Variant report

Variant	nsv1007206
Chromosome Location	chr4:10229982-10362490
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:614)
CpG islands
(count:123)
Chromatin interactive
region (count:140)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:614 , 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	chr4:10327415-10328296	K562	blood:	n/a	n/a
2	ARID3A	chr4:10258670-10258802	K562	blood:	n/a	n/a
3	ARID3A	chr4:10242016-10242400	K562	blood:	n/a	n/a
4	ARID3A	chr4:10241023-10241142	K562	blood:	n/a	n/a
5	ARID3A	chr4:10286746-10287065	K562	blood:	n/a	n/a
6	ATF1	chr4:10327430-10328176	K562	blood:	n/a	n/a
7	ATF1	chr4:10241521-10242349	K562	blood:	n/a	n/a
8	ATF3	chr4:10241484-10241931	K562	blood:	n/a	chr4:10241683-10241696
9	ATF3	chr4:10286691-10286995	K562	blood:	n/a	n/a
10	BACH1	chr4:10296613-10296622	K562	blood:	n/a	n/a
11	BACH1	chr4:10306752-10306755	K562	blood:	n/a	n/a
12	BACH1	chr4:10236419-10236458	K562	blood:	n/a	n/a
13	BACH1	chr4:10258150-10258286	K562	blood:	n/a	n/a
14	BACH1	chr4:10291449-10291596	K562	blood:	n/a	n/a
15	BACH1	chr4:10277398-10277423	K562	blood:	n/a	n/a
16	BHLHE40	chr4:10241629-10242291	K562	blood:	n/a	n/a
17	BHLHE40	chr4:10353695-10353726	K562	blood:	n/a	n/a
18	BHLHE40	chr4:10239996-10240058	K562	blood:	n/a	n/a
19	BHLHE40	chr4:10286618-10286919	K562	blood:	n/a	n/a
20	BHLHE40	chr4:10258626-10258818	K562	blood:	n/a	n/a
21	BHLHE40	chr4:10257932-10258036	K562	blood:	n/a	n/a
22	CBX3	chr4:10327059-10328067	K562	blood:	n/a	n/a
23	CBX3	chr4:10327581-10328053	K562	blood:	n/a	n/a
24	CCNT2	chr4:10323672-10323734	K562	blood:	n/a	n/a
25	CCNT2	chr4:10327270-10328296	K562	blood:	n/a	n/a
26	CCNT2	chr4:10346894-10347462	K562	blood:	n/a	n/a
27	CCNT2	chr4:10241954-10242255	K562	blood:	n/a	n/a
28	CCNT2	chr4:10286692-10287087	K562	blood:	n/a	n/a
29	CEBPB	chr4:10255615-10255721	K562	blood:	n/a	n/a
30	CEBPB	chr4:10304348-10304548	K562	blood:	n/a	n/a
31	CEBPB	chr4:10327483-10328195	K562	blood:	n/a	n/a
32	CEBPB	chr4:10326084-10326415	K562	blood:	n/a	chr4:10326229-10326240 chr4:10326226-10326243
33	CEBPB	chr4:10326099-10326299	HepG2	liver:	n/a	chr4:10326229-10326240 chr4:10326226-10326243
34	CEBPB	chr4:10302967-10303233	K562	blood:	n/a	n/a
35	CEBPB	chr4:10311017-10311187	HepG2	liver:	n/a	chr4:10311067-10311078
36	CEBPB	chr4:10267329-10267510	HepG2	liver:	n/a	chr4:10267446-10267457
37	CEBPB	chr4:10327555-10328514	K562	blood:	n/a	n/a
38	CEBPB	chr4:10310964-10311220	K562	blood:	n/a	chr4:10311067-10311078
39	CEBPB	chr4:10267288-10267523	A549	lung:	n/a	chr4:10267446-10267457
40	CEBPD	chr4:10346929-10347528	K562	blood:	n/a	n/a
41	CEBPD	chr4:10241894-10242416	K562	blood:	n/a	n/a
42	CEBPD	chr4:10346907-10347486	K562	blood:	n/a	n/a
43	CEBPD	chr4:10327579-10328268	K562	blood:	n/a	n/a
44	CEBPD	chr4:10327575-10328187	K562	blood:	n/a	n/a
45	CEBPD	chr4:10241866-10242444	K562	blood:	n/a	n/a
46	CHD2	chr4:10335543-10335846	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr4:10330393-10330408	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr4:10256718-10256724	K562	blood:	n/a	n/a
49	CHD2	chr4:10241787-10242039	K562	blood:	n/a	n/a
50	CREB1	chr4:10327464-10328295	K562	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10335492-10335542	GM12878	blood:	n/a
2	chr4:10335492-10335542	GM12878	blood:	n/a
3	chr4:10335492-10335542	SKMC	muscle:	n/a
4	chr4:10299145-10299195	HCM	heart:	n/a
5	chr4:10299145-10299195	HRE	kidney:	n/a
6	chr4:10335492-10335542	K562	blood:	n/a
7	chr4:10335492-10335542	HAEpiC	amniotic membrane:	n/a
8	chr4:10335492-10335542	HL-60	blood:	n/a
9	chr4:10299145-10299195	ProgFib	skin:	n/a
