Variant report

Variant	esv3381703
Chromosome Location	chr2:114794745-114989429
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	chr2:114959467-114959735	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:114837190-114837497	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:114927789-114927905	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:114917857-114918324	HepG2	liver:	n/a	n/a
5	ATF3	chr2:114897230-114897385	K562	blood:	n/a	n/a
6	BATF	chr2:114841331-114841674	GM12878	blood:	n/a	n/a
7	BATF	chr2:114841354-114841562	GM12878	blood:	n/a	n/a
8	BATF	chr2:114813929-114814265	GM12878	blood:	n/a	n/a
9	BATF	chr2:114813848-114814248	GM12878	blood:	n/a	n/a
10	BATF	chr2:114841795-114842671	GM12878	blood:	n/a	n/a
11	BCL11A	chr2:114841340-114841570	GM12878	blood:	n/a	chr2:114841511-114841520 chr2:114841512-114841521
12	BCL11A	chr2:114813887-114814202	GM12878	blood:	n/a	chr2:114814024-114814033
13	BCL3	chr2:114813851-114814184	GM12878	blood:	n/a	chr2:114814024-114814033
14	BCL3	chr2:114841380-114841696	GM12878	blood:	n/a	chr2:114841511-114841520 chr2:114841512-114841521
15	BHLHE40	chr2:114807514-114807703	K562	blood:	n/a	n/a
16	BHLHE40	chr2:114897179-114897370	K562	blood:	n/a	n/a
17	BHLHE40	chr2:114807515-114807786	HepG2	liver:	n/a	n/a
18	BHLHE40	chr2:114841452-114841636	GM12878	blood:	n/a	n/a
19	BHLHE40	chr2:114880556-114880795	K562	blood:	n/a	n/a
20	CBX3	chr2:114949974-114950352	HCT-116	colon:	n/a	n/a
21	CEBPB	chr2:114917859-114918253	HepG2	liver:	n/a	chr2:114918051-114918062
22	CEBPB	chr2:114951205-114951440	A549	lung:	n/a	chr2:114951316-114951328 chr2:114951316-114951329 chr2:114951344-114951355 chr2:114951344-114951357
23	CEBPB	chr2:114874200-114874489	A549	lung:	n/a	chr2:114874330-114874341
24	CEBPB	chr2:114917912-114918112	K562	blood:	n/a	chr2:114918051-114918062
25	CEBPB	chr2:114874294-114874461	K562	blood:	n/a	chr2:114874330-114874341
26	CEBPB	chr2:114895878-114896129	IMR90	lung:	n/a	chr2:114895977-114895990 chr2:114895977-114895988 chr2:114895977-114895990
27	CEBPB	chr2:114949960-114950241	HepG2	liver:	n/a	chr2:114950074-114950085
28	CEBPB	chr2:114949967-114950247	Hela-S3	cervix:	n/a	chr2:114950074-114950085
29	CEBPB	chr2:114917921-114918178	IMR90	lung:	n/a	chr2:114918051-114918062
30	CEBPB	chr2:114927557-114928038	HepG2	liver:	n/a	chr2:114927726-114927737 chr2:114927728-114927739 chr2:114927728-114927737
31	CEBPB	chr2:114951166-114951478	HepG2	liver:	n/a	chr2:114951316-114951328 chr2:114951316-114951329 chr2:114951344-114951355 chr2:114951344-114951357
32	CEBPB	chr2:114917894-114918180	HepG2	liver:	n/a	chr2:114918051-114918062
33	CEBPB	chr2:114917860-114918254	HepG2	liver:	n/a	chr2:114918051-114918062
34	CEBPB	chr2:114980434-114980478	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr2:114883422-114883607	A549	lung:	n/a	chr2:114883459-114883476 chr2:114883525-114883536
36	CEBPB	chr2:114874246-114874460	H1-hESC	embryonic stem cell:	n/a	chr2:114874330-114874341
37	CEBPB	chr2:114917832-114918249	HepG2	liver:	n/a	chr2:114918051-114918062
38	CEBPB	chr2:114917940-114918252	MCF-7	breast:	n/a	chr2:114918051-114918062
39	CEBPB	chr2:114883450-114883645	HepG2	liver:	n/a	chr2:114883459-114883476 chr2:114883525-114883536
40	CEBPB	chr2:114848445-114848494	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr2:114949956-114950181	IMR90	lung:	n/a	chr2:114950074-114950085
42	CEBPB	chr2:114866128-114866302	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr2:114874198-114874548	HepG2	liver:	n/a	chr2:114874483-114874496 chr2:114874330-114874341 chr2:114874483-114874494 chr2:114874485-114874494
44	CEBPB	chr2:114927599-114927923	A549	lung:	n/a	chr2:114927726-114927737 chr2:114927728-114927739 chr2:114927728-114927737
45	CEBPB	chr2:114837022-114837598	HepG2	liver:	n/a	chr2:114837232-114837243 chr2:114837232-114837243
46	CEBPB	chr2:114980357-114980550	HepG2	liver:	n/a	n/a
47	CEBPB	chr2:114830378-114830482	HepG2	liver:	n/a	n/a
48	CEBPB	chr2:114874259-114874532	IMR90	lung:	n/a	chr2:114874483-114874496 chr2:114874330-114874341 chr2:114874483-114874494 chr2:114874485-114874494
