Variant report

Variant	nsv528467
Chromosome Location	chrX:105278361-105354377
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	ARID3A	chrX:105282567-105283059	HepG2	liver:	n/a	n/a
2	BACH1	chrX:105314219-105314360	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chrX:105299863-105300103	GM12878	blood:	n/a	chrX:105299965-105299976
4	BATF	chrX:105299907-105300053	GM12878	blood:	n/a	chrX:105299965-105299976
5	CEBPB	chrX:105313125-105313328	H1-hESC	embryonic stem cell:	n/a	chrX:105313231-105313242
6	CEBPB	chrX:105282639-105282873	HepG2	liver:	n/a	chrX:105282759-105282770 chrX:105282757-105282768 chrX:105282660-105282672 chrX:105282757-105282770 chrX:105282759-105282770
7	CEBPB	chrX:105313056-105313427	IMR90	lung:	n/a	chrX:105313231-105313242
8	CEBPB	chrX:105313063-105313388	A549	lung:	n/a	chrX:105313231-105313242
9	CEBPB	chrX:105282591-105282944	HepG2	liver:	n/a	chrX:105282759-105282770 chrX:105282757-105282768 chrX:105282660-105282672 chrX:105282757-105282770 chrX:105282759-105282770
10	CEBPB	chrX:105282572-105282980	HepG2	liver:	n/a	chrX:105282759-105282770 chrX:105282757-105282768 chrX:105282660-105282672 chrX:105282757-105282770 chrX:105282759-105282770
11	CEBPB	chrX:105313066-105313398	HepG2	liver:	n/a	chrX:105313231-105313242
12	CEBPB	chrX:105313071-105313395	K562	blood:	n/a	chrX:105313231-105313242
13	CEBPB	chrX:105282573-105282961	HepG2	liver:	n/a	chrX:105282759-105282770 chrX:105282757-105282768 chrX:105282660-105282672 chrX:105282757-105282770 chrX:105282759-105282770
14	CEBPB	chrX:105289026-105289247	HepG2	liver:	n/a	chrX:105289106-105289117 chrX:105289210-105289227
15	CTCF	chrX:105279200-105279350	A549	lung:	n/a	n/a
16	CTCF	chrX:105279180-105279330	GM12864	blood:	n/a	n/a
17	CTCF	chrX:105279180-105279330	GM12875	blood:	n/a	n/a
18	CTCF	chrX:105298769-105298827	Medullo	brain:	n/a	n/a
19	CTCF	chrX:105279166-105279348	HepG2	liver:	n/a	n/a
20	CTCF	chrX:105284028-105284214	Hela-S3	cervix:	n/a	chrX:105284108-105284118 chrX:105284105-105284123 chrX:105284107-105284120 chrX:105284106-105284122 chrX:105284111-105284120 chrX:105284100-105284121
21	CTCF	chrX:105279177-105279342	GM13977	blood:	n/a	n/a
22	CTCF	chrX:105279200-105279350	HEEpiC	esophagus:	n/a	n/a
23	CTCF	chrX:105284059-105284190	Gliobla	brain:	n/a	chrX:105284108-105284118 chrX:105284105-105284123 chrX:105284107-105284120 chrX:105284106-105284122 chrX:105284111-105284120 chrX:105284100-105284121
24	CTCF	chrX:105279125-105279379	GM12878	blood:	n/a	n/a
25	CTCF	chrX:105284040-105284190	GM12864	blood:	n/a	chrX:105284108-105284118 chrX:105284105-105284123 chrX:105284107-105284120 chrX:105284106-105284122 chrX:105284111-105284120 chrX:105284100-105284121
26	CTCF	chrX:105284000-105284150	GM12872	blood:	n/a	chrX:105284108-105284118 chrX:105284105-105284123 chrX:105284107-105284120 chrX:105284106-105284122 chrX:105284111-105284120 chrX:105284100-105284121
27	CTCF	chrX:105279179-105279307	A549	lung:	n/a	n/a
28	CTCF	chrX:105279200-105279350	MCF-7	breast:	n/a	n/a
29	CTCF	chrX:105284006-105284250	MCF-7	breast:	n/a	chrX:105284108-105284118 chrX:105284105-105284123 chrX:105284107-105284120 chrX:105284106-105284122 chrX:105284111-105284120 chrX:105284100-105284121
30	CTCF	chrX:105279215-105279272	Fibrobl	skin:	n/a	n/a
31	CTCF	chrX:105279200-105279350	HEK293	kidney:	n/a	n/a
32	CTCF	chrX:105279180-105279330	GM12870	blood:	n/a	n/a
33	CTCF	chrX:105284040-105284190	HA-sp	spinal cord:	n/a	chrX:105284108-105284118 chrX:105284105-105284123 chrX:105284107-105284120 chrX:105284106-105284122 chrX:105284111-105284120 chrX:105284100-105284121
34	CTCF	chrX:105279160-105279310	HL-60	blood:	n/a	n/a
35	CTCF	chrX:105353791-105353823	GM10248	blood:	n/a	n/a
36	CTCF	chrX:105283952-105284288	IMR90	lung:	n/a	chrX:105284108-105284118 chrX:105284105-105284123 chrX:105284107-105284120 chrX:105284106-105284122 chrX:105284111-105284120 chrX:105284100-105284121
37	CTCF	chrX:105284060-105284210	AG04450	lung:	n/a	chrX:105284108-105284118 chrX:105284105-105284123 chrX:105284107-105284120 chrX:105284106-105284122 chrX:105284111-105284120 chrX:105284100-105284121
38	CTCF	chrX:105284080-105284230	HCM	heart:	n/a	chrX:105284108-105284118 chrX:105284105-105284123 chrX:105284107-105284120 chrX:105284106-105284122 chrX:105284111-105284120 chrX:105284100-105284121