10	chr4:10299145-10299195	HRCEpiC	kidney:	n/a
11	chr4:10335492-10335542	HepG2	liver:	n/a
12	chr4:10299145-10299195	HCF	heart:	n/a
13	chr4:10299145-10299195	Caco-2	colon:	n/a
14	chr4:10299145-10299195	HUVEC	blood vessel:	n/a
15	chr4:10299145-10299195	Hepatocyte	liver:	n/a
16	chr4:10299145-10299195	SK-N-MC	brain:	n/a
17	chr4:10299145-10299195	Jurkat	blood:	n/a
18	chr4:10299145-10299195	BE2_C	brain:	n/a
19	chr4:10299145-10299195	NHDF-neo	bronchial:	n/a
20	chr4:10335492-10335542	NH-A	brain:	n/a
21	chr4:10299145-10299195	IMR90	lung:	fetal
22	chr4:10335492-10335542	H1-hESC	embryonic stem cell:	embryo
23	chr4:10299145-10299195	GM12891	blood:	n/a
24	chr4:10299145-10299195	HNPCEpiC	eye:	n/a
25	chr4:10299145-10299195	PFSK-1	brain:	n/a
26	chr4:10335492-10335542	HRPEpiC	eye:	n/a
27	chr4:10299145-10299195	AoSMC	blood vessel:	n/a
28	chr4:10335492-10335542	HCPEpiC	choroid plexus:	n/a
29	chr4:10335492-10335542	T-47D	breast:	n/a
30	chr4:10335492-10335542	SAEC	small airway:	n/a
31	chr4:10335492-10335542	U87	brain:	n/a
32	chr4:10299145-10299195	AG09319	gingival:	n/a
33	chr4:10299145-10299195	HIPEpiC	eye:	n/a
34	chr4:10335492-10335542	HMEC	breast:	n/a
35	chr4:10335492-10335542	NB4	blood:	n/a
36	chr4:10335492-10335542	GM12892	blood:	n/a
37	chr4:10335492-10335542	HIPEpiC	eye:	n/a
38	chr4:10335492-10335542	HNPCEpiC	eye:	n/a
39	chr4:10299145-10299195	K562	blood:	n/a
40	chr4:10299145-10299195	PANC-1	pancreas:	n/a
41	chr4:10335492-10335542	A549	lung:	n/a
42	chr4:10299145-10299195	NB4	blood:	n/a
43	chr4:10335492-10335542	HRE	kidney:	n/a
44	chr4:10299145-10299195	HCPEpiC	choroid plexus:	n/a
45	chr4:10335492-10335542	SK-N-SH	brain:	n/a
46	chr4:10335492-10335542	SK-N-MC	brain:	n/a
47	chr4:10299145-10299195	A549	lung:	n/a
48	chr4:10335492-10335542	AG04449	skin:	fetal
49	chr4:10335492-10335542	NHDF-neo	bronchial:	n/a
50	chr4:10335492-10335542	PFSK-1	brain:	n/a

(count:140 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:10283364..10286619-chr4:10288507..10291288,3	K562	blood:
2	chr4:10329017..10330933-chr4:10334130..10336518,2	K562	blood:
3	chr4:10181426..10184302-chr4:10237283..10239761,3	K562	blood:
4	chr4:10254361..10256671-chr4:10262474..10264248,2	K562	blood:
5	chr4:10361623..10363629-chr4:10366755..10368380,2	K562	blood:
6	chr4:10271663..10274322-chr4:10278537..10280895,2	K562	blood:
7	chr4:10174527..10176209-chr4:10240126..10241692,2	K562	blood:
8	chr4:10186571..10188279-chr4:10316070..10319056,2	K562	blood:
9	chr4:10332430..10334686-chr4:10341439..10343470,2	K562	blood:
10	chr4:10242448..10244811-chr4:10340269..10342798,2	K562	blood:
11	chr4:10231830..10233378-chr4:10235064..10237402,2	K562	blood:
12	chr4:10357717..10361613-chr4:10362100..10366101,6	K562	blood:
13	chr4:10180991..10182787-chr4:10327240..10329402,2	K562	blood:
14	chr4:10298581..10300458-chr4:10305111..10307586,2	K562	blood:
15	chr4:10175247..10177327-chr4:10228151..10230198,2	K562	blood:
16	chr4:10306958..10308632-chr4:10319609..10321643,2	K562	blood:
17	chr4:10289644..10291282-chr4:10323806..10326517,2	K562	blood:
18	chr4:10165903..10168762-chr4:10325993..10328173,3	K562	blood:
19	chr4:10326481..10328401-chr4:10338341..10340263,2	K562	blood:
20	chr4:10182494..10184107-chr4:10284696..10287149,2	K562	blood:
21	chr4:10329242..10331797-chr4:10359863..10361623,2	K562	blood:
22	chr4:10332430..10334686-chr4:10341439..10343470,2	K562	blood:
23	chr4:10181799..10184639-chr4:10262185..10264664,2	K562	blood:
24	chr4:10293712..10297687-chr4:10307102..10309576,3	K562	blood:
25	chr4:10312898..10315516-chr4:10318323..10320073,4	K562	blood:
