Variant report

Variant	nsv573356
Chromosome Location	chr16:81230341-81240644
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	chr16:81238678-81239059	K562	blood:	n/a	n/a
2	ARID3A	chr16:81232328-81232582	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:81238745-81239052	HepG2	liver:	n/a	n/a
4	BHLHE40	chr16:81238713-81238961	K562	blood:	n/a	n/a
5	BRCA1	chr16:81232353-81232533	HepG2	liver:	n/a	n/a
6	CEBPB	chr16:81240004-81240129	HepG2	liver:	n/a	n/a
7	CTCF	chr16:81238720-81238870	WERI-Rb-1	eye:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869
8	CTCF	chr16:81232360-81232510	HUVEC	blood vessel:	n/a	n/a
9	CTCF	chr16:81232340-81232490	HEEpiC	esophagus:	n/a	n/a
10	CTCF	chr16:81238800-81238950	HCM	heart:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
11	CTCF	chr16:81232400-81232550	GM12871	blood:	n/a	n/a
12	CTCF	chr16:81238640-81239140	MCF-7	breast:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
13	CTCF	chr16:81238749-81238969	GM20000	blood:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
14	CTCF	chr16:81232360-81232510	K562	blood:	n/a	n/a
15	CTCF	chr16:81232320-81232470	WI-38	lung:	n/a	n/a
16	CTCF	chr16:81232420-81232570	NHDF-neo	bronchial:	n/a	n/a
17	CTCF	chr16:81238609-81239107	K562	blood:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
18	CTCF	chr16:81238800-81238950	NHEK	skin:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
19	CTCF	chr16:81238800-81238950	BE2_C	brain:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
20	CTCF	chr16:81238752-81238931	GM12891	blood:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
21	CTCF	chr16:81238703-81239030	Medullo	brain:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
22	CTCF	chr16:81238280-81238430	HVMF	connective:	n/a	n/a
23	CTCF	chr16:81238629-81239080	K562	blood:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
24	CTCF	chr16:81238800-81238950	HAc	cerebellar:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
25	CTCF	chr16:81232317-81232639	T-47D	breast:	n/a	n/a
26	CTCF	chr16:81232380-81232530	HVMF	connective:	n/a	n/a
27	CTCF	chr16:81232380-81232530	HMF	breast:	n/a	n/a
28	CTCF	chr16:81232400-81232550	HCM	heart:	n/a	n/a
29	CTCF	chr16:81232343-81232605	MCF-7	breast:	n/a	n/a
30	CTCF	chr16:81238800-81238950	AG09319	gingival:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
31	CTCF	chr16:81238614-81239036	K562	blood:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
32	CTCF	chr16:81238780-81238930	Caco-2	colon:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
33	CTCF	chr16:81238780-81238930	AG04449	skin:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
34	CTCF	chr16:81238760-81238910	GM06990	blood:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
35	CTCF	chr16:81232368-81232576	NHEK	skin:	n/a	n/a
36	CTCF	chr16:81232292-81232609	HepG2	liver:	n/a	n/a
37	CTCF	chr16:81238671-81238990	ECC-1	luminal epithelium:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
38	CTCF	chr16:81238840-81238990	BJ	skin:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
39	CTCF	chr16:81232400-81232550	NHLF	lung:	n/a	n/a
40	CTCF	chr16:81232400-81232550	NB4	blood:	n/a	n/a
41	CTCF	chr16:81238739-81238982	GM10266	blood:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
42	CTCF	chr16:81238716-81239005	Spleen_OC	spleen:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
43	CTCF	chr16:81238780-81238930	AG09309	skin:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
44	CTCF	chr16:81238800-81238950	NHDF-neo	bronchial:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
45	CTCF	chr16:81238780-81238930	GM12867	blood:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
46	CTCF	chr16:81232380-81232530	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr16:81238740-81238890	HEK293	kidney:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
48	CTCF	chr16:81232236-81232699	HepG2	liver:	n/a	n/a
49	CTCF	chr16:81232354-81232516	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr16:81238689-81239069	T-47D	breast:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874

