Variant report

Variant	nsv549205
Chromosome Location	chr1:217165548-217270219
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	chr1:217178845-217178930	K562	blood:	n/a	n/a
2	ATF2	chr1:217178120-217178438	GM12878	blood:	n/a	n/a
3	ATF2	chr1:217200734-217201124	GM12878	blood:	n/a	n/a
4	ATF2	chr1:217200716-217201206	GM12878	blood:	n/a	n/a
5	ATF2	chr1:217221682-217222024	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr1:217183691-217183866	GM12878	blood:	n/a	chr1:217183786-217183797 chr1:217183787-217183797
7	BATF	chr1:217241049-217241308	GM12878	blood:	n/a	n/a
8	BATF	chr1:217200788-217201121	GM12878	blood:	n/a	chr1:217200994-217201002
9	BATF	chr1:217178158-217178539	GM12878	blood:	n/a	n/a
10	BCL11A	chr1:217200669-217201164	GM12878	blood:	n/a	chr1:217200921-217200930
11	BCL11A	chr1:217200644-217201158	GM12878	blood:	n/a	chr1:217200921-217200930
12	BCL3	chr1:217200819-217201040	GM12878	blood:	n/a	chr1:217200921-217200930
13	BCL3	chr1:217178169-217178445	GM12878	blood:	n/a	n/a
14	BCL3	chr1:217220035-217220359	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:217250108-217250151	K562	blood:	n/a	n/a
16	BHLHE40	chr1:217200687-217201179	GM12878	blood:	n/a	n/a
17	CEBPB	chr1:217238815-217239285	A549	lung:	n/a	n/a
18	CEBPB	chr1:217206020-217206360	MCF-7	breast:	n/a	chr1:217206201-217206210 chr1:217206201-217206210 chr1:217206201-217206210 chr1:217206200-217206211 chr1:217206201-217206210 chr1:217206199-217206212
19	CEBPB	chr1:217206016-217206380	A549	lung:	n/a	chr1:217206201-217206210 chr1:217206201-217206210 chr1:217206201-217206210 chr1:217206200-217206211 chr1:217206201-217206210 chr1:217206199-217206212
20	CEBPB	chr1:217249283-217249561	HepG2	liver:	n/a	chr1:217249415-217249426
21	CEBPB	chr1:217171384-217171558	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr1:217202530-217203110	HCT-116	colon:	n/a	n/a
23	CEBPB	chr1:217221577-217221841	A549	lung:	n/a	chr1:217221684-217221695
24	CEBPB	chr1:217191036-217191349	IMR90	lung:	n/a	chr1:217191191-217191202
25	CEBPB	chr1:217261733-217262128	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:217202616-217203385	IMR90	lung:	n/a	n/a
27	CEBPB	chr1:217249318-217249496	H1-hESC	embryonic stem cell:	n/a	chr1:217249415-217249426
28	CEBPB	chr1:217221509-217221872	IMR90	lung:	n/a	chr1:217221684-217221695
29	CEBPB	chr1:217191034-217191331	HepG2	liver:	n/a	chr1:217191191-217191202
30	CEBPB	chr1:217206044-217206347	Hela-S3	cervix:	n/a	chr1:217206201-217206210 chr1:217206201-217206210 chr1:217206201-217206210 chr1:217206200-217206211 chr1:217206201-217206210 chr1:217206199-217206212
31	CEBPB	chr1:217202866-217202964	K562	blood:	n/a	n/a
32	CEBPB	chr1:217239102-217239142	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr1:217200675-217201161	GM12878	blood:	n/a	n/a
34	CEBPB	chr1:217177029-217177213	K562	blood:	n/a	chr1:217177074-217177087 chr1:217177076-217177087
35	CEBPB	chr1:217202594-217203143	HCT-116	colon:	n/a	n/a
36	CEBPB	chr1:217206068-217206359	H1-hESC	embryonic stem cell:	n/a	chr1:217206201-217206210 chr1:217206201-217206210 chr1:217206201-217206210 chr1:217206200-217206211 chr1:217206201-217206210 chr1:217206199-217206212
37	CEBPB	chr1:217202719-217203060	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr1:217202681-217203080	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr1:217221611-217221811	K562	blood:	n/a	chr1:217221684-217221695
40	CEBPB	chr1:217221526-217222040	MCF-7	breast:	n/a	chr1:217221684-217221695
41	CEBPB	chr1:217193677-217193854	HepG2	liver:	n/a	chr1:217193712-217193723
42	CEBPB	chr1:217249391-217249437	K562	blood:	n/a	chr1:217249415-217249426
43	CEBPB	chr1:217202523-217203418	MCF-7	breast:	n/a	n/a
44	CEBPB	chr1:217238950-217239228	HepG2	liver:	n/a	n/a
45	CEBPB	chr1:217202703-217202968	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr1:217241283-217241320	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr1:217206024-217206389	HepG2	liver:	n/a	chr1:217206201-217206210 chr1:217206201-217206210 chr1:217206201-217206210 chr1:217206200-217206211 chr1:217206201-217206210 chr1:217206199-217206212
48	CEBPB	chr1:217262748-217263532	MCF-7	breast:	n/a	n/a
49	CEBPB	chr1:217202448-217203254	MCF-7	breast:	n/a	n/a