26	chr4:10298581..10300458-chr4:10305111..10307586,2	K562	blood:
27	chr4:10254361..10256671-chr4:10262474..10264248,2	K562	blood:
28	chr4:10300976..10303713-chr4:10304138..10305960,3	K562	blood:
29	chr4:10283364..10286619-chr4:10288507..10291288,3	K562	blood:
30	chr4:10250648..10253943-chr4:10254760..10258340,4	K562	blood:
31	chr4:10320256..10323019-chr4:10334627..10337093,2	K562	blood:
32	chr4:10346990..10348791-chr4:10349503..10352332,2	K562	blood:
33	chr4:10181898..10186356-chr4:10317430..10320755,4	K562	blood:
34	chr4:10117842..10119536-chr4:10257217..10259311,2	K562	blood:
35	chr4:10288926..10293598-chr4:10293770..10299284,5	K562	blood:
36	chr4:10278587..10280479-chr4:10297418..10299087,2	K562	blood:
37	chr4:10117355..10119664-chr4:10257217..10260454,4	K562	blood:
38	chr4:10349621..10351967-chr4:10356635..10358807,2	K562	blood:
39	chr4:10257186..10261463-chr4:10263373..10268480,7	K562	blood:
40	chr4:10274788..10276860-chr4:10285063..10286717,2	K562	blood:
41	chr4:10344224..10346031-chr4:10349047..10351434,2	K562	blood:
42	chr4:10326438..10329327-chr4:10340874..10342507,2	K562	blood:
43	chr4:10331837..10333791-chr4:10338261..10340215,2	K562	blood:
44	chr4:10346965..10350105-chr4:10350832..10355022,4	K562	blood:
45	chr4:10271663..10276718-chr4:10277557..10282432,8	K562	blood:
46	chr4:10236259..10238046-chr4:10240029..10241603,2	K562	blood:
47	chr4:10327845..10330613-chr4:10374388..10375996,2	K562	blood:
48	chr4:10305228..10307997-chr4:10310331..10312718,2	K562	blood:
49	chr4:10249783..10252189-chr4:10254326..10257178,3	K562	blood:
50	chr4:10361812..10363629-chr4:10366442..10368380,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF518B-2	chr4:10293819-10294332	NONHSAT095494
2	lnc-DRD5-18	chr4:10359894-10360314	l_2604_chr4:10348296-10419642_testes
3	lnc-WDR1-10	chr4:10261069-10261762	NONHSAT095491
4	lnc-DRD5-18	chr4:10348297-10348499	l_2604_chr4:10348296-10419642_testes
5	lnc-DRD5-18	chr4:10348828-10349271	l_2604_chr4:10348296-10419642_testes
6	lnc-WDR1-11	chr4:10269519-10269855	NONHSAT095492
7	lnc-ZNF518B-3	chr4:10286585-10287332	NONHSAT095493
8	lnc-DRD5-18	chr4:10352660-10352812	l_2604_chr4:10348296-10419642_testes
9	lnc-WDR1-9	chr4:10256550-10258245	NONHSAT095490

No data

Variant related genes	Relation type
ENSG00000251338	TF binding region
ENSG00000271544	TF binding region
ENSG00000250040	TF binding region
ENSG00000250074	TF binding region
ENSG00000251278	TF binding region
ENSG00000250573	TF binding region
ENSG00000250505	TF binding region
ENSG00000251338	CpG island
ENSG00000271544	CpG island
ENSG00000250040	CpG island
ENSG00000250074	CpG island
ENSG00000251278	CpG island
ENSG00000250573	CpG island
ENSG00000250505	CpG island
ENSG00000223086	chromatin interactions
ENSG00000251296	chromatin interactions
ENSG00000271544	chromatin interactions
ENSG00000250573	chromatin interactions
ENSG00000251278	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000250040	chromatin interactions
ENSG00000251338	chromatin interactions
ENSG00000178163	chromatin interactions

Extended variants
information (count: 8575 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:8575 , 50 per page) page: 1 2 3 4 5 6 7 ... 172

