Variant report

Variant	nsv1025720
Chromosome Location	chr7:5853557-5934780
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1254)
CpG islands
(count:1709)
Chromatin interactive
region (count:12)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1254 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:5867592-5867694	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:5867459-5867694	K562	blood:	n/a	n/a
3	ARID3A	chr7:5908686-5908892	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:5862273-5862605	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:5862528-5862814	K562	blood:	n/a	n/a
6	ATF1	chr7:5862457-5862892	K562	blood:	n/a	n/a
7	ATF2	chr7:5862330-5862768	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr7:5862327-5862966	GM12878	blood:	n/a	n/a
9	ATF2	chr7:5862355-5862904	GM12878	blood:	n/a	n/a
10	ATF2	chr7:5862306-5862777	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr7:5862635-5862799	GM12878	blood:	n/a	n/a
12	ATF3	chr7:5862558-5862865	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr7:5862563-5862853	HepG2	liver:	n/a	n/a
14	ATF3	chr7:5862421-5862902	HepG2	liver:	n/a	n/a
15	ATF3	chr7:5862384-5862926	GM12878	blood:	n/a	n/a
16	ATF3	chr7:5862411-5862898	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr7:5862540-5862867	K562	blood:	n/a	n/a
18	BATF	chr7:5896136-5896348	GM12878	blood:	n/a	n/a
19	BCLAF1	chr7:5896165-5896407	GM12878	blood:	n/a	n/a
20	BCLAF1	chr7:5862267-5862957	GM12878	blood:	n/a	n/a
21	BHLHE40	chr7:5862470-5862879	HepG2	liver:	n/a	n/a
22	BHLHE40	chr7:5862309-5862995	GM12878	blood:	n/a	n/a
23	BHLHE40	chr7:5896140-5896326	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:5862350-5862941	K562	blood:	n/a	n/a
25	BHLHE40	chr7:5889190-5889204	K562	blood:	n/a	n/a
26	BRCA1	chr7:5896176-5896337	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr7:5862392-5862880	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr7:5862294-5862858	K562	blood:	n/a	n/a
29	CBX3	chr7:5862122-5862937	K562	blood:	n/a	n/a
30	CCNT2	chr7:5862562-5862965	K562	blood:	n/a	n/a
31	CEBPB	chr7:5892975-5893174	A549	lung:	n/a	chr7:5893027-5893038
32	CEBPB	chr7:5862485-5862785	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr7:5896180-5896389	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr7:5890492-5890732	K562	blood:	n/a	chr7:5890571-5890582
35	CEBPB	chr7:5892913-5893127	H1-hESC	embryonic stem cell:	n/a	chr7:5893027-5893038
36	CEBPB	chr7:5891809-5891870	IMR90	lung:	n/a	n/a
37	CEBPB	chr7:5890537-5890656	IMR90	lung:	n/a	chr7:5890571-5890582
38	CEBPB	chr7:5890460-5890688	HepG2	liver:	n/a	chr7:5890571-5890582
39	CEBPB	chr7:5862300-5862905	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr7:5862463-5862811	K562	blood:	n/a	n/a
41	CEBPB	chr7:5891846-5891857	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr7:5893018-5893091	Hela-S3	cervix:	n/a	chr7:5893027-5893038
43	CEBPB	chr7:5929893-5930182	K562	blood:	n/a	n/a
44	CEBPB	chr7:5890537-5890700	A549	lung:	n/a	chr7:5890571-5890582
45	CEBPB	chr7:5892955-5893172	K562	blood:	n/a	chr7:5893027-5893038
46	CEBPB	chr7:5892975-5893180	HepG2	liver:	n/a	chr7:5893027-5893038
47	CEBPB	chr7:5857273-5857447	K562	blood:	n/a	n/a
48	CEBPB	chr7:5890535-5890604	H1-hESC	embryonic stem cell:	n/a	chr7:5890571-5890582
49	CEBPB	chr7:5912087-5912368	IMR90	lung:	n/a	n/a
50	CEBPB	chr7:5929312-5929450	IMR90	lung:	n/a	n/a