49	CEBPB	chr2:114823358-114823519	HepG2	liver:	n/a	n/a
50	CEBPB	chr2:114895852-114896138	HepG2	liver:	n/a	chr2:114895977-114895990 chr2:114895977-114895988 chr2:114895977-114895990

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:114880656-114880706	AG10803	skin:	n/a
2	chr2:114866027-114866077	GM12891	blood:	n/a
3	chr2:114866027-114866077	HCPEpiC	choroid plexus:	n/a
4	chr2:114880656-114880706	SK-N-MC	brain:	n/a
5	chr2:114866027-114866077	PFSK-1	brain:	n/a
6	chr2:114880656-114880706	MCF-7	breast:	n/a
7	chr2:114866027-114866077	AG09309	skin:	n/a
8	chr2:114880656-114880706	HUVEC	blood vessel:	n/a
9	chr2:114880656-114880706	GM19239	blood:	n/a
10	chr2:114880656-114880706	GM12892	blood:	n/a
11	chr2:114866027-114866077	ProgFib	skin:	n/a
12	chr2:114880656-114880706	HCF	heart:	n/a
13	chr2:114880656-114880706	T-47D	breast:	n/a
14	chr2:114880656-114880706	SAEC	small airway:	n/a
15	chr2:114866027-114866077	HPAEpiC	pulmonary alveolar:	n/a
16	chr2:114880656-114880706	HepG2	liver:	n/a
17	chr2:114866027-114866077	A549	lung:	n/a
18	chr2:114880656-114880706	HNPCEpiC	eye:	n/a
19	chr2:114880656-114880706	HL-60	blood:	n/a
20	chr2:114880656-114880706	HIPEpiC	eye:	n/a
21	chr2:114866027-114866077	U87	brain:	n/a
22	chr2:114866027-114866077	MCF-7	breast:	n/a
23	chr2:114880656-114880706	HEEpiC	esophagus:	n/a
24	chr2:114880656-114880706	AG09309	skin:	n/a
25	chr2:114880656-114880706	H1-hESC	embryonic stem cell:	embryo
26	chr2:114880656-114880706	Jurkat	blood:	n/a
27	chr2:114866027-114866077	H1-hESC	embryonic stem cell:	embryo
28	chr2:114866027-114866077	T-47D	breast:	n/a
29	chr2:114880656-114880706	NT2-D1	testis:	n/a
30	chr2:114866027-114866077	HNPCEpiC	eye:	n/a
31	chr2:114880656-114880706	HCT-116	colon:	n/a
32	chr2:114866027-114866077	HCF	heart:	n/a
33	chr2:114880656-114880706	ECC-1	luminal epithelium:	n/a
34	chr2:114866027-114866077	Caco-2	colon:	n/a
35	chr2:114880656-114880706	ovcar-3	ovarian:	n/a
36	chr2:114866027-114866077	HL-60	blood:	n/a
37	chr2:114866027-114866077	HRPEpiC	eye:	n/a
38	chr2:114880656-114880706	ProgFib	skin:	n/a
39	chr2:114880656-114880706	PFSK-1	brain:	n/a
40	chr2:114880656-114880706	NHBE	bronchial:	n/a
41	chr2:114866027-114866077	NHDF-neo	bronchial:	n/a
42	chr2:114880656-114880706	HRCEpiC	kidney:	n/a
43	chr2:114866027-114866077	AG04450	lung:	fetal
44	chr2:114866027-114866077	GM06990	blood:	n/a
45	chr2:114866027-114866077	K562	blood:	n/a
46	chr2:114880656-114880706	Hela-S3	cervix:	n/a
47	chr2:114880656-114880706	AG04450	lung:	fetal
48	chr2:114866027-114866077	HepG2	liver:	n/a
49	chr2:114866027-114866077	NB4	blood:	n/a
50	chr2:114866027-114866077	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:114926346..114927947-chr2:114929131..114931475,2	K562	blood:
2	chr2:114825429..114827608-chr2:114831358..114833425,2	K562	blood:
3	chr2:114834506..114837502-chr2:114837788..114839706,2	K562	blood:
4	chr2:114834506..114837502-chr2:114837788..114839706,2	K562	blood:
5	chr2:114898363..114900991-chr2:114928789..114930816,2	K562	blood:
6	chr2:114898363..114900991-chr2:114928789..114930816,2	K562	blood:
7	chr2:114887346..114889259-chr2:114891013..114893015,2	K562	blood:
8	chr2:114735196..114736318-chr2:114959110..114959760,3	MCF-7	breast:
9	chr2:114827245..114829875-chr2:114832597..114835524,2	MCF-7	breast:
10	chr2:114827245..114829875-chr2:114832597..114835524,2	MCF-7	breast:
11	chr2:114939549..114941920-chr2:114942600..114945174,2	MCF-7	breast:
12	chr2:114926346..114927947-chr2:114929131..114931475,2	K562	blood:
13	chr2:114845247..114848431-chr2:114848488..114851616,3	K562	blood:
14	chr2:114845247..114848431-chr2:114848488..114851616,3	K562	blood:
15	chr2:114825429..114827608-chr2:114831358..114833425,2	K562	blood:
16	chr2:114887346..114889259-chr2:114891013..114893015,2	K562	blood:
17	chr2:114939549..114941920-chr2:114942600..114945174,2	MCF-7	breast:
18	chr1:242680127..242681627-chr2:114917951..114919998,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC35F5-6	chr2:114880595-114880870	XLOC_002288