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553694403	chr4:10230024-10230025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs146088694	chr4:10230042-10230043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138870452	chr4:10230095-10230096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554388310	chr4:10230114-10230115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs13128285	chr4:10230132-10230133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs13144578	chr4:10230133-10230134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372600023	chr4:10230229-10230230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190618773	chr4:10230249-10230250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543170764	chr4:10230271-10230272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562842767	chr4:10230285-10230286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376425616	chr4:10230306-10230307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141715309	chr4:10230337-10230338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs58661929	chr4:10230367-10230368	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs115367830	chr4:10230380-10230381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181869360	chr4:10230387-10230388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528040790	chr4:10230408-10230409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs115802237	chr4:10230409-10230410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76026697	chr4:10230430-10230431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs55834068	chr4:10230434-10230435	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs550321130	chr4:10230485-10230486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185212913	chr4:10230504-10230505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538712263	chr4:10230514-10230515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73808656	chr4:10230550-10230551	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs189888177	chr4:10230616-10230617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530527486	chr4:10230729-10230730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs148464516	chr4:10230730-10230731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs1004696	chr4:10230756-10230757	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs571767027	chr4:10230808-10230809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs80355356	chr4:10230885-10230886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575883081	chr4:10230942-10230943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181257564	chr4:10230944-10230945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185315061	chr4:10230989-10230990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74526970	chr4:10230990-10230991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189728886	chr4:10231019-10231020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2110024	chr4:10231033-10231034	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs547835072	chr4:10231075-10231076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560327804	chr4:10231081-10231082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539246599	chr4:10231137-10231138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs56845179	chr4:10231168-10231169	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs142670539	chr4:10231230-10231231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs56682364	chr4:10231237-10231238	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs150601854	chr4:10231323-10231324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1158093	chr4:10231324-10231325	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs565454311	chr4:10231343-10231344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532154012	chr4:10231407-10231408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139458854	chr4:10231432-10231433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76947294	chr4:10231459-10231460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149669459	chr4:10231474-10231475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535847091	chr4:10231494-10231495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs114099547	chr4:10231496-10231497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:461 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10223400-10233800	Weak transcription	K562	blood