No.	Distal block	Cell Line	Cell type
1	chr16:81129494..81132038-chr16:81235972..81238926,2	MCF-7	breast:
2	chr16:81068494..81071039-chr16:81229020..81231792,3	MCF-7	breast:
3	chr16:81237375..81239298-chr16:81246693..81248653,2	K562	blood:
4	chr16:81238408..81239122-chr16:81294572..81295294,2	K562	blood:
5	chr16:81232049..81234951-chr16:81236497..81238711,3	MCF-7	breast:
6	chr16:81221033..81223620-chr16:81234908..81237258,2	K562	blood:
7	chr16:81110779..81112641-chr16:81230562..81234042,3	MCF-7	breast:
8	chr16:81068964..81069731-chr16:81231614..81232947,4	MCF-7	breast:
9	chr12:127828951..127829931-chr16:81238548..81239098,2	MCF-7	breast:
10	chr16:81230952..81233745-chr16:81235442..81237465,2	MCF-7	breast:
11	chr16:81068894..81069816-chr16:81231960..81232923,14	MCF-7	breast:
12	chr16:81174893..81175517-chr16:81231737..81232731,3	MCF-7	breast:
13	chr16:81069222..81069838-chr16:81238638..81239329,2	MCF-7	breast:
14	chr16:81069108..81070906-chr16:81231938..81234335,3	MCF-7	breast:
15	chr16:81110861..81112388-chr16:81235998..81238926,2	MCF-7	breast:
16	chr16:81238218..81239252-chr16:81247860..81248811,3	MCF-7	breast:
17	chr16:81238415..81238961-chr16:81294445..81295011,2	MCF-7	breast:
18	chr16:81238393..81239236-chr16:81383637..81384525,3	MCF-7	breast:
19	chr12:108895394..108895894-chr16:81238428..81239017,2	MCF-7	breast:
20	chr16:81238472..81239333-chr16:81771352..81772219,3	MCF-7	breast:

Variant related genes	Relation type
PKD1L2	TF binding region
ENSG00000261218	chromatin interactions
ENSG00000140905	chromatin interactions
ENSG00000260213	chromatin interactions
ENSG00000245059	chromatin interactions
ENSG00000166455	chromatin interactions
ENSG00000166454	chromatin interactions
ENSG00000166473	chromatin interactions

Extended variants
information (count: 746 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:746 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4076583	chr16:81230341-81230342	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186093270	chr16:81230352-81230353	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs577615571	chr16:81230365-81230366	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs75303368	chr16:81230379-81230380	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs34261179	chr16:81230381-81230382	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs11648160	chr16:81230408-81230409	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs541941631	chr16:81230431-81230432	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs4076584	chr16:81230444-81230445	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs35650845	chr16:81230445-81230446	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs190659237	chr16:81230491-81230492	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs563895243	chr16:81230492-81230493	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs147519997	chr16:81230514-81230515	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs77642334	chr16:81230521-81230522	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs566096822	chr16:81230567-81230568	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs576448897	chr16:81230578-81230579	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs530029415	chr16:81230581-81230582	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs182875313	chr16:81230605-81230606	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs570050630	chr16:81230614-81230615	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs537497257	chr16:81230646-81230647	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs28719864	chr16:81230651-81230652	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs548321667	chr16:81230658-81230659	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs187149888	chr16:81230670-81230671	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs553373863	chr16:81230713-81230714	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs574413436	chr16:81230735-81230736	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs541456347	chr16:81230736-81230737	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs191247150	chr16:81230750-81230751	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs183164783	chr16:81230769-81230770	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs187607367	chr16:81230780-81230781	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs563963793	chr16:81230831-81230832	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs528251865	chr16:81230853-81230854	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs192569267	chr16:81230858-81230859	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs561827870	chr16:81230861-81230862	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs530156759	chr16:81230868-81230869	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs548296736	chr16:81230870-81230871	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs185722807	chr16:81230923-81230924	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs143924224	chr16:81230924-81230925	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs187894568	chr16:81230927-81230928	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs571089204	chr16:81230956-81230957	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs535219483	chr16:81230968-81230969	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs547315925	chr16:81230990-81230991	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs568660385	chr16:81231000-81231001	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs192282348	chr16:81231003-81231004	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs573536237	chr16:81231006-81231007	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs11150365	chr16:81231011-81231012	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs565109614	chr16:81231025-81231026	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs112659996	chr16:81231034-81231035	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs539177143	chr16:81231037-81231038	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs11866388	chr16:81231043-81231044	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs184462739	chr16:81231048-81231049	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs112887439	chr16:81231049-81231050	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Neuroblastoma	18923524	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Obesity	20622171	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	21990379	CNVD