2	lnc-SLC35F5-6	chr2:114879851-114880039	XLOC_002288

Variant related genes	Relation type
ENSG00000235242	TF binding region
ENSG00000235242	CpG island

Extended variants
information (count: 2997 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2997 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs156725	chr2:114794780-114794781	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532620392	chr2:114794811-114794812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184887966	chr2:114794819-114794820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs117662603	chr2:114794895-114794896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535045062	chr2:114794906-114794907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556941961	chr2:114794916-114794917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555140490	chr2:114794922-114794923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548871214	chr2:114794943-114794944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568366609	chr2:114794954-114794955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536669019	chr2:114794974-114794975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569559968	chr2:114794984-114794985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190815513	chr2:114794992-114794993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576563511	chr2:114795026-114795027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182128361	chr2:114795068-114795069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552939733	chr2:114795076-114795077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185909360	chr2:114795096-114795097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536783726	chr2:114795099-114795100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116430859	chr2:114795108-114795109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34249933	chr2:114795127-114795128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374329233	chr2:114795216-114795217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541621914	chr2:114795253-114795254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76834739	chr2:114795256-114795257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189223518	chr2:114795275-114795276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs13017953	chr2:114795281-114795282	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs563660122	chr2:114795291-114795292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73955484	chr2:114795309-114795310	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs552628265	chr2:114795348-114795349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs141923489	chr2:114795350-114795351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528686986	chr2:114795366-114795367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548464215	chr2:114795367-114795368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572248988	chr2:114795450-114795451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181175054	chr2:114795467-114795468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111319547	chr2:114795476-114795477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550188649	chr2:114795565-114795566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570109432	chr2:114795589-114795590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185705	chr2:114795592-114795593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546346351	chr2:114795608-114795609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539199553	chr2:114795639-114795640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553042799	chr2:114795640-114795641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564288021	chr2:114795657-114795658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1386294	chr2:114795670-114795671	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs182159	chr2:114795671-114795672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185583346	