Variant report

Variant	nsv1007821
Chromosome Location	chr2:206333129-206465451
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:794)
CpG islands
(count:610)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:206375215-206375434	HepG2	liver:	n/a	n/a
2	ATF1	chr2:206458821-206458937	K562	blood:	n/a	n/a
3	ATF2	chr2:206346954-206347775	H1-hESC	embryonic stem cell:	n/a	chr2:206347531-206347545 chr2:206347533-206347544
4	ATF2	chr2:206347117-206347865	H1-hESC	embryonic stem cell:	n/a	chr2:206347531-206347545 chr2:206347533-206347544
5	BATF	chr2:206338534-206338770	GM12878	blood:	n/a	n/a
6	BCL11A	chr2:206347165-206347444	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr2:206458763-206458813	K562	blood:	n/a	n/a
8	BRCA1	chr2:206395249-206395257	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:206425028-206425228	HepG2	liver:	n/a	chr2:206425163-206425176 chr2:206425164-206425175
10	CEBPB	chr2:206421348-206421388	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr2:206361295-206361315	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr2:206438872-206439210	IMR90	lung:	n/a	n/a
13	CEBPB	chr2:206445116-206445628	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:206431402-206431609	Hela-S3	cervix:	n/a	chr2:206431474-206431485
15	CEBPB	chr2:206397179-206397398	HepG2	liver:	n/a	chr2:206397309-206397320
16	CEBPB	chr2:206431385-206431627	HepG2	liver:	n/a	chr2:206431474-206431485
17	CEBPB	chr2:206455328-206455816	IMR90	lung:	n/a	n/a
18	CEBPB	chr2:206395343-206395511	A549	lung:	n/a	n/a
19	CEBPB	chr2:206451416-206451677	A549	lung:	n/a	chr2:206451545-206451558 chr2:206451545-206451558 chr2:206451547-206451558 chr2:206451542-206451559 chr2:206451547-206451558
20	CEBPB	chr2:206439056-206439104	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr2:206361484-206361926	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:206431272-206431624	MCF-7	breast:	n/a	chr2:206431474-206431485
23	CEBPB	chr2:206431328-206431652	IMR90	lung:	n/a	chr2:206431474-206431485
24	CHD2	chr2:206428486-206428708	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr2:206346991-206347849	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr2:206347041-206347841	H1-hESC	embryonic stem cell:	n/a	chr2:206347532-206347545
27	CREB1	chr2:206347169-206347777	H1-hESC	embryonic stem cell:	n/a	chr2:206347532-206347545
28	CTBP2	chr2:206346991-206347614	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr2:206428460-206428610	NHDF-neo	bronchial:	n/a	n/a
30	CTCF	chr2:206429580-206429730	GM12872	blood:	n/a	n/a
31	CTCF	chr2:206404460-206404610	HUVEC	blood vessel:	n/a	chr2:206404535-206404542
32	CTCF	chr2:206361200-206361350	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr2:206428480-206428630	A549	lung:	n/a	n/a
34	CTCF	chr2:206429220-206429370	HMEC	breast:	n/a	n/a
35	CTCF	chr2:206361320-206361470	BJ	skin:	n/a	n/a
36	CTCF	chr2:206412120-206412270	NHEK	skin:	n/a	n/a
37	CTCF	chr2:206428472-206428622	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr2:206429260-206429410	BE2_C	brain:	n/a	n/a
39	CTCF	chr2:206428420-206428570	AG09309	skin:	n/a	n/a
40	CTCF	chr2:206404419-206404643	MCF-7	breast:	n/a	chr2:206404535-206404542
41	CTCF	chr2:206392480-206392630	HAc	cerebellar:	n/a	n/a
42	CTCF	chr2:206429560-206429710	MCF-7	breast:	n/a	n/a
43	CTCF	chr2:206428480-206428630	NHEK	skin:	n/a	n/a
44	CTCF	chr2:206428560-206428710	HFF	foreskin:	n/a	n/a
45	CTCF	chr2:206404440-206404590	HEK293	kidney:	n/a	chr2:206404535-206404542
46	CTCF	chr2:206428490-206428653	GM20000	blood:	n/a	n/a
47	CTCF	chr2:206429580-206429730	AG04449	skin:	n/a	n/a
48	CTCF	chr2:206428470-206428692	GM12892	blood:	n/a	n/a
49	CTCF	chr2:206428480-206428630	HVMF	connective:	n/a	n/a
50	CTCF	chr2:206361240-206361390	HMF	breast:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:206349064-206349114	ovcar-3	ovarian:	n/a
2	chr2:206349064-206349114	Hela-S3	cervix:	n/a
3	chr2:206455430-206455480	AG09309	skin:	n/a
4	chr2:206336536-206336586	PANC-1	pancreas:	n/a
5	chr2:206336536-206336586	AG09319	gingival:	n/a
6	chr2:206360335-206360385	SK-N-MC	brain:	n/a
7	chr2:206375718-206375768	MCF10A-Er-Src	breast:	n/a
8	chr2:206360335-206360385	SKMC	muscle:	n/a
9	chr2:206336536-206336586	HRPEpiC	eye:	n/a
10	chr2:206336536-206336586	HL-60	blood:	n/a
11	chr2:206349064-206349114	SK-N-MC	brain:	n/a
12	chr2:206336536-206336586	HCPEpiC	choroid plexus:	n/a
13	chr2:206455430-206455480	H1-hESC	embryonic stem cell:	embryo
14	chr2:206455430-206455480	HRPEpiC	eye:	n/a
15	chr2:206411031-206411081	AoSMC	blood vessel:	n/a
16	chr2:206336536-206336586	SK-N-MC	brain:	n/a
17	chr2:206347777-206347827	HEK293	kidney:	embryo
18	chr2:206411031-206411081	NH-A	brain:	n/a
19	chr2:206421582-206421632	GM06990	blood:	n/a
20	chr2:206360335-206360385	AG09319	gingival:	n/a
21	chr2:206411031-206411081	SK-N-SH_RA	brain:	n/a
22	chr2:206349708-206349758	Hela-S3	cervix:	n/a
23	chr2:206347777-206347827	HCT-116	colon:	n/a
24	chr2:206349708-206349758	SKMC	muscle:	n/a
25	chr2:206349708-206349758	HCPEpiC	choroid plexus:	n/a
26	chr2:206349708-206349758	AG04450	lung:	fetal
27	chr2:206347777-206347827	HRPEpiC	eye:	n/a
28	chr2:206349064-206349114	HCF	heart:	n/a
29	chr2:206375718-206375768	AG09319	gingival:	n/a
30	chr2:206360335-206360385	GM12878	blood:	n/a
31	chr2:206349708-206349758	NHDF-neo	bronchial:	n/a
32	chr2:206347777-206347827	HUVEC	blood vessel:	n/a
33	chr2:206336536-206336586	SK-N-SH	brain:	n/a
34	chr2:206360335-206360385	NB4	blood:	n/a
35	chr2:206455430-206455480	CMK	blood:	n/a
36	chr2:206360335-206360385	HMEC	breast:	n/a
37	chr2:206342226-206342276	BJ	skin:	n/a
38	chr2:206336536-206336586	H1-hESC	embryonic stem cell:	embryo
