Variant report

Variant	nsv1011990
Chromosome Location	chr2:101039956-101105648
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:623)
CpG islands
(count:427)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:623 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:101044286-101044384	K562	blood:	n/a	n/a
2	ATF2	chr2:101070229-101070599	GM12878	blood:	n/a	n/a
3	ATF2	chr2:101070177-101070721	GM12878	blood:	n/a	n/a
4	BACH1	chr2:101044163-101044461	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr2:101070232-101070637	GM12878	blood:	n/a	n/a
6	BATF	chr2:101051625-101051877	GM12878	blood:	n/a	chr2:101051752-101051763
7	BATF	chr2:101070247-101070581	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:101070309-101070593	GM12878	blood:	n/a	n/a
9	BHLHE40	chr2:101099308-101099490	K562	blood:	n/a	n/a
10	BHLHE40	chr2:101044143-101044365	GM12878	blood:	n/a	n/a
11	CEBPB	chr2:101068063-101068620	HCT-116	colon:	n/a	n/a
12	CEBPB	chr2:101042373-101042679	K562	blood:	n/a	chr2:101042524-101042535
13	CEBPB	chr2:101097505-101097647	HepG2	liver:	n/a	chr2:101097552-101097563
14	CEBPB	chr2:101057596-101057794	MCF-7	breast:	n/a	n/a
15	CEBPB	chr2:101042372-101042659	IMR90	lung:	n/a	chr2:101042524-101042535
16	CEBPB	chr2:101042430-101042664	A549	lung:	n/a	chr2:101042524-101042535
17	CEBPB	chr2:101042385-101042695	HepG2	liver:	n/a	chr2:101042524-101042535
18	CEBPB	chr2:101049196-101049526	HepG2	liver:	n/a	chr2:101049354-101049365
19	CEBPB	chr2:101049200-101049510	IMR90	lung:	n/a	chr2:101049354-101049365
20	CEBPB	chr2:101072477-101072545	HepG2	liver:	n/a	chr2:101072521-101072532
21	CEBPB	chr2:101049254-101049448	K562	blood:	n/a	chr2:101049354-101049365
22	CEBPB	chr2:101093481-101093639	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:101049233-101049500	A549	lung:	n/a	chr2:101049354-101049365
24	CEBPB	chr2:101072376-101072652	Hela-S3	cervix:	n/a	chr2:101072521-101072532
25	CEBPZ	chr2:101072953-101073050	HepG2	liver:	n/a	n/a
26	CHD2	chr2:101087537-101087617	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr2:101044148-101044331	GM12878	blood:	n/a	n/a
28	CTCF	chr2:101099299-101099492	MCF-7	breast:	n/a	chr2:101099387-101099405 chr2:101099390-101099399 chr2:101099389-101099410
29	CTCF	chr2:101044180-101044330	GM12874	blood:	n/a	n/a
30	CTCF	chr2:101100941-101101117	HepG2	liver:	n/a	n/a
31	CTCF	chr2:101044185-101044418	MCF-7	breast:	n/a	n/a
32	CTCF	chr2:101099282-101099502	GM19238	blood:	n/a	chr2:101099387-101099405 chr2:101099390-101099399 chr2:101099389-101099410
33	CTCF	chr2:101057620-101057770	GM12878	blood:	n/a	n/a
34	CTCF	chr2:101099340-101099490	GM12868	blood:	n/a	chr2:101099387-101099405 chr2:101099390-101099399 chr2:101099389-101099410
35	CTCF	chr2:101101031-101101090	HepG2	liver:	n/a	n/a
36	CTCF	chr2:101099267-101099510	K562	blood:	n/a	chr2:101099387-101099405 chr2:101099390-101099399 chr2:101099389-101099410
37	CTCF	chr2:101099320-101099470	MCF-7	breast:	n/a	chr2:101099387-101099405 chr2:101099390-101099399 chr2:101099389-101099410
38	CTCF	chr2:101090640-101090790	WI-38	lung:	n/a	n/a
39	CTCF	chr2:101044180-101044330	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr2:101057549-101057790	K562	blood:	n/a	n/a
41	CTCF	chr2:101099300-101099450	GM12865	blood:	n/a	chr2:101099387-101099405 chr2:101099390-101099399 chr2:101099389-101099410
42	CTCF	chr2:101044200-101044350	GM12875	blood:	n/a	n/a
43	CTCF	chr2:101099196-101099550	K562	blood:	n/a	chr2:101099387-101099405 chr2:101099390-101099399 chr2:101099389-101099410
44	CTCF	chr2:101044209-101044420	GM12878	blood:	n/a	n/a
45	CTCF	chr2:101044155-101044364	T-47D	breast:	n/a	n/a
46	CTCF	chr2:101057498-101057853	GM12878	blood:	n/a	n/a
47	CTCF	chr2:101044131-101044422	K562	blood:	n/a	n/a
48	CTCF	chr2:101099283-101099502	GM12892	blood:	n/a	chr2:101099387-101099405 chr2:101099390-101099399 chr2:101099389-101099410
49	CTCF	chr2:101099260-101099410	GM12871	blood:	n/a	chr2:101099387-101099405 chr2:101099390-101099399 chr2:101099389-101099410
50	CTCF	chr2:101044400-101044550	NB4	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:101086963-101087013	AG09309	skin:	n/a
2	chr2:101087575-101087625	HPAEpiC	pulmonary alveolar:	n/a
3	chr2:101086756-101086806	Hepatocyte	liver:	n/a
4	chr2:101087575-101087625	SAEC	small airway:	n/a
5	chr2:101043210-101043260	Caco-2	colon:	n/a