chr2:114795690-114795691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs172116	chr2:114795712-114795713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555569188	chr2:114795722-114795723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192463	chr2:114795751-114795752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs419396	chr2:114795771-114795772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs56742178	chr2:114795808-114795809	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs544499403	chr2:114795830-114795831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558041760	chr2:114795858-114795859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:114790800-114798400	Weak transcription	Fetal Brain Male	brain
2	chr2:114797200-114799400	Enhancers	Fetal Brain Female	brain
3	chr2:114798400-114798800	Enhancers	Pancreas	Pancrea
4	chr2:114798400-114799200	Enhancers	Fetal Brain Male	brain
5	chr2:114799200-114804000	Weak transcription	Fetal Brain Male	brain
6	chr2:114804000-114805600	Enhancers	Fetal Brain Male	brain
7	chr2:114806400-114808000	Enhancers	HMEC	breast
8	chr2:114806400-114808200	Enhancers	NHEK	skin
9	chr2:114806800-114807800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr2:114806800-114808000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr2:114813600-114814200	Enhancers	GM12878-XiMat	blood
12	chr2:114813800-114814000	Enhancers	Rectal Mucosa Donor 29	rectum
13	chr2:114813800-114815200	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr2:114814000-114814200	Enhancers	Sigmoid Colon	Sigmoid Colon
15	chr2:114814200-114815200	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr2:114815200-114815600	Active TSS	Rectal Mucosa Donor 31	rectum
17	chr2:114815200-114816000	Active TSS	Rectal Mucosa Donor 29	rectum
18	chr2:114815200-114816000	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr2:114815600-114816000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
20	chr2:114820400-114821000	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr2:114820400-114821600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr2:114820600-114821000	Enhancers	H9 Cell Line	embryonic stem cell
23	chr2:114820600-114821000	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr2:114820600-114821000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:114820600-114821400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr2:114820800-114821200	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr2:114820800-114821800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr2:114820800-114822000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr2:114823400-114824000	Enhancers	Liver	Liver
30	chr2:114823400-114824200	Enhancers	Pancreas	Pancrea
31	chr2:114823600-114823800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr2:114823600-114823800	Bivalent Enhancer	HepG2	liver
33	chr2:114833600-114835000	Enhancers	Liver	Liver
34	chr2:114834000-114834600	Bivalent Enhancer	HepG2	liver
35	chr2:114834600-114835000	Flanking Bivalent TSS/Enh	HepG2	liver
36	chr2:114835000-114835200	Bivalent Enhancer	HepG2	liver
37	chr2:114835000-114836600	Weak transcription	Liver	Liver
38	chr2:114835400-114836600	Weak transcription	HepG2	liver
39	chr2:114836600-114837000	Enhancers	HepG2	liver
40	chr2:114836600-114837200	Enhancers	Liver	Liver
41	chr2:114837000-114837400	Flanking Active TSS	HepG2	liver
42	chr2:114837400-114838000	Enhancers	HepG2	liver
43	chr2:114837600-114838000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:114838000-114839000	Weak transcription	HepG2	liver
45	chr2:114839000-114839400	ZNF genes & repeats	HepG2	liver
46	chr2:114839400-114840200	Weak transcription	HepG2	liver
47	chr2:114840200-114840400	Enhancers	HepG2	liver
48	chr2:114840200-114840800	Enhancers	Brain Substantia Nigra	brain
49	chr2:114840400-114840800	Enhancers	Brain Angular Gyrus	brain
50	chr2:114840400-114840800	Enhancers	Brain Hippocampus Middle	brain

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