39	chr2:206349064-206349114	MCF-7	breast:	n/a
40	chr2:206375718-206375768	GM12891	blood:	n/a
41	chr2:206342226-206342276	GM06990	blood:	n/a
42	chr2:206360335-206360385	GM12891	blood:	n/a
43	chr2:206349064-206349114	A549	lung:	n/a
44	chr2:206411031-206411081	SK-N-SH	brain:	n/a
45	chr2:206375718-206375768	AG09309	skin:	n/a
46	chr2:206342226-206342276	LNCaP	prostate:	n/a
47	chr2:206411031-206411081	HNPCEpiC	eye:	n/a
48	chr2:206349064-206349114	HRPEpiC	eye:	n/a
49	chr2:206455430-206455480	GM12878	blood:	n/a
50	chr2:206336536-206336586	SKMC	muscle:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:206426191..206428311-chr2:206429496..206431133,2	MCF-7	breast:
2	chr2:206390074..206392954-chr20:38552054..38553554,2	MCF-7	breast:
3	chr2:206426191..206428311-chr2:206429496..206431133,2	MCF-7	breast:
4	chr2:206387607..206389852-chr2:206392892..206394684,2	MCF-7	breast:
5	chr2:206461465..206461972-chr2:206750084..206750604,2	MCF-7	breast:
6	chr2:206395199..206396728-chr2:206401067..206403595,2	MCF-7	breast:
7	chr2:206341022..206343808-chr2:206347982..206349930,2	K562	blood:
8	chr2:206404142..206404986-chr2:206540332..206541161,2	MCF-7	breast:
9	chr2:206400876..206403265-chr2:206407681..206410010,2	MCF-7	breast:
10	chr2:206359433..206361731-chr2:206363684..206366442,2	MCF-7	breast:
11	chr2:206341022..206343808-chr2:206347982..206349930,2	K562	blood:
12	chr2:206433786..206435982-chr2:206449745..206451830,2	MCF-7	breast:
13	chr2:206382732..206385527-chr2:206385963..206387907,2	K562	blood:
14	chr2:206336911..206339253-chr3:64082840..64085737,2	MCF-7	breast:
15	chr2:206400876..206403265-chr2:206407681..206410010,2	MCF-7	breast:
16	chr2:206359433..206361731-chr2:206363684..206366442,2	MCF-7	breast:
17	chr2:206456715..206459134-chr2:206471272..206472956,2	MCF-7	breast:
18	chr2:206433786..206435982-chr2:206449745..206451830,2	MCF-7	breast:
19	chr2:206382732..206385527-chr2:206385963..206387907,2	K562	blood:
20	chr2:206358113..206360299-chr6:27112418..27114699,2	MCF-7	breast:
21	chr2:206395199..206396728-chr2:206401067..206403595,2	MCF-7	breast:
22	chr2:206437172..206439610-chr2:206443059..206445348,2	K562	blood:
23	chr2:206387607..206389852-chr2:206392892..206394684,2	MCF-7	breast:
24	chr2:206437172..206439610-chr2:206443059..206445348,2	K562	blood:

No data

Variant related genes	Relation type
PARD3B	TF binding region
PARD3B	CpG island
ENSG00000197903	chromatin interactions
ENSG00000241572	chromatin interactions

Extended variants
information (count: 4698 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:4698 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375274778	chr2:206333130-206333131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551276697	chr2:206333133-206333134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368954694	chr2:206333144-206333145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372674144	chr2:206333213-206333214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530404592	chr2:206333271-206333272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189065769	chr2:206333283-206333284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181938039	chr2:206333300-206333301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186312566	chr2:206333303-206333304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368116367	chr2:206333304-206333305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559724636	chr2:206333313-206333314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372364392	chr2:206333366-206333367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538498963	chr2:206333388-206333389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375950520	chr2:206333394-206333395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370881134	chr2:206333408-206333409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs78538940	chr2:206333416-206333417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374370924	chr2:206333466-206333467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116131482	chr2:206333467-206333468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535354971	chr2:206333475-206333476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368809788	chr2:206333478-206333479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191103202	chr2:206333488-206333489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs372965411	chr2:206333528-206333529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs377377305	chr2:206333603-206333604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561649430	chr2:206333618-206333619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144851143	chr2:206333638-206333639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs75789418	chr2:206333691-206333692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76646191	chr2:206333703-206333704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372823302	chr2:206333704-206333705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368901840	chr2:206333705-206333706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528946705	chr2:206333764-206333765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528459311	chr2:206333787-206333788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138765705	chr2:206333809-206333810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561714221	chr2:206333820-206333821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377239024	chr2:206333847-206333848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542495304	chr2:206333869-206333870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142758652	