Variant report

Variant	nsv468579
Chromosome Location	chr11:59814287-59975400
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1624)
CpG islands
(count:1894)
Chromatin interactive
region (count:43)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1624 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:59884218-59884222	K562	blood:	n/a	n/a
2	ARID3A	chr11:59893449-59893832	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:59961305-59961874	K562	blood:	n/a	n/a
4	ARID3A	chr11:59865771-59866375	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:59888692-59888945	K562	blood:	n/a	n/a
6	ARID3A	chr11:59892317-59892493	K562	blood:	n/a	n/a
7	ARID3A	chr11:59879254-59879456	K562	blood:	n/a	n/a
8	ARID3A	chr11:59824079-59824209	K562	blood:	n/a	n/a
9	ARID3A	chr11:59963500-59963933	K562	blood:	n/a	n/a
10	ATF1	chr11:59961182-59961881	K562	blood:	n/a	n/a
11	ATF1	chr11:59826690-59826742	K562	blood:	n/a	n/a
12	ATF1	chr11:59888743-59889069	K562	blood:	n/a	n/a
13	ATF1	chr11:59846322-59846529	K562	blood:	n/a	n/a
14	ATF1	chr11:59823710-59824276	K562	blood:	n/a	n/a
15	ATF1	chr11:59894706-59895192	K562	blood:	n/a	n/a
16	ATF1	chr11:59853455-59853752	K562	blood:	n/a	n/a
17	ATF1	chr11:59966260-59966374	K562	blood:	n/a	n/a
18	ATF1	chr11:59898038-59898339	K562	blood:	n/a	n/a
19	ATF2	chr11:59961061-59962002	GM12878	blood:	n/a	n/a
20	ATF2	chr11:59961033-59961926	GM12878	blood:	n/a	n/a
21	ATF2	chr11:59974037-59974498	GM12878	blood:	n/a	n/a
22	ATF2	chr11:59973936-59974476	GM12878	blood:	n/a	n/a
23	ATF2	chr11:59963398-59963814	GM12878	blood:	n/a	n/a
24	ATF2	chr11:59972347-59972853	GM12878	blood:	n/a	n/a
25	ATF2	chr11:59943277-59943643	GM12878	blood:	n/a	n/a
26	ATF2	chr11:59972308-59972822	GM12878	blood:	n/a	n/a
27	ATF2	chr11:59963265-59963798	GM12878	blood:	n/a	n/a
28	ATF2	chr11:59952572-59953034	GM12878	blood:	n/a	n/a
29	ATF3	chr11:59826579-59826826	K562	blood:	n/a	n/a
30	ATF3	chr11:59961582-59961838	K562	blood:	n/a	n/a
31	ATF3	chr11:59894590-59895127	K562	blood:	n/a	n/a
32	BACH1	chr11:59894643-59895021	K562	blood:	n/a	n/a
33	BATF	chr11:59935878-59936155	GM12878	blood:	n/a	chr11:59936013-59936024
34	BATF	chr11:59933083-59933319	GM12878	blood:	n/a	chr11:59933195-59933206 chr11:59933200-59933210 chr11:59933196-59933206
35	BATF	chr11:59826577-59826779	GM12878	blood:	n/a	chr11:59826708-59826719
36	BATF	chr11:59974039-59974489	GM12878	blood:	n/a	chr11:59974317-59974328
37	BATF	chr11:59972298-59972785	GM12878	blood:	n/a	n/a
38	BATF	chr11:59826600-59826779	GM12878	blood:	n/a	chr11:59826708-59826719
39	BATF	chr11:59952718-59952946	GM12878	blood:	n/a	n/a
40	BATF	chr11:59972355-59972759	GM12878	blood:	n/a	n/a
41	BATF	chr11:59943289-59943622	GM12878	blood:	n/a	n/a
42	BATF	chr11:59960008-59960287	GM12878	blood:	n/a	chr11:59960111-59960122
43	BATF	chr11:59974004-59974576	GM12878	blood:	n/a	chr11:59974317-59974328 chr11:59974547-59974560
44	BATF	chr11:59932241-59932528	GM12878	blood:	n/a	n/a
45	BATF	chr11:59963278-59963657	GM12878	blood:	n/a	n/a
46	BATF	chr11:59933032-59933326	GM12878	blood:	n/a	chr11:59933195-59933206 chr11:59933200-59933210 chr11:59933196-59933206
47	BATF	chr11:59961129-59961771	GM12878	blood:	n/a	n/a
48	BATF	chr11:59952711-59952981	GM12878	blood:	n/a	n/a
49	BCL11A	chr11:59943312-59943754	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:59952677-59953041	GM12878	blood:	n/a	n/a