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81215000-81254600	Weak transcription	Right Atrium	heart
2	chr16:81218000-81230400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr16:81224600-81230400	Weak transcription	Brain Cingulate Gyrus	brain
4	chr16:81224600-81232000	Weak transcription	Brain Substantia Nigra	brain
5	chr16:81227000-81232000	Weak transcription	Liver	Liver
6	chr16:81229400-81230400	Bivalent Enhancer	Fetal Stomach	stomach
7	chr16:81229600-81230600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr16:81229800-81230600	Enhancers	Brain Hippocampus Middle	brain
9	chr16:81229800-81238600	Weak transcription	Adipose Nuclei	Adipose
10	chr16:81230200-81230600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
11	chr16:81230400-81230600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr16:81230400-81230800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr16:81230400-81230800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr16:81230400-81231000	Enhancers	Brain Cingulate Gyrus	brain
15	chr16:81230600-81230800	Enhancers	Brain Angular Gyrus	brain
16	chr16:81230600-81232000	Weak transcription	Brain Hippocampus Middle	brain
17	chr16:81230600-81238400	Weak transcription	Brain Anterior Caudate	brain
18	chr16:81230800-81232000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr16:81231000-81232000	Weak transcription	Brain Angular Gyrus	brain
20	chr16:81231000-81232000	Weak transcription	Brain Cingulate Gyrus	brain
21	chr16:81231800-81232000	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr16:81232000-81232200	Active TSS	Brain Angular Gyrus	brain
23	chr16:81232000-81232200	Flanking Active TSS	Brain Substantia Nigra	brain
24	chr16:81232000-81232200	Bivalent Enhancer	HepG2	liver
25	chr16:81232000-81232400	Flanking Active TSS	Liver	Liver
26	chr16:81232000-81232400	Active TSS	Brain Cingulate Gyrus	brain
27	chr16:81232000-81232400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
28	chr16:81232000-81232800	Enhancers	Brain Hippocampus Middle	brain
29	chr16:81232200-81232400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr16:81232200-81232400	Flanking Active TSS	Brain Angular Gyrus	brain
31	chr16:81232200-81232400	Flanking Bivalent TSS/Enh	HepG2	liver
32	chr16:81232200-81232600	Active TSS	Brain Substantia Nigra	brain
33	chr16:81232400-81232600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr16:81232400-81232600	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr16:81232400-81232800	Enhancers	Liver	Liver
36	chr16:81232400-81232800	Bivalent Enhancer	HepG2	liver
37	chr16:81232400-81234800	Weak transcription	Brain Cingulate Gyrus	brain
38	chr16:81232400-81238600	Weak transcription	Brain Angular Gyrus	brain
39	chr16:81232600-81234800	Weak transcription	Brain Substantia Nigra	brain
40	chr16:81232600-81238400	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr16:81232800-81234800	Weak transcription	Liver	Liver
42	chr16:81232800-81238600	Weak transcription	Brain Hippocampus Middle	brain
43	chr16:81234800-81235200	Enhancers	Brain Cingulate Gyrus	brain
44	chr16:81234800-81235200	Enhancers	Brain Substantia Nigra	brain
45	chr16:81234800-81235400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr16:81234800-81235400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr16:81234800-81235400	Enhancers	Liver	Liver
48	chr16:81235000-81235200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
49	chr16:81235000-81235400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr16:81235200-81238400	Weak transcription	Brain Cingulate Gyrus	brain

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