(count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5911900-5911950	AG09319	gingival:	n/a
2	chr7:5911900-5911950	AG09319	gingival:	n/a
3	chr7:5911701-5911751	GM12891	blood:	n/a
4	chr7:5862740-5862790	NHDF-neo	bronchial:	n/a
5	chr7:5919589-5919639	GM19239	blood:	n/a
6	chr7:5862740-5862790	GM12878	blood:	n/a
7	chr7:5888077-5888127	RPTEC	kidney:	n/a
8	chr7:5862740-5862790	AG09309	skin:	n/a
9	chr7:5863813-5863863	LNCaP	prostate:	n/a
10	chr7:5887023-5887073	IMR90	lung:	fetal
11	chr7:5863813-5863863	MCF-7	breast:	n/a
12	chr7:5911800-5911850	HEK293	kidney:	embryo
13	chr7:5862449-5862499	SK-N-MC	brain:	n/a
14	chr7:5920535-5920585	HEEpiC	esophagus:	n/a
15	chr7:5919589-5919639	A549	lung:	n/a
16	chr7:5863813-5863863	SK-N-SH_RA	brain:	n/a
17	chr7:5863510-5863560	AG09309	skin:	n/a
18	chr7:5887023-5887073	AG09309	skin:	n/a
19	chr7:5920635-5920685	HRCEpiC	kidney:	n/a
20	chr7:5859245-5859295	MCF-7	breast:	n/a
21	chr7:5886722-5886772	HIPEpiC	eye:	n/a
22	chr7:5919583-5919633	HAEpiC	amniotic membrane:	n/a
23	chr7:5862839-5862889	U87	brain:	n/a
24	chr7:5885244-5885294	T-47D	breast:	n/a
25	chr7:5862658-5862708	CMK	blood:	n/a
26	chr7:5862449-5862499	HCPEpiC	choroid plexus:	n/a
27	chr7:5863813-5863863	HCT-116	colon:	n/a
28	chr7:5885244-5885294	HCM	heart:	n/a
29	chr7:5911800-5911850	HL-60	blood:	n/a
30	chr7:5859245-5859295	BE2_C	brain:	n/a
31	chr7:5862839-5862889	MCF10A-Er-Src	breast:	n/a
32	chr7:5919012-5919062	SK-N-MC	brain:	n/a
33	chr7:5862449-5862499	HPAEpiC	pulmonary alveolar:	n/a
34	chr7:5862996-5863046	HL-60	blood:	n/a
35	chr7:5862451-5862501	GM12891	blood:	n/a
36	chr7:5865915-5865965	HPAEpiC	pulmonary alveolar:	n/a
37	chr7:5862658-5862708	HCF	heart:	n/a
38	chr7:5862449-5862499	HRE	kidney:	n/a
39	chr7:5911800-5911850	LNCaP	prostate:	n/a
40	chr7:5919583-5919633	AG09309	skin:	n/a
41	chr7:5920635-5920685	HepG2	liver:	n/a
42	chr7:5883645-5883695	AG09309	skin:	n/a
43	chr7:5863813-5863863	ovcar-3	ovarian:	n/a
44	chr7:5863813-5863863	RPTEC	kidney:	n/a
45	chr7:5865915-5865965	GM12892	blood:	n/a
46	chr7:5919589-5919639	AG09309	skin:	n/a
47	chr7:5862609-5862659	HRCEpiC	kidney:	n/a
48	chr7:5887023-5887073	GM12891	blood:	n/a
49	chr7:5862983-5863033	HCT-116	colon:	n/a
50	chr7:5911800-5911850	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:5921888..5923776-chr7:6615172..6617060,2	K562	blood:
2	chr7:5877107..5878733-chr7:5880762..5883645,2	K562	blood:
3	chr7:5877107..5878733-chr7:5880762..5883645,2	K562	blood:
4	chr3:107149613..107150322-chr7:5862636..5863385,2	NB4	blood:
5	chr7:5896217..5898583-chr7:97641356..97642858,2	MCF-7	breast:
6	chr7:5875724..5878623-chr7:5880700..5882793,2	MCF-7	breast:
7	chr7:5875724..5878623-chr7:5880700..5882793,2	MCF-7	breast:
8	chr7:5464152..5466960-chr7:5862123..5864390,2	MCF-7	breast:
9	chr7:5866466..5869217-chr7:5871734..5873608,2	MCF-7	breast:
10	chr7:5895754..5896691-chr7:6036473..6037181,2	MCF-7	breast:
11	chr7:5877192..5879014-chr7:6172405..6175361,2	K562	blood:
12	chr7:5866466..5869217-chr7:5871734..5873608,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCM-3	chr7:5873158-5873199	NONHSAT118942
2	lnc-RSPH10B-1	chr7:5911384-5911681	NONHSAT118956
3	lnc-OCM-3	chr7:5873158-5873199	NONHSAT118948
4	lnc-OCM-3	chr7:5862875-5863157	NONHSAT118948
5	lnc-OCM-1	chr7:5855829-5855979	XLOC_005976
6	lnc-OCM-3	chr7:5862823-5863157	NONHSAT118944
7	lnc-OCM-3	chr7:5862820-5863157	NONHSAT118942
8	lnc-OCM-3	chr7:5870812-5870914	NONHSAT118942
9	lnc-OCM-1	chr7:5855828-5855979	NONHSAT118937
10	lnc-OCM-3	chr7:5880321-5880487	NONHSAT118944
11	lnc-OCM-3	chr7:5873158-5873199	NONHSAT118944
12	lnc-OCM-3	chr7:5879580-5879706	NONHSAT118944
13	lnc-OCM-3	chr7:5893738-5893857	NONHSAT118944
14	lnc-OCM-3	chr7:5878820-5878850	NONHSAT118948
15	lnc-OCM-3	chr7:5878701-5878783	NONHSAT118942

