Variant report

Variant	nsv1007053
Chromosome Location	chr4:22573534-22658117
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:497)
CpG islands
(count:793)
Chromatin interactive
region (count:7)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:497 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:22597318-22597734	GM12878	blood:	n/a	n/a
2	ATF2	chr4:22632891-22633274	GM12878	blood:	n/a	n/a
3	BATF	chr4:22606760-22606960	GM12878	blood:	n/a	n/a
4	BATF	chr4:22601520-22601932	GM12878	blood:	n/a	n/a
5	BATF	chr4:22632911-22633232	GM12878	blood:	n/a	n/a
6	BATF	chr4:22601547-22601922	GM12878	blood:	n/a	n/a
7	BATF	chr4:22597407-22597668	GM12878	blood:	n/a	n/a
8	BATF	chr4:22597162-22597792	GM12878	blood:	n/a	n/a
9	BCL11A	chr4:22632894-22633130	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:22597323-22597768	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:22597442-22597626	GM12878	blood:	n/a	n/a
12	BCL3	chr4:22656969-22657254	GM12878	blood:	n/a	n/a
13	BCLAF1	chr4:22597480-22597752	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:22596931-22597736	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:22632892-22633436	GM12878	blood:	n/a	n/a
16	CEBPB	chr4:22621829-22622059	A549	lung:	n/a	chr4:22621972-22621983
17	CEBPB	chr4:22621846-22622104	IMR90	lung:	n/a	chr4:22621972-22621983
18	CEBPB	chr4:22621971-22622103	H1-hESC	embryonic stem cell:	n/a	chr4:22621972-22621983
19	CEBPB	chr4:22611997-22612347	HepG2	liver:	n/a	chr4:22612176-22612187
20	CEBPB	chr4:22657749-22657936	H1-hESC	embryonic stem cell:	n/a	chr4:22657835-22657846
21	CEBPB	chr4:22621914-22622114	Hela-S3	cervix:	n/a	chr4:22621972-22621983
22	CEBPB	chr4:22621795-22622157	HepG2	liver:	n/a	chr4:22621972-22621983
23	CEBPB	chr4:22621924-22622029	HepG2	liver:	n/a	chr4:22621972-22621983
24	CEBPB	chr4:22657671-22658002	IMR90	lung:	n/a	chr4:22657835-22657846
25	CEBPB	chr4:22657679-22658007	HepG2	liver:	n/a	chr4:22657835-22657846
26	CEBPB	chr4:22612041-22612267	IMR90	lung:	n/a	chr4:22612176-22612187
27	CEBPB	chr4:22581187-22581490	HepG2	liver:	n/a	chr4:22581339-22581350
28	CEBPB	chr4:22612053-22612350	Hela-S3	cervix:	n/a	chr4:22612176-22612187
29	CEBPB	chr4:22612043-22612286	A549	lung:	n/a	chr4:22612176-22612187
30	CEBPB	chr4:22581249-22581454	A549	lung:	n/a	chr4:22581339-22581350
31	CEBPB	chr4:22634675-22634896	HepG2	liver:	n/a	chr4:22634777-22634788
32	CEBPB	chr4:22657722-22657962	A549	lung:	n/a	chr4:22657835-22657846
33	CEBPB	chr4:22581213-22581427	IMR90	lung:	n/a	chr4:22581339-22581350
34	CHD1	chr4:22597008-22597194	GM12878	blood:	n/a	n/a
35	CHD1	chr4:22597526-22597852	GM12878	blood:	n/a	n/a
36	CHD2	chr4:22609035-22609302	GM12878	blood:	n/a	n/a
37	CHD2	chr4:22601347-22601539	GM12878	blood:	n/a	n/a
38	CHD2	chr4:22597442-22597719	GM12878	blood:	n/a	n/a
39	CHD2	chr4:22608992-22609179	HepG2	liver:	n/a	n/a
40	CTCF	chr4:22609012-22609293	ECC-1	luminal epithelium:	n/a	n/a
41	CTCF	chr4:22609100-22609250	HCT-116	colon:	n/a	n/a
42	CTCF	chr4:22637460-22637610	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:22609080-22609230	GM12875	blood:	n/a	n/a
44	CTCF	chr4:22609060-22609210	A549	lung:	n/a	n/a
45	CTCF	chr4:22609018-22609301	MCF-7	breast:	n/a	n/a
46	CTCF	chr4:22609080-22609230	HVMF	connective:	n/a	n/a
47	CTCF	chr4:22609040-22609286	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr4:22576140-22576290	SK-N-SH_RA	brain:	n/a	chr4:22576245-22576263 chr4:22576247-22576268
49	CTCF	chr4:22637400-22637550	HEK293	kidney:	n/a	n/a
50	CTCF	chr4:22608959-22609339	IMR90	lung:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:22590647-22590697	ovcar-3	ovarian:	n/a
2	chr4:22623333-22623383	SKMC	muscle:	n/a
3	chr4:22623333-22623383	HCPEpiC	choroid plexus:	n/a
4	chr4:22636203-22636253	HMEC	breast:	n/a
5	chr4:22623252-22623302	SAEC	small airway:	n/a