2	chr4:10233400-10234600	Enhancers	Rectal Smooth Muscle	rectum
3	chr4:10233800-10234600	Enhancers	K562	blood
4	chr4:10234600-10236400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:10234600-10238600	Weak transcription	K562	blood
6	chr4:10238000-10257000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr4:10238600-10241800	Enhancers	K562	blood
8	chr4:10239800-10244200	Enhancers	HSMMtube	muscle
9	chr4:10240600-10243600	Enhancers	Fetal Heart	heart
10	chr4:10241000-10241400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:10241200-10243000	Enhancers	Fetal Stomach	stomach
12	chr4:10241400-10242000	Enhancers	Brain Hippocampus Middle	brain
13	chr4:10241800-10242200	Flanking Active TSS	K562	blood
14	chr4:10241800-10242800	Enhancers	Fetal Muscle Leg	muscle
15	chr4:10242000-10242600	Enhancers	Left Ventricle	heart
16	chr4:10242200-10246200	Enhancers	K562	blood
17	chr4:10242400-10242800	Enhancers	Fetal Lung	lung
18	chr4:10243600-10246200	Weak transcription	Fetal Heart	heart
19	chr4:10244000-10255400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr4:10246200-10246600	Weak transcription	K562	blood
21	chr4:10246400-10246600	Enhancers	Fetal Heart	heart
22	chr4:10246600-10248200	Enhancers	K562	blood
23	chr4:10246800-10248200	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr4:10247000-10247200	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr4:10247200-10247400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
26	chr4:10247400-10247800	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr4:10247800-10248000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
28	chr4:10248200-10256800	Weak transcription	K562	blood
29	chr4:10254800-10257200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr4:10255000-10255200	Enhancers	Fetal Thymus	thymus
31	chr4:10255000-10256400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr4:10255000-10256600	Enhancers	NHEK	skin
33	chr4:10255200-10256400	Enhancers	HMEC	breast
34	chr4:10255400-10256000	Weak transcription	Fetal Thymus	thymus
35	chr4:10255400-10256400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr4:10256000-10256200	Enhancers	Fetal Thymus	thymus
37	chr4:10256200-10261800	Weak transcription	Fetal Thymus	thymus
38	chr4:10256400-10261600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr4:10256400-10261800	Weak transcription	HMEC	breast
40	chr4:10256600-10261200	Weak transcription	NHEK	skin
41	chr4:10256800-10257000	Enhancers	K562	blood
42	chr4:10257000-10257400	Weak transcription	K562	blood
43	chr4:10257000-10257600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr4:10257200-10261200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr4:10257400-10258800	Enhancers	K562	blood
46	chr4:10257600-10262400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr4:10258800-10261200	Weak transcription	K562	blood
48	chr4:10259800-10260600	Enhancers	Fetal Heart	heart
49	chr4:10261200-10262000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr4:10261200-10262200	Enhancers	NHEK	skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links