No data

Variant related genes	Relation type
CCZ1	TF binding region
OCM	TF binding region
ZNF815P	TF binding region
RN7SL556P	TF binding region
CCZ1	CpG island
OCM	CpG island
ZNF815P	CpG island
RN7SL556P	CpG island
ENSG00000273125	chromatin interactions
ENSG00000272953	chromatin interactions
ENSG00000182095	chromatin interactions

Extended variants
information (count: 4805 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4805 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572823128	chr7:5855835-5855836	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs144026691	chr7:5855836-5855837	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs564852559	chr7:5855853-5855854	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs191472703	chr7:5855861-5855862	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs544507772	chr7:5855863-5855864	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs183333592	chr7:5855871-5855872	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs527987867	chr7:5855878-5855879	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs548050944	chr7:5855893-5855894	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs370703628	chr7:5855909-5855910	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs566969233	chr7:5855950-5855951	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs527766124	chr7:5855952-5855953	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs552571868	chr7:5855971-5855972	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs186871361	chr7:5858201-5858202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562939608	chr7:5858202-5858203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530750292	chr7:5858204-5858205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552825306	chr7:5858211-5858212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140944839	chr7:5858232-5858233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561522396	chr7:5858263-5858264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534842769	chr7:5858267-5858268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546784743	chr7:5858287-5858288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191280616	chr7:5858302-5858303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs62455919	chr7:5858319-5858320	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs147960281	chr7:5858325-5858326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1964283	chr7:5858336-5858337	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs532050358	chr7:5858344-5858345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184176644	chr7:5858353-5858354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573422668	chr7:5858362-5858363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150415303	chr7:5858395-5858396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565113641	chr7:5858397-5858398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577362194	chr7:5858398-5858399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562081091	chr7:5858412-5858413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544692084	chr7:5858424-5858425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34399026	chr7:5858459-5858460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529305069	chr7:5858513-5858514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529195481	chr7:5858515-5858516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145236543	chr7:5858539-5858540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149174374	chr7:5858570-5858571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561253691	chr7:5858601-5858602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs28421113	chr7:5858607-5858608	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs546846001	chr7:5858628-5858629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548669038	chr7:5858639-5858640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370863903	chr7:5858640-5858641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188699777	chr7:5858654-5858655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532694772	chr7:5858658-5858659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs193203629	chr7:5858661-5858662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566089668	chr7:5858668-5858669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569225130	chr7:5858672-5858673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143297054	chr7:5858679-5858680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554649206	chr7:5858709-5858710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533140344	chr7:5858733-5858734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Schizophrenia	21346763	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:946 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5858200-5862000	Weak transcription	K562	blood
2	chr7:5859400-5860000	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr7:5859400-5860200	Enhancers	Primary hematopoietic stem cells	blood
4	chr7:5859400-5861400	Enhancers	HUVEC	blood vessel
5	chr7:5859600-5860000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr7:5859600-5860000	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr7:5859600-5860800	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr7:5859600-5862200	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr7:5859800-5861200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr7:5860000-5860200	Enhancers	Primary B cells from cord blood	blood
11	chr7:5860000-5860200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:5860000-5860200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
13	chr7:5860000-5861200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
14	chr7:5860200-5860400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:5860200-5860600	Active TSS	Monocytes-CD14+_RO01746	blood
16	chr7:5860200-5862000	Weak transcription	Primary hematopoietic stem cells	blood
17	chr7:5860400-5860600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr7:5860600-5860800	Enhancers	Fetal Muscle Trunk	muscle
19	chr7:5860600-5861000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr7:5860600-5861000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
21	chr7:5860800-5861000	Enhancers	Primary B cells from peripheral blood	blood
22	chr7:5860800-5861000	Enhancers	Fetal Thymus	thymus
23	chr7:5860800-5862000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr7:5861000-5861400	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr7:5861000-5862000	Weak transcription	Primary B cells from peripheral blood	blood
26	chr7:5861000-5862000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr7:5861000-5862000	Weak transcription	Fetal Muscle Trunk	muscle
28	chr7:5861000-5862000	Weak transcription	Fetal Thymus	thymus
29	chr7:5861200-5861600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr7:5861200-5862000	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr7:5861400-5861800	Weak transcription	HUVEC	blood vessel
32	chr7:5861400-5861800	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr7:5861600-5862200	Enhancers	Primary T cells fromperipheralblood	blood
34	chr7:5861600-5862200	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr7:5861600-5862200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr7:5861800-5862000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr7:5861800-5862000	Enhancers	Lung	lung
38	chr7:5861800-5862000	Enhancers	A549	lung
39	chr7:5861800-5862000	Enhancers	Dnd41	blood
40	chr7:5861800-5862000	Enhancers	GM12878-XiMat	blood
41	chr7:5861800-5862000	Enhancers	Hela-S3	cervix
42	chr7:5861800-5862000	Enhancers	HepG2	liver
43	chr7:5861800-5862000	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr7:5861800-5862200	Enhancers	Primary B cells from cord blood	blood
45	chr7:5861800-5862200	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr7:5861800-5862200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr7:5861800-5862200	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr7:5861800-5862200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr7:5861800-5862200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr7:5861800-5862200	Enhancers	Primary T killer memory cells from peripheral blood	blood

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