39	CTCF	chrX:105279140-105279290	SAEC	small airway:	n/a	n/a
40	CTCF	chrX:105284057-105284189	HUVEC	blood vessel:	n/a	chrX:105284108-105284118 chrX:105284105-105284123 chrX:105284107-105284120 chrX:105284106-105284122 chrX:105284111-105284120 chrX:105284100-105284121
41	CTCF	chrX:105284016-105284214	SK-N-SH_RA	brain:	n/a	chrX:105284108-105284118 chrX:105284105-105284123 chrX:105284107-105284120 chrX:105284106-105284122 chrX:105284111-105284120 chrX:105284100-105284121
42	CTCF	chrX:105284035-105284247	NHEK	skin:	n/a	chrX:105284108-105284118 chrX:105284105-105284123 chrX:105284107-105284120 chrX:105284106-105284122 chrX:105284111-105284120 chrX:105284100-105284121
43	CTCF	chrX:105279120-105279270	HCT-116	colon:	n/a	n/a
44	CTCF	chrX:105340604-105340718	GM20000	blood:	n/a	n/a
45	CTCF	chrX:105279201-105279315	GM19239	blood:	n/a	n/a
46	CTCF	chrX:105279200-105279350	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chrX:105352220-105352291	GM10248	blood:	n/a	n/a
48	CTCF	chrX:105279180-105279330	GM12872	blood:	n/a	n/a
49	CTCF	chrX:105326349-105326399	HepG2	liver:	n/a	n/a
50	CTCF	chrX:105283914-105284251	HepG2	liver:	n/a	chrX:105284108-105284118 chrX:105284105-105284123 chrX:105284107-105284120 chrX:105284106-105284122 chrX:105284111-105284120 chrX:105284100-105284121

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:105280566-105280616	HUVEC	blood vessel:	n/a
2	chrX:105280566-105280616	SK-N-MC	brain:	n/a
3	chrX:105279680-105279730	U87	brain:	n/a
4	chrX:105281285-105281335	NB4	blood:	n/a
5	chrX:105280566-105280616	GM12891	blood:	n/a
6	chrX:105280566-105280616	HRCEpiC	kidney:	n/a
7	chrX:105280886-105280936	MCF10A-Er-Src	breast:	n/a
8	chrX:105279680-105279730	ProgFib	skin:	n/a
9	chrX:105281285-105281335	ProgFib	skin:	n/a
10	chrX:105279680-105279730	ovcar-3	ovarian:	n/a
11	chrX:105281285-105281335	HCF	heart:	n/a
12	chrX:105280886-105280936	AoSMC	blood vessel:	n/a
13	chrX:105281285-105281335	SK-N-MC	brain:	n/a
14	chrX:105279680-105279730	H1-hESC	embryonic stem cell:	embryo
15	chrX:105281285-105281335	ECC-1	luminal epithelium:	n/a
16	chrX:105279680-105279730	HMEC	breast:	n/a
17	chrX:105280886-105280936	AG09309	skin:	n/a
18	chrX:105280566-105280616	SAEC	small airway:	n/a
19	chrX:105281285-105281335	SK-N-SH	brain:	n/a
20	chrX:105281285-105281335	GM19239	blood:	n/a
21	chrX:105281285-105281335	NT2-D1	testis:	n/a
22	chrX:105281285-105281335	HCPEpiC	choroid plexus:	n/a
23	chrX:105280886-105280936	HNPCEpiC	eye:	n/a
24	chrX:105281285-105281335	AG04450	lung:	fetal
25	chrX:105279680-105279730	AG09319	gingival:	n/a
26	chrX:105280886-105280936	ProgFib	skin:	n/a
27	chrX:105280886-105280936	HCT-116	colon:	n/a
28	chrX:105279680-105279730	LNCaP	prostate:	n/a
29	chrX:105281285-105281335	HRCEpiC	kidney:	n/a
30	chrX:105279680-105279730	RPTEC	kidney:	n/a
31	chrX:105279680-105279730	HRPEpiC	eye:	n/a
32	chrX:105280566-105280616	Hepatocyte	liver:	n/a
33	chrX:105279680-105279730	Hepatocyte	liver:	n/a
34	chrX:105279680-105279730	HUVEC	blood vessel:	n/a
35	chrX:105280566-105280616	H1-hESC	embryonic stem cell:	embryo
36	chrX:105279680-105279730	A549	lung:	n/a
37	chrX:105281285-105281335	PANC-1	pancreas:	n/a
38	chrX:105280566-105280616	MCF10A-Er-Src	breast:	n/a
39	chrX:105280886-105280936	AG04449	skin:	fetal
40	chrX:105281285-105281335	PrEC	prostate:	n/a
41	chrX:105281285-105281335	LNCaP	prostate:	n/a
42	chrX:105281285-105281335	BJ	skin:	n/a
43	chrX:105281285-105281335	Caco-2	colon:	n/a
44	chrX:105281285-105281335	SK-N-SH_RA	brain:	n/a
45	chrX:105280566-105280616	IMR90	lung:	fetal
46	chrX:105281285-105281335	BE2_C	brain:	n/a
47	chrX:105280566-105280616	AG04449	skin:	fetal
48	chrX:105280566-105280616	AG09309	skin:	n/a
49	chrX:105279680-105279730	NB4	blood:	n/a
50	chrX:105281285-105281335	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chrX:105219100..105220073-chrX:105283704..105284665,3	MCF-7	breast:
2	chr17:7477121..7479091-chrX:105333663..105335185,2	K562	blood:
3	chrX:105283639..105284623-chrX:105636258..105637085,3	MCF-7	breast:
4	chrX:105283749..105284515-chrX:105414167..105414952,2	MCF-7	breast:
5	chrX:105309111..105311761-chrX:105313612..105315963,2	MCF-7	breast:
