116038200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr5:116032800-116038200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr5:116032800-116038200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr5:116033000-116038400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr5:116034800-116035600	Enhancers	Fetal Lung	lung
9	chr5:116035000-116035600	Flanking Active TSS	GM12878-XiMat	blood
10	chr5:116035600-116036800	Enhancers	GM12878-XiMat	blood
11	chr5:116036800-116037400	Weak transcription	GM12878-XiMat	blood
12	chr5:116037400-116040200	Enhancers	GM12878-XiMat	blood
13	chr5:116037600-116037800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr5:116037800-116040600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr5:116038200-116038400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr5:116038200-116038800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr5:116038200-116040400	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr5:116038200-116041400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr5:116038200-116041400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr5:116038200-116042200	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr5:116038400-116038800	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr5:116038400-116038800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr5:116038400-116039200	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr5:116038400-116041000	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr5:116038400-116042000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr5:116038600-116041000	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr5:116038800-116039800	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr5:116039000-116039200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr5:116039200-116041200	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr5:116039200-116041800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr5:116039800-116040000	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr5:116040000-116040400	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr5:116040200-116040400	Flanking Active TSS	GM12878-XiMat	blood
34	chr5:116040400-116040800	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr5:116040400-116040800	Active TSS	GM12878-XiMat	blood
36	chr5:116040400-116041800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr5:116040600-116040800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr5:116040600-116040800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr5:116040800-116045400	Enhancers	GM12878-XiMat	blood
40	chr5:116041000-116041600	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr5:116041600-116041800	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr5:116041800-116042000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr5:116041800-116044000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr5:116042800-116043000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr5:116044000-116045000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr5:116044400-116044600	Enhancers	Rectal Smooth Muscle	rectum
47	chr5:116044600-116045800	Weak transcription	Rectal Smooth Muscle	rectum
48	chr5:116045200-116045400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr5:116045400-116046200	ZNF genes & repeats	GM12878-XiMat	blood
50	chr5:116045800-116046200	Enhancers	Rectal Smooth Muscle	rectum

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