6	chr2:101043080-101043130	HEEpiC	esophagus:	n/a
7	chr2:101086756-101086806	SAEC	small airway:	n/a
8	chr2:101086963-101087013	U87	brain:	n/a
9	chr2:101087575-101087625	HNPCEpiC	eye:	n/a
10	chr2:101086963-101087013	AG10803	skin:	n/a
11	chr2:101043210-101043260	RPTEC	kidney:	n/a
12	chr2:101086963-101087013	AG04449	skin:	fetal
13	chr2:101043210-101043260	Hela-S3	cervix:	n/a
14	chr2:101086893-101086943	NB4	blood:	n/a
15	chr2:101043080-101043130	PrEC	prostate:	n/a
16	chr2:101043080-101043130	AG09309	skin:	n/a
17	chr2:101086963-101087013	HCF	heart:	n/a
18	chr2:101086963-101087013	K562	blood:	n/a
19	chr2:101043210-101043260	GM19239	blood:	n/a
20	chr2:101043210-101043260	NB4	blood:	n/a
21	chr2:101087575-101087625	MCF-7	breast:	n/a
22	chr2:101043210-101043260	HL-60	blood:	n/a
23	chr2:101043210-101043260	SAEC	small airway:	n/a
24	chr2:101086963-101087013	AoSMC	blood vessel:	n/a
25	chr2:101043080-101043130	Hela-S3	cervix:	n/a
26	chr2:101043080-101043130	MCF-7	breast:	n/a
27	chr2:101086756-101086806	GM06990	blood:	n/a
28	chr2:101086756-101086806	NH-A	brain:	n/a
29	chr2:101086963-101087013	Caco-2	colon:	n/a
30	chr2:101087575-101087625	HUVEC	blood vessel:	n/a
31	chr2:101086756-101086806	HRPEpiC	eye:	n/a
32	chr2:101086756-101086806	NB4	blood:	n/a
33	chr2:101043080-101043130	SK-N-SH_RA	brain:	n/a
34	chr2:101086756-101086806	HCF	heart:	n/a
35	chr2:101087575-101087625	MCF10A-Er-Src	breast:	n/a
36	chr2:101086963-101087013	SKMC	muscle:	n/a
37	chr2:101043080-101043130	BE2_C	brain:	n/a
38	chr2:101086756-101086806	Caco-2	colon:	n/a
39	chr2:101043080-101043130	AG10803	skin:	n/a
40	chr2:101042998-101043048	HMEC	breast:	n/a
41	chr2:101087575-101087625	ProgFib	skin:	n/a
42	chr2:101043210-101043260	BE2_C	brain:	n/a
43	chr2:101086963-101087013	AG09319	gingival:	n/a
44	chr2:101042998-101043048	HIPEpiC	eye:	n/a
45	chr2:101042998-101043048	NH-A	brain:	n/a
46	chr2:101043210-101043260	AG09309	skin:	n/a
47	chr2:101087575-101087625	RPTEC	kidney:	n/a
48	chr2:101086963-101087013	HL-60	blood:	n/a
49	chr2:101086893-101086943	NH-A	brain:	n/a
50	chr2:101043210-101043260	HCPEpiC	choroid plexus:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:101055263..101057422-chr2:101627626..101629711,2	MCF-7	breast:
2	chr2:101058028..101060047-chr2:101063483..101065501,2	MCF-7	breast:
3	chr2:101081235..101083922-chr2:101085954..101088786,3	K562	blood:
4	chr2:101023081..101025478-chr2:101042210..101044979,2	MCF-7	breast:
5	chr2:101100078..101102240-chr2:101176769..101179380,2	K562	blood:
6	chr2:101041152..101044058-chr2:101179314..101180934,2	K562	blood:
7	chr2:101065530..101068470-chr2:101179201..101180858,2	MCF-7	breast:
8	chr2:101058472..101060178-chr2:101158909..101160957,2	MCF-7	breast:
9	chr2:101087589..101089414-chr2:101093302..101095563,2	K562	blood:
10	chr11:62607633..62609138-chr2:101067062..101068582,2	K562	blood:
11	chr2:101043749..101044275-chr2:101055367..101055975,2	K562	blood:
12	chr2:101059954..101062390-chr2:101062791..101065672,2	MCF-7	breast:
13	chr2:101040106..101042486-chr2:101042782..101044958,2	MCF-7	breast:
14	chr2:100939645..100941794-chr2:101040138..101041675,2	MCF-7	breast:
15	chr2:100878634..100879528-chr2:101043813..101044750,3	K562	blood:
16	chr2:101101769..101103821-chr2:101257032..101259375,2	K562	blood:
17	chr11:62608619..62609223-chr2:101067060..101067582,2	Hela-S3	cervix:
18	chr2:100878753..100879520-chr2:101043832..101044773,2	MCF-7	breast:
19	chr2:101029935..101035569-chr2:101035669..101041059,9	MCF-7	breast:
20	chr2:100882939..100884943-chr2:101037829..101040208,2	MCF-7	breast:
21	chr2:101059954..101062390-chr2:101062791..101065672,2	MCF-7	breast:
22	chr2:101040091..101042710-chr2:101047786..101050567,2	K562	blood:
23	chr2:100907128..100908845-chr2:101037649..101040314,2	MCF-7	breast:
24	chr2:101087589..101089414-chr2:101093302..101095563,2	K562	blood:
25	chr2:101065517..101069142-chr2:101179392..101181432,3	MCF-7	breast:
26	chr2:101043749..101044275-chr2:101055367..101055975,2	K562	blood:
27	chr2:101033457..101036653-chr2:101042804..101046394,3	MCF-7	breast:
28	chr2:101058028..101060047-chr2:101063483..101065501,2	MCF-7	breast:
29	chr2:101032643..101036022-chr2:101036491..101040981,5	K562	blood:

No data

Variant related genes	Relation type
NMS	TF binding region
ENSG00000238029	TF binding region
NMS	CpG island
ENSG00000238029	CpG island