6	chrX:105307192..105309274-chrX:105312648..105315064,2	K562	blood:
7	chrX:105277280..105279947-chrX:105280016..105282819,2	K562	blood:
8	chrX:105277280..105279947-chrX:105280016..105282819,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MUM1L1-1	chrX:105314472-105315213	NONHSAT138102
2	lnc-MUM1L1-1	chrX:105316683-105317193	NONHSAT138102

Variant related genes	Relation type
SERPINA7	TF binding region
ENSG00000230788	TF binding region
SERPINA7	CpG island
ENSG00000230788	CpG island
ENSG00000161960	chromatin interactions
ENSG00000230788	chromatin interactions
ENSG00000123561	chromatin interactions
ENSG00000209582	chromatin interactions

Extended variants
information (count: 373 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:373 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1804495	chrX:105278361-105278362	Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs121909496	chrX:105278371-105278372	Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs199840798	chrX:105278390-105278391	Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs370344330	chrX:105278403-105278404	Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs2234039	chrX:105278409-105278410	Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs183508470	chrX:105278458-105278459	Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs62603105	chrX:105278459-105278460	Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs186841242	chrX:105278492-105278493	Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs145676890	chrX:105278498-105278499	Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs138230709	chrX:105278516-105278517	Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs371879049	chrX:105278573-105278574	Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs75151279	chrX:105278624-105278625	Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs192092406	chrX:105278632-105278633	Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs73517294	chrX:105278633-105278634	Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs183916603	chrX:105278734-105278735	Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs17332369	chrX:105278765-105278766	Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs149521387	chrX:105278782-105278783	Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs186765037	chrX:105278784-105278785	Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs113672465	chrX:105278859-105278860	Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs36020211	chrX:105278874-105278875	Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs191610501	chrX:105278884-105278885	Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs559251511	chrX:105278953-105278954	Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs539085331	chrX:105279025-105279026	Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs2234038	chrX:105279030-105279031	Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs2234037	chrX:105279056-105279057	Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs370955959	chrX:105279057-105279058	Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375380232	chrX:105279118-105279119	Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs182605024	chrX:105279119-105279120	Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs202100037	chrX:105279136-105279137	Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs145727317	chrX:105279147-105279148	Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs148952971	chrX:105279165-105279166	Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs28937312	chrX:105279259-105279260	Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs72554660	chrX:105279272-105279273	Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs201097082	chrX:105279315-105279316	Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs368597333	chrX:105279341-105279342	Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs372899948	chrX:105279346-105279347	Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs2234036	chrX:105279368-105279369	Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs200523251	chrX:105279415-105279416	Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs2234035	