6	chr4:22636392-22636442	HEK293	kidney:	embryo
7	chr4:22588665-22588715	HEEpiC	esophagus:	n/a
8	chr4:22588245-22588295	HCPEpiC	choroid plexus:	n/a
9	chr4:22588665-22588715	HCM	heart:	n/a
10	chr4:22636672-22636722	HL-60	blood:	n/a
11	chr4:22636672-22636722	H1-hESC	embryonic stem cell:	embryo
12	chr4:22590175-22590225	Caco-2	colon:	n/a
13	chr4:22636392-22636442	NH-A	brain:	n/a
14	chr4:22623333-22623383	GM06990	blood:	n/a
15	chr4:22636672-22636722	CMK	blood:	n/a
16	chr4:22588245-22588295	PANC-1	pancreas:	n/a
17	chr4:22588208-22588258	AG10803	skin:	n/a
18	chr4:22588658-22588708	SKMC	muscle:	n/a
19	chr4:22636203-22636253	HPAEpiC	pulmonary alveolar:	n/a
20	chr4:22590647-22590697	GM12892	blood:	n/a
21	chr4:22623367-22623417	HCT-116	colon:	n/a
22	chr4:22623333-22623383	SK-N-SH	brain:	n/a
23	chr4:22588658-22588708	ProgFib	skin:	n/a
24	chr4:22590411-22590461	NB4	blood:	n/a
25	chr4:22588665-22588715	NHDF-neo	bronchial:	n/a
26	chr4:22590175-22590225	HMEC	breast:	n/a
27	chr4:22590647-22590697	LNCaP	prostate:	n/a
28	chr4:22623367-22623417	HUVEC	blood vessel:	n/a
29	chr4:22623367-22623417	BJ	skin:	n/a
30	chr4:22623252-22623302	Hela-S3	cervix:	n/a
31	chr4:22636203-22636253	AG09309	skin:	n/a
32	chr4:22588245-22588295	HEEpiC	esophagus:	n/a
33	chr4:22588658-22588708	PFSK-1	brain:	n/a
34	chr4:22636392-22636442	AG09309	skin:	n/a
35	chr4:22588245-22588295	U87	brain:	n/a
36	chr4:22623333-22623383	HMEC	breast:	n/a
37	chr4:22590175-22590225	PFSK-1	brain:	n/a
38	chr4:22590175-22590225	CMK	blood:	n/a
39	chr4:22590647-22590697	NH-A	brain:	n/a
40	chr4:22623333-22623383	SK-N-SH_RA	brain:	n/a
41	chr4:22590175-22590225	BE2_C	brain:	n/a
42	chr4:22623367-22623417	MCF-7	breast:	n/a
43	chr4:22590411-22590461	K562	blood:	n/a
44	chr4:22636392-22636442	NB4	blood:	n/a
45	chr4:22636392-22636442	MCF-7	breast:	n/a
46	chr4:22623367-22623417	AG10803	skin:	n/a
47	chr4:22588658-22588708	AG04450	lung:	fetal
48	chr4:22590647-22590697	RPTEC	kidney:	n/a
49	chr4:22623252-22623302	HepG2	liver:	n/a
50	chr4:22623367-22623417	Hepatocyte	liver:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:22645860..22647619-chr4:22652276..22653871,2	K562	blood:
2	chr4:22642022..22643894-chr4:22646674..22649581,2	K562	blood:
3	chr4:22575405..22577612-chr4:22584979..22587113,2	MCF-7	breast:
4	chr4:22575405..22577612-chr4:22584979..22587113,2	MCF-7	breast:
5	chr4:22642022..22643894-chr4:22646674..22649581,2	K562	blood:
6	chr18:24510025..24511017-chr4:22608413..22609080,2	MCF-7	breast:
7	chr4:22645860..22647619-chr4:22652276..22653871,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PACRGL-12	chr4:22608315-22608334	l_2614_chr4:22608314-22651921_testes
2	lnc-PACRGL-12	chr4:22608272-22608334	ucscGeneNc_uc003gqr_1
3	lnc-PACRGL-10	chr4:22611966-22612076	NONHSAT095765
4	lnc-PACRGL-10	chr4:22611344-22611472	NONHSAT095765
5	lnc-PACRGL-12	chr4:22613871-22613964	ucscGeneNc_uc003gqr_1
6	lnc-PACRGL-12	chr4:22610306-22610433	l_2614_chr4:22608314-22651921_testes
7	lnc-PACRGL-12	chr4:22613866-22613964	l_2614_chr4:22608314-22651921_testes
8	lnc-PACRGL-10	chr4:22612601-22612686	NONHSAT095765
9	lnc-PACRGL-9	chr4:22595819-22596073	NONHSAT095763
10	lnc-PACRGL-12	chr4:22651411-22651921	l_2614_chr4:22608314-22651921_testes
11	lnc-PACRGL-12	chr4:22610306-22610433	ucscGeneNc_uc003gqr_1
12	lnc-PACRGL-10	chr4:22609124-22609169	NONHSAT095765

No data

Variant related genes	Relation type
ENSG00000244538	TF binding region
ENSG00000251516	TF binding region
ENSG00000244538	CpG island
ENSG00000251516	CpG island

Extended variants