chr2:206333883-206333884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527854598	chr2:206333912-206333913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs180751591	chr2:206333940-206333941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115060748	chr2:206334070-206334071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185986567	chr2:206334071-206334072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7340265	chr2:206334094-206334095	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs568393745	chr2:206334180-206334181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191313223	chr2:206334228-206334229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553613843	chr2:206334242-206334243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565559710	chr2:206334253-206334254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183230135	chr2:206334287-206334288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs557917926	chr2:206334295-206334296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146073226	chr2:206334302-206334303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543501870	chr2:206334324-206334325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200096797	chr2:206334369-206334370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12619568	chr2:206334424-206334425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	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
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	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
Papillary thyroid carcinoma	22161024	CNVD
Cervical cancer	21062161	CNVD
Intracranial aneurysm	16715129	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	16573809	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Non-small cell lung cancer	21829676	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:819 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:206328600-206339000	Weak transcription	HSMM	muscle
2	chr2:206328800-206336600	Weak transcription	Fetal Muscle Leg	muscle
3	chr2:206330600-206336400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr2:206331000-206334600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr2:206331400-206336400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr2:206331400-206336400	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr2:206331600-206334800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr2:206331800-206335400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr2:206332000-206335400	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr2:206334600-206335600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr2:206334800-206335400	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr2:206334800-206337000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr2:206335000-206337200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr2:206335000-206337400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr2:206335200-206335400	Enhancers	H9 Cell Line	embryonic stem cell
16	chr2:206335400-206335600	Enhancers	H1 Cell Line	embryonic stem cell
17	chr2:206335400-206335600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr2:206335400-206336400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr2:206335400-206336600	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr2:206335600-206335800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr2:206335600-206336000	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr2:206335600-206336400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr2:206335600-206336600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr2:206336000-206337000	Enhancers	H1 Cell Line	embryonic stem cell
25	chr2:206336400-206336800	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr2:206336400-206336800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr2:206336400-206337000	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr2:206336400-206337000	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr2:206336400-206337200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr2:206336600-206337000	Enhancers	H9 Cell Line	embryonic stem cell
31	chr2:206336600-206337400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr2:206336800-206337000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr2:206336800-206346000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr2:206337000-206338600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:206337000-206341200	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr2:206337000-206346000	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr2:206337400-206345600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr2:206338600-206341000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr2:206338600-206341400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr2:206338800-206341000	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr2:206339000-206340400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr2:206339000-206340800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr2:206339000-206340800	Enhancers	HSMM	muscle
44	chr2:206339000-206340800	Enhancers	NHDF-Ad	bronchial
45	chr2:206339200-206340000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr2:206339200-206340000	Enhancers	Muscle Satellite Cultured Cells	--
47	chr2:206339200-206340200	Enhancers	Osteobl	bone
48	chr2:206339200-206340400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr2:206339400-206340000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr2:206339400-206340000	Enhancers	NH-A	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links