ENSG00000238029	chromatin interactions
ENSG00000204640	chromatin interactions
ENSG00000115539	chromatin interactions
ENSG00000115526	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 1532 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1532 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2309801	chr2:101039956-101039957	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs765088	chr2:101040011-101040012	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs139823497	chr2:101040039-101040040	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs537958061	chr2:101040040-101040041	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs188799088	chr2:101040045-101040046	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs560635045	chr2:101040107-101040108	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs370829624	chr2:101040208-101040209	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs192862265	chr2:101040250-101040251	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs79083202	chr2:101040297-101040298	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs562871172	chr2:101040301-101040302	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs531858344	chr2:101040331-101040332	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs371931723	chr2:101040344-101040345	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs375075380	chr2:101040359-101040360	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs374978968	chr2:101040360-101040361	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs369278328	chr2:101040363-101040364	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs540406261	chr2:101040448-101040449	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs568513924	chr2:101040545-101040546	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs534400069	chr2:101040554-101040555	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs557237270	chr2:101040659-101040660	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs185077648	chr2:101040755-101040756	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs547215773	chr2:101040756-101040757	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs187950050	chr2:101040797-101040798	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs564300312	chr2:101040809-101040810	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs143124749	chr2:101040817-101040818	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs545555861	chr2:101040866-101040867	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs556165476	chr2:101040868-101040869	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs576417871	chr2:101040890-101040891	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs191524360	chr2:101040920-101040921	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs116012314	chr2:101040953-101040954	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs116969782	chr2:101041026-101041027	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs572195361	chr2:101041086-101041087	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs146180745	chr2:101041087-101041088	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs560417992	chr2:101041089-101041090	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs183638682	chr2:101041092-101041093	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs545815312	chr2:101041116-101041117	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs562509949	chr2:101041160-101041161	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs2118466	chr2:101041163-101041164	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs116492454	chr2:101041206-101041207	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs562395315	chr2:101041210-101041211	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs527913643	chr2:101041214-101041215	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs56211325	chr2:101041230-101041231	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs570581428	chr2:101041238-101041239	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs539502618	chr2:101041247-101041248	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs549810361	chr2:101041259-101041260	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs188053403	chr2:101041276-101041277	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs535430064	chr2:101041351-101041352	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs371115290	chr2:101041362-101041363	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs7596073	chr2:101041367-101041368	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs572291869	chr2:101041395-101041396	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs111912091	chr2:101041405-101041406	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

