Variant report

Variant	nsv1005298
Chromosome Location	chr2:210277791-210318067
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:815)
CpG islands
(count:794)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:815 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:210290241-210290562	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:210288326-210288644	HepG2	liver:	n/a	n/a
3	ATF2	chr2:210291086-210291503	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr2:210291046-210291505	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr2:210288339-210288758	HepG2	liver:	n/a	n/a
6	ATF3	chr2:210288422-210288656	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr2:210288473-210288708	K562	blood:	n/a	n/a
8	ATF3	chr2:210288353-210288780	A549	lung:	n/a	n/a
9	BACH1	chr2:210315954-210316348	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr2:210288317-210289169	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:210291104-210291445	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr2:210303344-210303348	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr2:210288477-210288694	GM12878	blood:	n/a	chr2:210288645-210288661 chr2:210288572-210288588 chr2:210288511-210288527 chr2:210288566-210288582 chr2:210288569-210288585 chr2:210288519-210288535
14	BHLHE40	chr2:210288461-210288462	K562	blood:	n/a	n/a
15	BRCA1	chr2:210288477-210288670	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr2:210290117-210290128	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr2:210288508-210288622	HepG2	liver:	n/a	n/a
18	CBX3	chr2:210288430-210288710	K562	blood:	n/a	n/a
19	CCNT2	chr2:210288427-210288911	K562	blood:	n/a	n/a
20	CEBPB	chr2:210316192-210316427	A549	lung:	n/a	chr2:210316293-210316304
21	CEBPB	chr2:210290251-210290545	A549	lung:	n/a	chr2:210290406-210290419
22	CEBPB	chr2:210290141-210290630	A549	lung:	n/a	chr2:210290406-210290419
23	CEBPB	chr2:210288478-210288640	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr2:210290203-210290611	Hela-S3	cervix:	n/a	chr2:210290406-210290419
25	CEBPB	chr2:210295132-210295269	H1-hESC	embryonic stem cell:	n/a	chr2:210295177-210295188 chr2:210295176-210295187 chr2:210295176-210295189
26	CEBPB	chr2:210316134-210316499	ECC-1	luminal epithelium:	n/a	chr2:210316293-210316304
27	CEBPB	chr2:210291156-210291446	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr2:210294995-210295355	HepG2	liver:	n/a	chr2:210295177-210295188 chr2:210295176-210295187 chr2:210295176-210295189
29	CEBPB	chr2:210310055-210310326	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:210288439-210288745	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr2:210316133-210316420	HepG2	liver:	n/a	chr2:210316293-210316304
32	CEBPB	chr2:210295107-210295249	K562	blood:	n/a	chr2:210295177-210295188 chr2:210295176-210295187 chr2:210295176-210295189
33	CEBPB	chr2:210291148-210291415	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr2:210315996-210316607	H1-hESC	embryonic stem cell:	n/a	chr2:210316293-210316304
35	CHD2	chr2:210288391-210288906	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr2:210288453-210288638	K562	blood:	n/a	n/a
37	CHD2	chr2:210288171-210288733	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr2:210288415-210288784	HepG2	liver:	n/a	n/a
39	CREB1	chr2:210288381-210288846	A549	lung:	n/a	n/a
40	CREB1	chr2:210288465-210288670	A549	lung:	n/a	n/a
41	CTBP2	chr2:210288073-210289360	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTBP2	chr2:210315930-210316381	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr2:210290360-210290510	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr2:210290320-210290473	GM19239	blood:	n/a	n/a
45	CTCF	chr2:210290380-210290530	HAc	cerebellar:	n/a	n/a
46	CTCF	chr2:210288435-210288802	A549	lung:	n/a	chr2:210288750-210288763
47	CTCF	chr2:210288540-210288690	GM12867	blood:	n/a	n/a
48	CTCF	chr2:210288480-210288630	HRE	kidney:	n/a	n/a
49	CTCF	chr2:210288980-210289130	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr2:210289073-210289281	NHEK	skin:	n/a	chr2:210289198-210289211

