Variant report

Variant	nsv573358
Chromosome Location	chr16:81232426-81240697
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	chr16:81238280-81238430	HVMF	connective:	n/a	n/a
8	CTCF	chr16:81238703-81239008	GM13977	blood:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
9	CTCF	chr16:81238725-81238963	GM12892	blood:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
10	CTCF	chr16:81238800-81238950	HUVEC	blood vessel:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
11	CTCF	chr16:81232378-81232565	Fibrobl	skin:	n/a	n/a
12	CTCF	chr16:81238780-81238930	HRE	kidney:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
13	CTCF	chr16:81238780-81238930	HEEpiC	esophagus:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
14	CTCF	chr16:81238780-81238930	GM12867	blood:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
15	CTCF	chr16:81238460-81238610	HCT-116	colon:	n/a	n/a
16	CTCF	chr16:81232380-81232530	AG09319	gingival:	n/a	n/a
17	CTCF	chr16:81238800-81238950	RPTEC	kidney:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
18	CTCF	chr16:81238800-81238950	HEEpiC	esophagus:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
19	CTCF	chr16:81238671-81239000	K562	blood:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
20	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
21	CTCF	chr16:81238780-81238930	HCPEpiC	choroid plexus:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
22	CTCF	chr16:81238700-81238850	HFF	foreskin:	n/a	n/a
23	CTCF	chr16:81238840-81238990	SAEC	small airway:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
24	CTCF	chr16:81238498-81238612	GM19240	blood:	n/a	n/a
25	CTCF	chr16:81238671-81239009	A549	lung:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
26	CTCF	chr16:81238752-81238931	GM12891	blood:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
27	CTCF	chr16:81238721-81238960	GM19239	blood:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
28	CTCF	chr16:81238739-81238982	GM10266	blood:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
29	CTCF	chr16:81238717-81238970	HepG2	liver:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
30	CTCF	chr16:81232400-81232550	NHEK	skin:	n/a	n/a
31	CTCF	chr16:81232360-81232510	GM12864	blood:	n/a	n/a
32	CTCF	chr16:81232400-81232550	MCF-7	breast:	n/a	n/a
33	CTCF	chr16:81232419-81232514	GM20000	blood:	n/a	n/a
34	CTCF	chr16:81232360-81232510	HepG2	liver:	n/a	n/a
35	CTCF	chr16:81238780-81238930	AoAF	blood vessel:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
36	CTCF	chr16:81238780-81238930	HA-sp	spinal cord:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
37	CTCF	chr16:81238800-81238950	HCPEpiC	choroid plexus:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
38	CTCF	chr16:81232440-81232590	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr16:81232360-81232510	AG10803	skin:	n/a	n/a
40	CTCF	chr16:81238716-81239005	Spleen_OC	spleen:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
41	CTCF	chr16:81232308-81232552	A549	lung:	n/a	n/a
42	CTCF	chr16:81232377-81232552	GM12892	blood:	n/a	n/a
43	CTCF	chr16:81232400-81232550	HMEC	breast:	n/a	n/a
44	CTCF	chr16:81238780-81238930	AG09319	gingival:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
45	CTCF	chr16:81239200-81239350	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr16:81238740-81238890	GM12869	blood:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
47	CTCF	chr16:81238735-81238984	Pancreas_OC	pancreas:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
48	CTCF	chr16:81238396-81239306	A549	lung:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
49	CTCF	chr16:81238780-81238930	K562	blood:	n/a	chr16:81238854-81238867 chr16:81238854-81238867 chr16:81238852-81238868 chr16:81238851-81238869 chr16:81238853-81238874
50	CTCF	chr16:81232380-81232530	HCPEpiC	choroid plexus:	n/a	n/a