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	17483303	CNVD
Medulloblastoma	20607354	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
Ovarian cancer	21781307	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
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:101034600-101043000	Weak transcription	Placenta	Placenta
2	chr2:101034800-101043800	Weak transcription	Brain Cingulate Gyrus	brain
3	chr2:101035000-101040000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr2:101035200-101040400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr2:101038800-101040000	Enhancers	Colon Smooth Muscle	Colon
6	chr2:101039400-101040000	Weak transcription	Fetal Lung	lung
7	chr2:101039600-101041000	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr2:101039600-101041000	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr2:101039800-101041200	Enhancers	NHDF-Ad	bronchial
10	chr2:101040000-101040200	Enhancers	Fetal Lung	lung
11	chr2:101040000-101040400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr2:101040000-101040800	Weak transcription	Colon Smooth Muscle	Colon
13	chr2:101040800-101041200	Enhancers	H1 Cell Line	embryonic stem cell
14	chr2:101040800-101041200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr2:101040800-101041200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr2:101040800-101041400	Enhancers	Stomach Smooth Muscle	stomach
17	chr2:101040800-101042200	Enhancers	Colon Smooth Muscle	Colon
18	chr2:101041000-101041200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr2:101041000-101041400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr2:101041000-101041400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr2:101041000-101041400	Enhancers	Rectal Smooth Muscle	rectum
22	chr2:101041000-101042000	Enhancers	Fetal Stomach	stomach
23	chr2:101041000-101042000	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr2:101041000-101044400	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr2:101041600-101043200	Enhancers	Primary hematopoietic stem cells	blood
26	chr2:101042000-101042800	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr2:101042000-101043000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
28	chr2:101042800-101043200	Enhancers	Fetal Brain Male	brain
29	chr2:101043000-101043400	Enhancers	Placenta	Placenta
30	chr2:101043000-101044400	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr2:101043800-101044000	Enhancers	Colon Smooth Muscle	Colon
32	chr2:101043800-101044200	Enhancers	Brain Cingulate Gyrus	brain
33	chr2:101044000-101044400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr2:101044000-101044400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr2:101044400-101045600	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr2:101045800-101046000	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr2:101046000-101046600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr2:101051200-101052800	Enhancers	Fetal Heart	heart
39	chr2:101057200-101057600	Enhancers	Fetal Brain Male	brain
40	chr2:101062600-101063200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr2:101064200-101064600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr2:101064200-101064600	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr2:101064200-101064800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:101065800-101066400	Active TSS	Pancreas	Pancrea
45	chr2:101069600-101071200	Enhancers	GM12878-XiMat	blood
46	chr2:101070400-101071000	Enhancers	Colon Smooth Muscle	Colon
47	chr2:101073400-101074600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr2:101076800-101078200	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr2:101079400-101080000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr2:101085000-101085200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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