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:210288764-210288814	AG04449	skin:	fetal
2	chr2:210288764-210288814	AG04449	skin:	fetal
3	chr2:210298155-210298205	AG10803	skin:	n/a
4	chr2:210288540-210288590	Jurkat	blood:	n/a
5	chr2:210288540-210288590	SAEC	small airway:	n/a
6	chr2:210288514-210288564	AG04450	lung:	fetal
7	chr2:210288244-210288294	IMR90	lung:	fetal
8	chr2:210298155-210298205	HCM	heart:	n/a
9	chr2:210292579-210292629	AG04450	lung:	fetal
10	chr2:210286628-210286678	NB4	blood:	n/a
11	chr2:210288540-210288590	Hela-S3	cervix:	n/a
12	chr2:210288540-210288590	HUVEC	blood vessel:	n/a
13	chr2:210288540-210288590	MCF-7	breast:	n/a
14	chr2:210289210-210289260	NHBE	bronchial:	n/a
15	chr2:210288540-210288590	NT2-D1	testis:	n/a
16	chr2:210288514-210288564	SK-N-SH	brain:	n/a
17	chr2:210289210-210289260	HCT-116	colon:	n/a
18	chr2:210288514-210288564	K562	blood:	n/a
19	chr2:210288514-210288564	HUVEC	blood vessel:	n/a
20	chr2:210288514-210288564	CMK	blood:	n/a
21	chr2:210289210-210289260	Jurkat	blood:	n/a
22	chr2:210290621-210290671	A549	lung:	n/a
23	chr2:210298155-210298205	A549	lung:	n/a
24	chr2:210286628-210286678	SK-N-SH_RA	brain:	n/a
25	chr2:210288764-210288814	RPTEC	kidney:	n/a
26	chr2:210286628-210286678	HCF	heart:	n/a
27	chr2:210286628-210286678	MCF-7	breast:	n/a
28	chr2:210288540-210288590	HRPEpiC	eye:	n/a
29	chr2:210298155-210298205	HPAEpiC	pulmonary alveolar:	n/a
30	chr2:210286628-210286678	AG10803	skin:	n/a
31	chr2:210288391-210288441	T-47D	breast:	n/a
32	chr2:210316331-210316381	MCF-7	breast:	n/a
33	chr2:210316331-210316381	Hela-S3	cervix:	n/a
34	chr2:210288967-210289017	ovcar-3	ovarian:	n/a
35	chr2:210316331-210316381	BJ	skin:	n/a
36	chr2:210298155-210298205	PrEC	prostate:	n/a
37	chr2:210288764-210288814	HRPEpiC	eye:	n/a
38	chr2:210316331-210316381	NHDF-neo	bronchial:	n/a
39	chr2:210288391-210288441	U87	brain:	n/a
40	chr2:210288764-210288814	AG09309	skin:	n/a
41	chr2:210288391-210288441	NHDF-neo	bronchial:	n/a
42	chr2:210288244-210288294	ProgFib	skin:	n/a
43	chr2:210288514-210288564	GM06990	blood:	n/a
44	chr2:210298155-210298205	NB4	blood:	n/a
45	chr2:210289210-210289260	AG09309	skin:	n/a
46	chr2:210286628-210286678	LNCaP	prostate:	n/a
47	chr2:210288764-210288814	U87	brain:	n/a
48	chr2:210289210-210289260	AG04449	skin:	fetal
49	chr2:210292579-210292629	BE2_C	brain:	n/a
50	chr2:210298155-210298205	SK-N-MC	brain:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:210304298..210306345-chr2:210309816..210311784,2	MCF-7	breast:
2	chr2:210289883..210290530-chr2:210420774..210421369,3	MCF-7	breast:
3	chr2:210287559..210290365-chr2:210315823..210318569,2	MCF-7	breast:
4	chr2:210299119..210301868-chr2:210304043..210306218,2	MCF-7	breast:
5	chr2:210290034..210290731-chr2:210441735..210442573,2	MCF-7	breast:
6	chr2:210313244..210314912-chr2:210314992..210317272,2	MCF-7	breast:
7	chr2:210288165..210288679-chr2:210308477..210309152,2	K562	blood:
8	chr2:210313244..210314912-chr2:210314992..210317272,2	MCF-7	breast:
9	chr2:210304298..210306345-chr2:210309816..210311784,2	MCF-7	breast:
10	chr2:210291185..210292983-chr2:210295300..210297710,2	MCF-7	breast:
11	chr2:210299119..210301868-chr2:210304043..210306218,2	MCF-7	breast:
12	chr10:76995464..76995985-chr2:210288500..210289030,2	MCF-7	breast:
13	chr2:210288971..210290856-chr2:210420793..210422129,13	MCF-7	breast:
14	chr2:210291185..210292983-chr2:210295300..210297710,2	MCF-7	breast:
15	chr2:210288753..210291116-chr2:210291474..210294355,2	K562	blood:
16	chr2:210288165..210288679-chr2:210308477..210309152,2	K562	blood:
17	chr2:210281736..210283390-chr2:210288696..210290442,2	MCF-7	breast:

No data

Variant related genes	Relation type
MAP2	TF binding region
MAP2	CpG island
ENSG00000078018	chromatin interactions
ENSG00000165644	chromatin interactions

