Variant report

Variant	nsv889236
Chromosome Location	chr7:135884571-135943264
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:168)
CpG islands
(count:61)
Chromatin interactive
region (count:31)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:168 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:135931947-135932309	K562	blood:	n/a	n/a
2	ARID3A	chr7:135930122-135930423	K562	blood:	n/a	n/a
3	ATF1	chr7:135931923-135932438	K562	blood:	n/a	n/a
4	ATF1	chr7:135930049-135930441	K562	blood:	n/a	n/a
5	BCL11A	chr7:135914982-135915190	GM12878	blood:	n/a	chr7:135915177-135915186
6	BHLHE40	chr7:135930104-135930326	K562	blood:	n/a	n/a
7	CBX3	chr7:135929972-135930428	K562	blood:	n/a	n/a
8	CBX3	chr7:135920838-135921270	K562	blood:	n/a	n/a
9	CBX3	chr7:135938899-135939272	K562	blood:	n/a	n/a
10	CBX3	chr7:135929954-135930521	K562	blood:	n/a	n/a
11	CBX3	chr7:135916100-135916470	K562	blood:	n/a	n/a
12	CCNT2	chr7:135934694-135934784	K562	blood:	n/a	n/a
13	CCNT2	chr7:135925380-135925574	K562	blood:	n/a	n/a
14	CCNT2	chr7:135931929-135932232	K562	blood:	n/a	n/a
15	CCNT2	chr7:135930053-135930542	K562	blood:	n/a	n/a
16	CEBPB	chr7:135929931-135930434	K562	blood:	n/a	n/a
17	CEBPB	chr7:135932979-135933054	K562	blood:	n/a	chr7:135932998-135933011 chr7:135932998-135933011
18	CEBPB	chr7:135902717-135902907	K562	blood:	n/a	chr7:135902816-135902825 chr7:135902814-135902825
19	CEBPB	chr7:135929999-135930429	K562	blood:	n/a	n/a
20	CEBPB	chr7:135887017-135887359	K562	blood:	n/a	n/a
21	CEBPB	chr7:135933754-135933876	K562	blood:	n/a	n/a
22	CEBPD	chr7:135929921-135930579	K562	blood:	n/a	n/a
23	CEBPD	chr7:135929988-135930518	K562	blood:	n/a	n/a
24	CTCF	chr7:135899240-135899390	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr7:135899260-135899410	BE2_C	brain:	n/a	n/a
26	CTCF	chr7:135899520-135899670	K562	blood:	n/a	n/a
27	CTCF	chr7:135899280-135899430	K562	blood:	n/a	n/a
28	CTCF	chr7:135899240-135899390	GM12872	blood:	n/a	n/a
29	CTCF	chr7:135899240-135899390	HRE	kidney:	n/a	n/a
30	CTCF	chr7:135899260-135899410	AG04450	lung:	n/a	n/a
31	CTCF	chr7:135899220-135899370	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr7:135899160-135899310	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr7:135899320-135899470	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr7:135899100-135899250	HCT-116	colon:	n/a	n/a
35	CTCF	chr7:135899180-135899330	HA-sp	spinal cord:	n/a	n/a
36	CTCF	chr7:135899160-135899310	AG04450	lung:	n/a	n/a
37	CTCF	chr7:135899275-135899359	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr7:135899240-135899390	BE2_C	brain:	n/a	n/a
39	CTCF	chr7:135899200-135899350	GM12864	blood:	n/a	n/a
40	CTCF	chr7:135899220-135899370	MCF-7	breast:	n/a	n/a
41	CTCF	chr7:135899200-135899350	GM12878	blood:	n/a	n/a
42	CTCF	chr7:135899220-135899370	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr7:135908995-135909050	GM13976	blood:	n/a	n/a
44	CTCF	chr7:135899260-135899410	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr7:135932180-135932330	GM06990	blood:	n/a	n/a
46	CTCF	chr7:135899240-135899390	RPTEC	kidney:	n/a	n/a
47	CTCF	chr7:135899192-135899386	IMR90	lung:	n/a	n/a
48	CTCF	chr7:135913370-135913413	Lung_OC	lung:	n/a	n/a
49	CTCF	chr7:135920090-135920161	Lung_OC	lung:	n/a	n/a
50	CTCF	chr7:135899260-135899410	HRPEpiC	eye:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:135938950-135939000	AG09309	skin:	n/a
2	chr7:135938950-135939000	HRE	kidney:	n/a