50	CEBPB	chr1:217206020-217206385	IMR90	lung:	n/a	chr1:217206201-217206210 chr1:217206201-217206210 chr1:217206201-217206210 chr1:217206200-217206211 chr1:217206201-217206210 chr1:217206199-217206212

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:217262892-217262942	GM19239	blood:	n/a
2	chr1:217263805-217263855	ProgFib	skin:	n/a
3	chr1:217262892-217262942	GM19239	blood:	n/a
4	chr1:217263805-217263855	ProgFib	skin:	n/a
5	chr1:217168635-217168685	SKMC	muscle:	n/a
6	chr1:217265862-217265912	HRE	kidney:	n/a
7	chr1:217203173-217203223	HCF	heart:	n/a
8	chr1:217170675-217170725	NB4	blood:	n/a
9	chr1:217261949-217261999	HIPEpiC	eye:	n/a
10	chr1:217263507-217263557	Jurkat	blood:	n/a
11	chr1:217263621-217263671	AG10803	skin:	n/a
12	chr1:217262892-217262942	ovcar-3	ovarian:	n/a
13	chr1:217168635-217168685	HepG2	liver:	n/a
14	chr1:217263621-217263671	U87	brain:	n/a
15	chr1:217241497-217241547	AG09309	skin:	n/a
16	chr1:217263805-217263855	HCM	heart:	n/a
17	chr1:217263507-217263557	PANC-1	pancreas:	n/a
18	chr1:217168635-217168685	U87	brain:	n/a
19	chr1:217263847-217263897	IMR90	lung:	fetal
20	chr1:217263507-217263557	LNCaP	prostate:	n/a
21	chr1:217263621-217263671	K562	blood:	n/a
22	chr1:217263847-217263897	GM12878	blood:	n/a
23	chr1:217170675-217170725	Caco-2	colon:	n/a
24	chr1:217241497-217241547	HIPEpiC	eye:	n/a
25	chr1:217263847-217263897	LNCaP	prostate:	n/a
26	chr1:217170675-217170725	HEK293	kidney:	embryo
27	chr1:217263213-217263263	HEEpiC	esophagus:	n/a
28	chr1:217263847-217263897	HRPEpiC	eye:	n/a
29	chr1:217262892-217262942	HepG2	liver:	n/a
30	chr1:217263213-217263263	SK-N-MC	brain:	n/a
31	chr1:217263805-217263855	Caco-2	colon:	n/a
32	chr1:217263621-217263671	LNCaP	prostate:	n/a
33	chr1:217263621-217263671	AoSMC	blood vessel:	n/a
34	chr1:217262889-217262939	HCT-116	colon:	n/a
35	chr1:217203173-217203223	BE2_C	brain:	n/a
36	chr1:217263621-217263671	GM12891	blood:	n/a
37	chr1:217263805-217263855	Hela-S3	cervix:	n/a
38	chr1:217170675-217170725	NHDF-neo	bronchial:	n/a
39	chr1:217265862-217265912	Hela-S3	cervix:	n/a
40	chr1:217262889-217262939	ProgFib	skin:	n/a
41	chr1:217262892-217262942	NH-A	brain:	n/a
42	chr1:217203173-217203223	ProgFib	skin:	n/a
43	chr1:217263805-217263855	HEK293	kidney:	embryo
44	chr1:217262889-217262939	HPAEpiC	pulmonary alveolar:	n/a
45	chr1:217263213-217263263	SK-N-SH	brain:	n/a
46	chr1:217263847-217263897	SAEC	small airway:	n/a
47	chr1:217263847-217263897	HIPEpiC	eye:	n/a
48	chr1:217241497-217241547	AG04450	lung:	fetal
49	chr1:217262892-217262942	GM12878	blood:	n/a
50	chr1:217262978-217263028	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr1:217167662..217170376-chr1:217171384..217173746,2	MCF-7	breast:
2	chr1:151490362..151490900-chr1:217221528..217222303,2	MCF-7	breast:
3	chr1:217167481..217170396-chr1:217191288..217193517,2	MCF-7	breast:
4	chr1:217177180..217179846-chr1:217183468..217185812,2	K562	blood:
5	chr1:217221077..217222358-chr1:217507021..217508605,8	MCF-7	breast:
6	chr1:217261995..217264786-chr1:217266370..217270412,4	MCF-7	breast:
7	chr1:217221528..217222278-chr20:49077016..49077556,2	MCF-7	breast:
8	chr1:217215201..217218103-chr1:217218640..217221582,2	MCF-7	breast:
9	chr1:217221387..217222141-chr1:217752526..217753081,2	MCF-7	breast:
10	chr1:217249153..217251039-chr1:217255298..217256845,2	MCF-7	breast:
11	chr1:217215201..217218103-chr1:217218640..217221582,2	MCF-7	breast:
12	chr1:217233709..217236581-chr1:217238829..217241091,2	MCF-7	breast:
13	chr1:217177180..217179846-chr1:217183468..217185812,2	K562	blood:
14	chr1:217261026..217264495-chr1:217266282..217268248,3	K562	blood:
15	chr1:217167481..217170396-chr1:217191288..217193517,2	MCF-7	breast:
16	chr1:217233709..217236581-chr1:217238829..217241091,2	MCF-7	breast:
17	chr1:217221377..217221879-chr1:217505790..217506706,2	MCF-7	breast:
18	chr1:217235815..217237725-chr1:217308082..217309758,2	MCF-7	breast:
19	chr1:217200941..217201873-chr6:54053550..54054293,2	MCF-7	breast:
20	chr1:217167662..217170376-chr1:217171384..217173746,2	MCF-7	breast:
21	chr1:217256324..217258384-chr1:217263313..217265542,2	K562	blood:
22	chr1:217165379..217166249-chr5:170520563..170521270,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPATCH2-6	chr1:217251478-217251702	NONHSAT009489