Extended variants
information (count: 1342 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1342 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141697984	chr2:210277873-210277874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs147133026	chr2:210277912-210277913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs77227796	chr2:210277942-210277943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs73065154	chr2:210277958-210277959	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs111398433	chr2:210277989-210277990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574227817	chr2:210277995-210277996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543155446	chr2:210278012-210278013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375528507	chr2:210278018-210278019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138676831	chr2:210278027-210278028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs142849332	chr2:210278045-210278046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545651080	chr2:210278070-210278071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565477188	chr2:210278116-210278117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530405601	chr2:210278123-210278124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs117162400	chr2:210278125-210278126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560638489	chr2:210278136-210278137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529698194	chr2:210278212-210278213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs9679620	chr2:210278362-210278363	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs566629797	chr2:210278374-210278375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538470701	chr2:210278384-210278385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188771636	chr2:210278395-210278396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs372067624	chr2:210278412-210278413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs35793696	chr2:210278437-210278438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533654219	chr2:210278453-210278454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs76236419	chr2:210278454-210278455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569201020	chr2:210278470-210278471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs13393446	chr2:210278492-210278493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181587484	chr2:210278503-210278504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185351024	chr2:210278563-210278564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574087484	chr2:210278566-210278567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs55883327	chr2:210278597-210278598	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs9677799	chr2:210278658-210278659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553207560	chr2:210278672-210278673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147431930	chr2:210278695-210278696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545303096	chr2:210278701-210278702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs372991022	chr2:210278722-210278723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs188654782	chr2:210278756-210278757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs535201721	chr2:210278757-210278758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs75345704	chr2:210278767-210278768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544510463	chr2:210278768-210278769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs369254392	chr2:210278842-210278843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs180803602	chr2:210278845-210278846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546637301	chr2:210278864-210278865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186248537	chr2:210278879-210278880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375722194	chr2:210278932-210278933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551616345	chr2:210278942-210278943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532312045	chr2:210279066-210279067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552132627	chr2:210279079-210279080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569084119	chr2:210279154-210279155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139224699	chr2:210279215-210279216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548526071	chr2:210279421-210279422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	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
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Mantle cell lymphoma	21518781	CNVD

Chromatin state (count:729 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:210275600-210280400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:210276800-210287200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:210277800-210278800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr2:210277800-210278800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr2:210278000-210278600	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr2:210279000-210288400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr2:210280400-210280800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr2:210283600-210284000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr2:210284200-210284800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr2:210285200-210285400	ZNF genes & repeats	Psoas Muscle	Psoas
11	chr2:210285400-210288200	Weak transcription	Psoas Muscle	Psoas
12	chr2:210286800-210288200	Enhancers	NHEK	skin
13	chr2:210287000-210287200	Enhancers	Pancreas	Pancrea
14	chr2:210287000-210288000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr2:210287200-210287400	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr2:210287200-210287400	Enhancers	Esophagus	oesophagus
17	chr2:210287200-210288200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr2:210287200-210288200	Weak transcription	Pancreas	Pancrea
19	chr2:210287200-210288200	Enhancers	HMEC	breast
20	chr2:210287200-210288400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr2:210287400-210287600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr2:210287400-210288000	Weak transcription	Esophagus	oesophagus
23	chr2:210287800-210288000	Enhancers	Brain Anterior Caudate	brain
24	chr2:210287800-210288000	Enhancers	Brain Hippocampus Middle	brain
25	chr2:210287800-210288000	Enhancers	Stomach Smooth Muscle	stomach
26	chr2:210287800-210289000	Active TSS	Fetal Brain Female	brain
27	chr2:210288000-210288200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr2:210288000-210288200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
29	chr2:210288000-210288200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
30	chr2:210288000-210288200	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr2:210288000-210288200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
32	chr2:210288000-210288200	Bivalent/Poised TSS	Primary B cells from cord blood	blood
33	chr2:210288000-210288200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
34	chr2:210288000-210288200	Bivalent Enhancer	Primary T cells from cord blood	blood
35	chr2:210288000-210288200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr2:210288000-210288200	Enhancers	Adipose Nuclei	Adipose
37	chr2:210288000-210288200	Enhancers	Liver	Liver
38	chr2:210288000-210288200	Enhancers	Esophagus	oesophagus
39	chr2:210288000-210288200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
40	chr2:210288000-210288200	Active TSS	Fetal Brain Male	brain
41	chr2:210288000-210288200	Enhancers	Fetal Lung	lung
42	chr2:210288000-210288200	Enhancers	Lung	lung
43	chr2:210288000-210288200	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr2:210288000-210288200	Enhancers	Thymus	Thymus
45	chr2:210288000-210288200	Bivalent/Poised TSS	Monocytes-CD14+_RO01746	blood
46	chr2:210288000-210288200	Enhancers	NHLF	lung
47	chr2:210288000-210288400	Flanking Active TSS	Primary hematopoietic stem cells	blood
48	chr2:210288000-210288400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr2:210288000-210288400	Flanking Active TSS	Brain Anterior Caudate	brain
50	chr2:210288000-210288400	Flanking Active TSS	Brain Hippocampus Middle	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links