(count:1894 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:59815177-59815227	HNPCEpiC	eye:	n/a
2	chr11:59824089-59824139	NT2-D1	testis:	n/a
3	chr11:59952134-59952184	NB4	blood:	n/a
4	chr11:59815177-59815227	HNPCEpiC	eye:	n/a
5	chr11:59824089-59824139	NT2-D1	testis:	n/a
6	chr11:59952134-59952184	NB4	blood:	n/a
7	chr11:59969032-59969082	PrEC	prostate:	n/a
8	chr11:59836817-59836867	U87	brain:	n/a
9	chr11:59824089-59824139	GM19239	blood:	n/a
10	chr11:59856225-59856275	AG10803	skin:	n/a
11	chr11:59824089-59824139	HUVEC	blood vessel:	n/a
12	chr11:59838540-59838590	IMR90	lung:	fetal
13	chr11:59836817-59836867	GM12892	blood:	n/a
14	chr11:59841011-59841061	HRE	kidney:	n/a
15	chr11:59950068-59950118	NHBE	bronchial:	n/a
16	chr11:59815177-59815227	HRE	kidney:	n/a
17	chr11:59824116-59824166	AG04449	skin:	fetal
18	chr11:59836817-59836867	H1-hESC	embryonic stem cell:	embryo
19	chr11:59824161-59824211	A549	lung:	n/a
20	chr11:59861219-59861269	NHDF-neo	bronchial:	n/a
21	chr11:59953045-59953095	GM12891	blood:	n/a
22	chr11:59951663-59951713	AG09319	gingival:	n/a
23	chr11:59951557-59951607	PFSK-1	brain:	n/a
24	chr11:59824116-59824166	GM12892	blood:	n/a
25	chr11:59951663-59951713	HIPEpiC	eye:	n/a
26	chr11:59942032-59942082	MCF10A-Er-Src	breast:	n/a
27	chr11:59824116-59824166	SAEC	small airway:	n/a
28	chr11:59951557-59951607	PANC-1	pancreas:	n/a
29	chr11:59836817-59836867	HRCEpiC	kidney:	n/a
30	chr11:59856225-59856275	NHDF-neo	bronchial:	n/a
31	chr11:59951663-59951713	HCM	heart:	n/a
32	chr11:59950525-59950575	AG04450	lung:	fetal
33	chr11:59824110-59824160	GM19239	blood:	n/a
34	chr11:59953045-59953095	CMK	blood:	n/a
35	chr11:59824161-59824211	NB4	blood:	n/a
36	chr11:59953045-59953095	NB4	blood:	n/a
37	chr11:59950525-59950575	HMEC	breast:	n/a
38	chr11:59864308-59864358	T-47D	breast:	n/a
39	chr11:59824161-59824211	ECC-1	luminal epithelium:	n/a
40	chr11:59953045-59953095	AG04449	skin:	fetal
41	chr11:59951557-59951607	HCM	heart:	n/a
42	chr11:59841290-59841340	H1-hESC	embryonic stem cell:	embryo
43	chr11:59841290-59841340	HRPEpiC	eye:	n/a
44	chr11:59951663-59951713	AG09309	skin:	n/a
45	chr11:59822765-59822815	HEEpiC	esophagus:	n/a
46	chr11:59815177-59815227	GM19239	blood:	n/a
47	chr11:59951663-59951713	ovcar-3	ovarian:	n/a
48	chr11:59815177-59815227	HEEpiC	esophagus:	n/a
49	chr11:59950068-59950118	HCPEpiC	choroid plexus:	n/a
50	chr11:59950068-59950118	GM06990	blood:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:59857259..59859045-chr11:59866895..59868589,2	K562	blood:
2	chr11:59926779..59928855-chr11:59938111..59940679,2	K562	blood:
3	chr11:59885540..59886539-chr11:59960885..59961593,3	MCF-7	breast:
4	chr11:59905623..59908151-chr11:59911648..59914024,2	K562	blood:
5	chr11:59905623..59908151-chr11:59911648..59914024,2	K562	blood:
6	chr11:59590238..59591135-chr11:59897588..59898633,5	MCF-7	breast:
7	chr11:59835891..59838239-chr11:59840750..59843127,2	K562	blood:
8	chr11:59926973..59929170-chr11:59934444..59937067,2	K562	blood:
9	chr11:59880513..59883091-chr11:59889484..59891627,2	MCF-7	breast:
10	chr11:59521183..59522129-chr11:59897665..59898553,3	K562	blood:
11	chr11:59899268..59901225-chr11:59929250..59931810,2	K562	blood:
12	chr11:59822049..59824288-chr11:59826581..59828945,2	K562	blood:
13	chr11:59899268..59901225-chr11:59929250..59931810,2	K562	blood:
14	chr11:59889345..59891976-chr11:59896394..59897980,2	K562	blood:
15	chr11:59885540..59886539-chr11:59960885..59961593,3	MCF-7	breast:
16	chr11:59915996..59916912-chr11:59960707..59961353,2	K562	blood:
17	chr11:59847145..59850103-chr11:59877853..59879913,2	K562	blood:
18	chr11:59822049..59824288-chr11:59826581..59828945,2	K562	blood:
19	chr11:59590156..59591101-chr11:59960804..59961684,4	MCF-7	breast:
20	chr11:59524342..59526503-chr11:59895914..59898117,2	K562	blood:
21	chr11:59803708..59805688-chr11:59908661..59910786,2	K562	blood:
22	chr11:59909863..59911734-chr11:59915341..59917142,2	K562	blood:
23	chr11:59834202..59837077-chr11:59837940..59839542,2	K562	blood:
24	chr11:59838090..59840392-chr11:59840842..59843824,3	K562	blood:
25	chr11:59886056..59888504-chr11:59892263..59894071,2	K562	blood:
26	chr11:59880513..59883091-chr11:59889484..59891627,2	MCF-7	breast:
27	chr11:59857259..59859045-chr11:59866895..59868589,2	K562	blood:
28	chr11:59877470..59879979-chr11:59886517..59889179,2	K562	blood:
29	chr11:59855869..59858182-chr11:59858719..59861212,2	K562	blood:
30	chr11:59886056..59888504-chr11:59892263..59894071,2	K562	blood:
31	chr11:59929729..59931318-chr11:59936371..59938548,3	K562	blood:
32	chr11:59929729..59931318-chr11:59936371..59938548,3	K562	blood:
33	chr11:59936023..59937006-chr11:59960779..59961684,2	MCF-7	breast:
34	chr11:59915996..59916912-chr11:59960707..59961353,2	K562	blood:
35	chr11:59909863..59911734-chr11:59915341..59917142,2	K562	blood:
36	chr11:59889345..59891976-chr11:59896394..59897980,2	K562	blood:
37	chr11:59589954..59591189-chr11:59897601..59898679,5	K562	blood:
38	chr11:59877470..59879979-chr11:59886517..59889179,2	K562	blood:
39	chr11:59878766..59880591-chr11:59882568..59884421,2	K562	blood:
40	chr11:59936023..59937006-chr11:59960779..59961684,2	MCF-7	breast:
41	chr11:59847145..59850103-chr11:59877853..59879913,2	K562	blood:
42	chr11:59878766..59880591-chr11:59882568..59884421,2	K562	blood:
43	chr11:59838090..59840392-chr11:59840842..59843824,3	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MS4A4E-1	chr11:59946964-59949214	NONHSAT021562
2	lnc-MS4A4E-1	chr11:59947304-59947438	NONHSAT021561
3	lnc-PLAC1L-2	chr11:59828963-59828971	NONHSAT021555
4	lnc-PLAC1L-2	chr11:59828405-59828789	NONHSAT021555
5	lnc-MS4A4E-1	chr11:59950451-59950556	NONHSAT021561
6	lnc-MS4A3-2	chr11:59861438-59861535	NONHSAT021558
7	lnc-MS4A4E-1	chr11:59950278-59950804	NONHSAT021563
8	lnc-MS4A4E-1	chr11:59950643-59950804	NONHSAT021564
9	lnc-MS4A6A-1	chr11:59927752-59927855	ENSG00000254952
10	lnc-MS4A2-1	chr11:59837677-59838454	NONHSAT021556
11	lnc-MS4A6A-1	chr11:59928198-59928295	ENSG00000254952
12	lnc-MS4A3-2	chr11:59857834-59857943	NONHSAT021558
13	lnc-MS4A4E-1	chr11:59951793-59952139	NONHSAT021564
14	lnc-MS4A3-2	chr11:59860266-59860321	NONHSAT021558
15	lnc-MS4A6A-1	chr11:59927160-59927342	ENSG00000254952
16	lnc-MS4A3-2	chr11:59860874-59861031	NONHSAT021558
17	lnc-MS4A4E-1	chr11:59945644-59945789	NONHSAT021561
18	lnc-MS4A4E-1	chr11:59949054-59949214	NONHSAT021561
19	lnc-MS4A3-2	chr11:59863032-59863060	NONHSAT021558
20	lnc-MS4A2-1	chr11:59837004-59837148	NONHSAT021556
21	lnc-MS4A4E-1	chr11:59950451-59950615	NONHSAT021562
22	lnc-MS4A4E-1	chr11:59951195-59951216	NONHSAT021563