2	lnc-GPATCH2-6	chr1:217262849-217262978	NONHSAT009490
3	lnc-GPATCH2-6	chr1:217263773-217263889	NONHSAT009491
4	lnc-GPATCH2-6	chr1:217262849-217262955	NONHSAT009492

Variant related genes	Relation type
ESRRG	TF binding region
ESRRG	CpG island
ENSG00000196482	chromatin interactions

Extended variants
information (count: 4196 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:4196 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17041541	chr1:217165548-217165549	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530516913	chr1:217165570-217165571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116473363	chr1:217165585-217165586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115775944	chr1:217165599-217165600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141646235	chr1:217165616-217165617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575560097	chr1:217165668-217165669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538019289	chr1:217165680-217165681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183908971	chr1:217165723-217165724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369995422	chr1:217165734-217165735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186776927	chr1:217165796-217165797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560428041	chr1:217165855-217165856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs116557961	chr1:217165868-217165869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545914878	chr1:217165916-217165917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs17044824	chr1:217165923-217165924	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs74141722	chr1:217165963-217165964	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs551946489	chr1:217165998-217165999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550752292	chr1:217166022-217166023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559389364	chr1:217166028-217166029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561063360	chr1:217166032-217166033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145377986	chr1:217166060-217166061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546665716	chr1:217166085-217166086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528217280	chr1:217166154-217166155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566479586	chr1:217166187-217166188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538606564	chr1:217166205-217166206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551776174	chr1:217166215-217166216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569175659	chr1:217166225-217166226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538160375	chr1:217166316-217166317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554697088	chr1:217166329-217166330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574974456	chr1:217166344-217166345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191675431	chr1:217166352-217166353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554227278	chr1:217166373-217166374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147663958	chr1:217166387-217166388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs61816709	chr1:217166417-217166418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556603849	chr1:217166428-217166429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2818768	chr1:217166460-217166461	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs544511982	chr1:217166554-217166555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539911974	chr1:217166605-217166606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182865967	chr1:217166662-217166663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78595913	chr1:217166682-217166683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540081542	chr1:217166708-217166709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560163807	chr1:217166711-217166712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2818767	chr1:217166716-217166717	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs2818766	chr1:217166744-217166745	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs17044837	chr1:217166839-217166840	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs543461516	chr1:217166860-217166861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114565806	chr1:217166902-217166903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140918909	chr1:217166910-217166911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534384627	chr1:217166952-217166953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187191742	chr1:217166991-217166992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570882823	chr1:217167083-217167084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Pancreatic cancer	17952125	CNVD