chrX:105279416-105279417	Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs2234034	chrX:105279499-105279500	Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs187309675	chrX:105279539-105279540	Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs557192299	chrX:105279667-105279668	Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs144978488	chrX:105279670-105279671	Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs191836991	chrX:105279681-105279682	Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs150704715	chrX:105279716-105279717	Flanking Active TSS Transcr. at gene 5' and 3'	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs372227782	chrX:105279768-105279769	Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs370024260	chrX:105279918-105279919	Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs34792273	chrX:105280118-105280119	Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs367621131	chrX:105280411-105280412	Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs371332756	chrX:105280457-105280458	Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:49)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Astrocytoma	17387387	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	21979893	CNVD
Schizophrenia	23904455	CNVD
Olfactory neuroblastoma	18408657	CNVD
infertile	22614455	CNVD
Autism	22495311	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	22429812	CNVD
Cancer	16751803	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Multiple myeloma	17550852	CNVD
Cerebellar hypoplasia	21569638	CNVD
X-linked lissencephaly	21569638	CNVD
Pelizaeus-Merzbacher disease	18923514	CNVD
Pelizaeus-Merzbacher disease	22241247	CNVD
Cervical cancer	21062161	CNVD
Myxofibrosarcoma	16751306	CNVD
Pelizaeus-Merzbacher disease	22470819	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Astrocytoma	22246337	CNVD
Hirschsprung''s Disease	21712996	CNVD
X-linked lissencephaly	21572526	CNVD
Oligozoospermia	20877625	CNVD
Mental retardation	17406619	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:105277400-105278400	Strong transcription	HepG2	liver
2	chrX:105277600-105278800	Strong transcription	Liver	Liver
3	chrX:105278400-105279000	Genic enhancers	HepG2	liver
4	chrX:105278800-105279200	Genic enhancers	Liver	Liver
5	chrX:105279000-105280600	Transcr. at gene 5' and 3'	HepG2	liver
6	chrX:105279200-105279400	Transcr. at gene 5' and 3'	Liver	Liver
7	chrX:105279400-105279800	Flanking Active TSS	Liver	Liver
8	chrX:105279800-105280000	Active TSS	Liver	Liver
9	chrX:105280000-105280200	Flanking Active TSS	Liver	Liver
10	chrX:105280200-105280600	Active TSS	Liver	Liver
11	chrX:105280600-105281400	Flanking Active TSS	Liver	Liver
12	chrX:105280600-105283200	Active TSS	HepG2	liver
13	chrX:105281400-105282800	Active TSS	Liver	Liver
14	chrX:105282000-105284000	Enhancers	Fetal Intestine Large	intestine
15	chrX:105282000-105284000	Enhancers	Fetal Intestine Small	intestine
16	chrX:105282800-105283200	Flanking Active TSS	Liver	Liver
17	chrX:105283200-105283600	Flanking Active TSS	HepG2	liver
18	chrX:105283200-105284600	Enhancers	Liver	Liver
19	chrX:105283600-105285000	Enhancers	HepG2	liver
20	chrX:105283800-105284000	Bivalent Enhancer	Ovary	ovary
21	chrX:105283800-105284400	Enhancers	Pancreas	Pancrea
22	chrX:105284600-105288400	Weak transcription	Liver	Liver
23	chrX:105286400-105286800	Enhancers	Rectal Smooth Muscle	rectum
24	chrX:105288400-105289400	Enhancers	Liver	Liver
25	chrX:105297800-105299200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chrX:105298000-105298600	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chrX:105298200-105298600	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chrX:105298200-105299000	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chrX:105298600-105299000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chrX:105299000-105299600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chrX:105312200-105313000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chrX:105320400-105320600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
33	chrX:105333400-105334200	Enhancers	HepG2	liver

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