information (count: 2036 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2036 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145973386	chr4:22573547-22573548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs192285689	chr4:22573583-22573584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572463259	chr4:22573593-22573594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs34268046	chr4:22573717-22573718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201298107	chr4:22573742-22573743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7690673	chr4:22573761-22573762	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs563942429	chr4:22573784-22573785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs13118243	chr4:22573800-22573801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs72099496	chr4:22573803-22573804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531461096	chr4:22573812-22573813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139839680	chr4:22573819-22573820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183224678	chr4:22573824-22573825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143397416	chr4:22573844-22573845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34880876	chr4:22573858-22573859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs28579069	chr4:22573880-22573881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs111999082	chr4:22573881-22573882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs28415161	chr4:22573882-22573883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373617113	chr4:22573883-22573884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187945634	chr4:22573884-22573885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs71182950	chr4:22573894-22573895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547110632	chr4:22573962-22573963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191308349	chr4:22574026-22574027	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533079252	chr4:22574038-22574039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10031013	chr4:22574049-22574050	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs571051088	chr4:22574067-22574068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538489287	chr4:22574104-22574105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370536558	chr4:22574157-22574158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368986421	chr4:22574166-22574167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568695011	chr4:22574196-22574197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535808567	chr4:22574209-22574210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553900929	chr4:22574236-22574237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549653412	chr4:22574300-22574301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569684220	chr4:22574303-22574304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572457372	chr4:22574306-22574307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182382148	chr4:22574329-22574330	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146715195	chr4:22574425-22574426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs76036482	chr4:22574449-22574450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543240566	chr4:22574471-22574472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs73247158	chr4:22574476-22574477	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs529188858	chr4:22574478-22574479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150263683	chr4:22574506-22574507	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540992419	chr4:22574550-22574551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188190463	chr4:22574639-22574640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116664105	chr4:22574642-22574643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114483970	chr4:22574650-22574651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192784270	chr4:22574721-22574722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139138129	chr4:22574762-22574763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs73247159	chr4:22574774-22574775	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs34129326	chr4:22574780-22574781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs137883186	chr4:22574848-22574849	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Cancer	22183965	CNVD