Autism	14699429	CNVD

Chromatin state (count:968 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:217157400-217194400	Weak transcription	Fetal Muscle Leg	muscle
2	chr1:217161200-217170600	Weak transcription	Pancreas	Pancrea
3	chr1:217168600-217168800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr1:217168600-217168800	Enhancers	Aorta	Aorta
5	chr1:217169000-217170600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr1:217170400-217171000	Enhancers	Brain Germinal Matrix	brain
7	chr1:217170600-217170800	Enhancers	Pancreas	Pancrea
8	chr1:217170600-217170800	Enhancers	Psoas Muscle	Psoas
9	chr1:217170600-217171400	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr1:217170600-217171600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr1:217170600-217171800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr1:217170600-217172000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr1:217170600-217172000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr1:217170800-217171000	Weak transcription	Pancreas	Pancrea
15	chr1:217170800-217171800	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr1:217170800-217173600	Weak transcription	Left Ventricle	heart
17	chr1:217171000-217171400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr1:217171000-217172000	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr1:217171400-217171600	Enhancers	Fetal Heart	heart
20	chr1:217173600-217174200	Enhancers	Left Ventricle	heart
21	chr1:217173600-217187600	Weak transcription	Fetal Heart	heart
22	chr1:217174200-217175200	Weak transcription	Left Ventricle	heart
23	chr1:217174600-217175200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr1:217176000-217176200	Enhancers	Left Ventricle	heart
25	chr1:217176000-217176200	Enhancers	Pancreas	Pancrea
26	chr1:217177800-217178800	Enhancers	Fetal Intestine Large	intestine
27	chr1:217178200-217179000	Enhancers	Fetal Intestine Small	intestine
28	chr1:217178800-217180000	Weak transcription	Fetal Intestine Large	intestine
29	chr1:217179000-217180400	Weak transcription	Fetal Intestine Small	intestine
30	chr1:217180000-217180800	Enhancers	Fetal Intestine Large	intestine
31	chr1:217180400-217180600	Enhancers	Fetal Intestine Small	intestine
32	chr1:217181800-217183800	Enhancers	Brain Substantia Nigra	brain
33	chr1:217182000-217182800	Enhancers	Brain Hippocampus Middle	brain
34	chr1:217182200-217182600	Enhancers	Brain Anterior Caudate	brain
35	chr1:217182200-217182800	Enhancers	Brain Angular Gyrus	brain
36	chr1:217182200-217183800	Enhancers	Brain Cingulate Gyrus	brain
37	chr1:217182400-217182600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:217182600-217182800	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr1:217182600-217182800	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr1:217182600-217182800	Enhancers	HMEC	breast
41	chr1:217182600-217183400	Weak transcription	Brain Anterior Caudate	brain
42	chr1:217182600-217183600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:217182600-217184200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr1:217182800-217183200	Weak transcription	Brain Angular Gyrus	brain
45	chr1:217182800-217184000	Weak transcription	Brain Hippocampus Middle	brain
46	chr1:217182800-217185800	Weak transcription	HMEC	breast
47	chr1:217183200-217183600	Enhancers	Brain Angular Gyrus	brain
48	chr1:217183400-217183600	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr1:217183400-217184200	Enhancers	Brain Anterior Caudate	brain
50	chr1:217183600-217184000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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