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

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

Extended variants
information (count: 593 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:593 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9934856	chr16:81232426-81232427	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs373285026	chr16:81232429-81232430	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs111719039	chr16:81232479-81232480	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs9934872	chr16:81232484-81232485	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs9937071	chr16:81232490-81232491	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs201929151	chr16:81232494-81232495	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs200035205	chr16:81232502-81232503	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs138937023	chr16:81232539-81232540	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs562980257	chr16:81232540-81232541	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs370776690	chr16:81232553-81232554	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs149011789	chr16:81232554-81232555	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs7194871	chr16:81232564-81232565	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs76852683	chr16:81232567-81232568	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs374297288	chr16:81232577-81232578	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs201901170	chr16:81232582-81232583	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs9937169	chr16:81232590-81232591	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs371508103	chr16:81232595-81232596	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs374451549	chr16:81232596-81232597	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs572713132	chr16:81232597-81232598	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs147081720	chr16:81232601-81232602	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs371845680	chr16:81232602-81232603	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs200535438	chr16:81232614-81232615	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs367962541	chr16:81232622-81232623	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs527848230	chr16:81232624-81232625	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs138475973	chr16:81232625-81232626	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs184785676	chr16:81232637-81232638	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs199866986	chr16:81232656-81232657	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs564971777	chr16:81232665-81232666	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs200496228	chr16:81232676-81232677	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs536775467	chr16:81232708-81232709	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs377189634	chr16:81232717-81232718	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs532200619	chr16:81232740-81232741	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs9924038	chr16:81232743-81232744	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs80107742	chr16:81232767-81232768	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs536571173	chr16:81232770-81232771	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs538582900	chr16:81232840-81232841	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs367923126	chr16:81232900-81232901	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs188382083	chr16:81232901-81232902	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs147269480	chr16:81232906-81232907	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs537840310	chr16:81232907-81232908	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs556091003	chr16:81232921-81232922	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs577723349	chr16:81232956-81232957	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs193026206	chr16:81232963-81232964	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs184934662	chr16:81232973-81232974	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs541830612	chr16:81233026-81233027	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs572523677	chr16:81233028-81233029	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs543336651	chr16:81233040-81233041	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs148336739	chr16:81233068-81233069	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs576156343	chr16:81233089-81233090	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs189827399	chr16:81233104-81233105	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:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81215000-81254600	Weak transcription	Right Atrium	heart
2	chr16:81229800-81238600	Weak transcription	Adipose Nuclei	Adipose
3	chr16:81230600-81238400	Weak transcription	Brain Anterior Caudate	brain
4	chr16:81232000-81232800	Enhancers	Brain Hippocampus Middle	brain
5	chr16:81232200-81232600	Active TSS	Brain Substantia Nigra	brain
6	chr16:81232400-81232600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr16:81232400-81232600	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr16:81232400-81232800	Enhancers	Liver	Liver
9	chr16:81232400-81232800	Bivalent Enhancer	HepG2	liver
10	chr16:81232400-81234800	Weak transcription	Brain Cingulate Gyrus	brain
11	chr16:81232400-81238600	Weak transcription	Brain Angular Gyrus	brain
12	chr16:81232600-81234800	Weak transcription	Brain Substantia Nigra	brain
13	chr16:81232600-81238400	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr16:81232800-81234800	Weak transcription	Liver	Liver
15	chr16:81232800-81238600	Weak transcription	Brain Hippocampus Middle	brain
16	chr16:81234800-81235200	Enhancers	Brain Cingulate Gyrus	brain
17	chr16:81234800-81235200	Enhancers	Brain Substantia Nigra	brain
18	chr16:81234800-81235400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr16:81234800-81235400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr16:81234800-81235400	Enhancers	Liver	Liver
21	chr16:81235000-81235200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
22	chr16:81235000-81235400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr16:81235200-81238400	Weak transcription	Brain Cingulate Gyrus	brain
24	chr16:81235200-81238400	Weak transcription	Brain Substantia Nigra	brain
25	chr16:81235400-81238400	Weak transcription	Liver	Liver
26	chr16:81237000-81237400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr16:81237000-81237600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr16:81238000-81238400	Enhancers	Placenta	Placenta
29	chr16:81238400-81239000	Enhancers	Liver	Liver
30	chr16:81238400-81239200	Enhancers	Brain Anterior Caudate	brain
31	chr16:81238400-81239200	Enhancers	Brain Cingulate Gyrus	brain
32	chr16:81238400-81239200	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr16:81238400-81239200	Enhancers	Brain Substantia Nigra	brain
34	chr16:81238600-81238800	Flanking Active TSS	Colon Smooth Muscle	Colon
35	chr16:81238600-81239200	Enhancers	Adipose Nuclei	Adipose
36	chr16:81238600-81239200	Enhancers	Brain Angular Gyrus	brain
37	chr16:81238600-81239200	Enhancers	Rectal Smooth Muscle	rectum
38	chr16:81238600-81239400	Enhancers	Brain Hippocampus Middle	brain
39	chr16:81238800-81239400	Enhancers	Colon Smooth Muscle	Colon
40	chr16:81240600-81241200	Enhancers	Fetal Lung	lung

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