Gastric cancer	16891809	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:189 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:22573400-22573600	Enhancers	Fetal Muscle Leg	muscle
2	chr4:22573400-22574000	Weak transcription	Colon Smooth Muscle	Colon
3	chr4:22573600-22575000	Weak transcription	Fetal Muscle Leg	muscle
4	chr4:22574000-22577800	Enhancers	Colon Smooth Muscle	Colon
5	chr4:22574400-22574600	Enhancers	Brain Anterior Caudate	brain
6	chr4:22574400-22574600	Enhancers	Fetal Lung	lung
7	chr4:22574400-22575200	Enhancers	Brain Germinal Matrix	brain
8	chr4:22574400-22575200	Enhancers	Fetal Stomach	stomach
9	chr4:22574400-22575600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr4:22574400-22575800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr4:22574400-22576400	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr4:22574400-22576800	Enhancers	Rectal Smooth Muscle	rectum
13	chr4:22574400-22577000	Enhancers	Fetal Heart	heart
14	chr4:22574600-22575200	Weak transcription	Fetal Lung	lung
15	chr4:22574600-22575600	Weak transcription	Brain Anterior Caudate	brain
16	chr4:22574800-22575200	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr4:22574800-22575600	Enhancers	HSMMtube	muscle
18	chr4:22575000-22575200	Enhancers	Small Intestine	intestine
19	chr4:22575000-22575600	Enhancers	Fetal Muscle Leg	muscle
20	chr4:22575000-22575600	Enhancers	Psoas Muscle	Psoas
21	chr4:22575200-22575800	Enhancers	Fetal Lung	lung
22	chr4:22575200-22576200	Weak transcription	Brain Germinal Matrix	brain
23	chr4:22575400-22575600	Enhancers	Stomach Smooth Muscle	stomach
24	chr4:22575600-22576000	Enhancers	Brain Anterior Caudate	brain
25	chr4:22576200-22576400	Enhancers	Brain Germinal Matrix	brain
26	chr4:22576800-22579000	Weak transcription	Rectal Smooth Muscle	rectum
27	chr4:22577800-22579600	Weak transcription	Colon Smooth Muscle	Colon
28	chr4:22579000-22579200	Enhancers	Rectal Smooth Muscle	rectum
29	chr4:22579200-22579600	Weak transcription	Rectal Smooth Muscle	rectum
30	chr4:22579600-22580400	Enhancers	Colon Smooth Muscle	Colon
31	chr4:22579600-22580400	Enhancers	Rectal Smooth Muscle	rectum
32	chr4:22580000-22580400	Enhancers	Liver	Liver
33	chr4:22595400-22596200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr4:22596600-22599400	Enhancers	Fetal Heart	heart
35	chr4:22596800-22597600	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr4:22596800-22600000	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr4:22596800-22600000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr4:22597000-22597600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr4:22597200-22597400	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr4:22597400-22597800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
41	chr4:22597600-22598200	Enhancers	HSMMtube	muscle
42	chr4:22597600-22598800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr4:22597600-22600000	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr4:22597600-22600200	Enhancers	Primary hematopoietic stem cells	blood
45	chr4:22597800-22598400	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr4:22598000-22598200	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr4:22598400-22598600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
48	chr4:22598400-22599200	Enhancers	Fetal Lung	lung
49	chr4:22598600-22599000	Active TSS	Monocytes-CD14+_RO01746	blood
50	chr4:22598800-22599000	Enhancers	Rectal Mucosa Donor 31	rectum

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