No data

Variant related genes	Relation type
MS4A2	TF binding region
MS4A3	TF binding region
ENSG00000254952	TF binding region
ENSG00000255331	TF binding region
MS4A6A	TF binding region
MS4A2	CpG island
MS4A3	CpG island
ENSG00000254952	CpG island
ENSG00000255331	CpG island
MS4A6A	CpG island
ENSG00000149516	chromatin interactions
ENSG00000254952	chromatin interactions
ENSG00000149534	chromatin interactions
SENP1	miRNA target sites
REV3L	miRNA target sites
PDCD4	miRNA target sites
CCNB1	miRNA target sites

Extended variants
information (count: 5985 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5985 , 50 per page) page: 1 2 3 4 5 6 7 ... 120

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2276044	chr11:59814287-59814288	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371443214	chr11:59814301-59814302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs578195962	chr11:59814303-59814304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369422869	chr11:59814325-59814326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369768162	chr11:59814374-59814375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs202100334	chr11:59814393-59814394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182298905	chr11:59814395-59814396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146981402	chr11:59814411-59814412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201529790	chr11:59814439-59814440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs79797080	chr11:59814469-59814470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs373159400	chr11:59814503-59814504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200996938	chr11:59814524-59814525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527766183	chr11:59814562-59814563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147627409	chr11:59814584-59814585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544044188	chr11:59814589-59814590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560941583	chr11:59814606-59814607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs1055506	chr11:59814613-59814614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149153255	chr11:59814793-59814794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112324466	chr11:59814824-59814825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557619931	chr11:59814828-59814829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186737819	chr11:59814851-59814852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546312568	chr11:59814854-59814855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373715286	chr11:59814866-59814867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143295946	chr11:59814878-59814879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146949348	chr11:59814909-59814910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574253529	chr11:59814923-59814924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148290699	chr11:59814963-59814964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565802558	chr11:59814968-59814969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536344036	chr11:59814981-59814982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554653519	chr11:59815005-59815006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377070126	chr11:59815015-59815016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141427511	chr11:59815022-59815023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569107635	chr11:59815054-59815055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371771604	chr11:59815057-59815058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538118445	chr11:59815107-59815108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1144748	chr11:59815117-59815118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12362575	chr11:59815128-59815129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556787103	chr11:59815134-59815135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10501381	chr11:59815139-59815140	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs545617936	chr11:59815155-59815156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554060813	chr11:59815156-59815157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191509253	chr11:59815185-59815186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542663868	chr11:59815188-59815189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560957950	chr11:59815201-59815202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531566219	chr11:59815221-59815222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183989892	chr11:59815275-59815276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188637451	chr11:59815291-59815292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532290667	chr11:59815326-59815327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554194487	chr11:59815357-59815358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373583956	chr11:59815365-59815366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Lung adenocarcinoma	17086460	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Chordoma	18071362	CNVD

Chromatin state (count:694 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59813800-59822400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr11:59816000-59816200	Enhancers	Primary hematopoietic stem cells	blood
3	chr11:59821800-59822400	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr11:59822200-59823600	Enhancers	K562	blood
5	chr11:59822400-59822600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr11:59822400-59822800	Enhancers	Primary hematopoietic stem cells	blood
7	chr11:59822400-59822800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr11:59822400-59823200	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr11:59822400-59823400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
10	chr11:59822400-59826400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr11:59822600-59824200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr11:59822600-59824600	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr11:59822600-59824600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr11:59822800-59823200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr11:59822800-59832000	Weak transcription	Primary hematopoietic stem cells	blood
16	chr11:59823200-59823600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr11:59823200-59824200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr11:59823400-59823800	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr11:59823400-59824200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr11:59823600-59824000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr11:59823600-59824000	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr11:59823600-59824200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr11:59823600-59824800	Flanking Active TSS	K562	blood
24	chr11:59823800-59824200	Enhancers	H1 Cell Line	embryonic stem cell
25	chr11:59823800-59824200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr11:59823800-59824200	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr11:59823800-59824200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr11:59823800-59824200	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr11:59823800-59824600	Enhancers	H9 Cell Line	embryonic stem cell
30	chr11:59823800-59824600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr11:59824000-59824400	Enhancers	Primary B cells from cord blood	blood
32	chr11:59824000-59825000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
33	chr11:59824200-59824600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr11:59824600-59830000	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr11:59824800-59825400	Enhancers	K562	blood
36	chr11:59825000-59827000	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr11:59825400-59825600	Flanking Active TSS	K562	blood
38	chr11:59825600-59826000	Enhancers	K562	blood
39	chr11:59826000-59826400	Flanking Active TSS	K562	blood
40	chr11:59826400-59826600	Enhancers	K562	blood
41	chr11:59826400-59828400	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr11:59826600-59829600	Weak transcription	K562	blood
43	chr11:59827000-59831600	Weak transcription	Monocytes-CD14+_RO01746	blood
44	chr11:59828400-59829800	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr11:59829600-59830600	Enhancers	K562	blood
46	chr11:59829800-59831200	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr11:59830000-59831200	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr11:59830600-59831800	Weak transcription	K562	blood
49	chr11:59830800-59831200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr11:59831200-59831600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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