3	chr7:135938950-135939000	Jurkat	blood:	n/a
4	chr7:135938950-135939000	NB4	blood:	n/a
5	chr7:135938950-135939000	Hela-S3	cervix:	n/a
6	chr7:135938950-135939000	GM19239	blood:	n/a
7	chr7:135938950-135939000	HUVEC	blood vessel:	n/a
8	chr7:135938950-135939000	AoSMC	blood vessel:	n/a
9	chr7:135938950-135939000	HCT-116	colon:	n/a
10	chr7:135938950-135939000	Caco-2	colon:	n/a
11	chr7:135938950-135939000	GM12892	blood:	n/a
12	chr7:135938950-135939000	IMR90	lung:	fetal
13	chr7:135938950-135939000	HEEpiC	esophagus:	n/a
14	chr7:135938950-135939000	HRPEpiC	eye:	n/a
15	chr7:135938950-135939000	AG04449	skin:	fetal
16	chr7:135938950-135939000	NHDF-neo	bronchial:	n/a
17	chr7:135938950-135939000	A549	lung:	n/a
18	chr7:135938950-135939000	PANC-1	pancreas:	n/a
19	chr7:135938950-135939000	HCM	heart:	n/a
20	chr7:135938950-135939000	HNPCEpiC	eye:	n/a
21	chr7:135938950-135939000	MCF10A-Er-Src	breast:	n/a
22	chr7:135938950-135939000	SKMC	muscle:	n/a
23	chr7:135938950-135939000	AG09319	gingival:	n/a
24	chr7:135938950-135939000	K562	blood:	n/a
25	chr7:135938950-135939000	H1-hESC	embryonic stem cell:	embryo
26	chr7:135938950-135939000	SK-N-MC	brain:	n/a
27	chr7:135938950-135939000	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:135938950-135939000	HL-60	blood:	n/a
29	chr7:135938950-135939000	BE2_C	brain:	n/a
30	chr7:135938950-135939000	RPTEC	kidney:	n/a
31	chr7:135938950-135939000	HIPEpiC	eye:	n/a
32	chr7:135938950-135939000	PFSK-1	brain:	n/a
33	chr7:135938950-135939000	SK-N-SH	brain:	n/a
34	chr7:135938950-135939000	SAEC	small airway:	n/a
35	chr7:135938950-135939000	AG10803	skin:	n/a
36	chr7:135938950-135939000	HCPEpiC	choroid plexus:	n/a
37	chr7:135938950-135939000	HEK293	kidney:	embryo
38	chr7:135938950-135939000	HepG2	liver:	n/a
39	chr7:135938950-135939000	HAEpiC	amniotic membrane:	n/a
40	chr7:135938950-135939000	ECC-1	luminal epithelium:	n/a
41	chr7:135938950-135939000	GM12891	blood:	n/a
42	chr7:135938950-135939000	GM12878	blood:	n/a
43	chr7:135938950-135939000	BJ	skin:	n/a
44	chr7:135938950-135939000	CMK	blood:	n/a
45	chr7:135938950-135939000	NT2-D1	testis:	n/a
46	chr7:135938950-135939000	Hepatocyte	liver:	n/a
47	chr7:135938950-135939000	NHBE	bronchial:	n/a
48	chr7:135938950-135939000	U87	brain:	n/a
49	chr7:135938950-135939000	HRCEpiC	kidney:	n/a
50	chr7:135938950-135939000	MCF-7	breast:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:135887570..135889713-chr7:135900025..135901819,2	K562	blood:
2	chr7:135890212..135893020-chr7:135896104..135898612,2	K562	blood:
3	chr7:135895003..135896635-chr7:135898642..135900508,2	K562	blood:
4	chr7:135348191..135350354-chr7:135915037..135917617,2	K562	blood:
5	chr7:135890212..135893020-chr7:135896104..135898612,2	K562	blood:
6	chr7:135913397..135914921-chr7:135917469..135919011,2	K562	blood:
7	chr7:135904376..135906256-chr7:135913327..135915875,2	K562	blood:
8	chr7:135923364..135924230-chr8:93753197..93753880,2	MCF-7	breast:
9	chr7:135914976..135916896-chr7:135930254..135932259,2	K562	blood:
10	chr7:135917405..135919301-chr7:135920842..135922833,2	K562	blood:
11	chr7:135894378..135896833-chr7:135914235..135916684,2	K562	blood:
12	chr7:135913397..135914921-chr7:135917469..135919011,2	K562	blood:
13	chr7:135925867..135928083-chr7:135931669..135933724,2	K562	blood:
14	chr7:135895003..135896635-chr7:135898642..135900508,2	K562	blood:
15	chr7:135925867..135928083-chr7:135931669..135933724,2	K562	blood:
16	chr7:135887570..135889713-chr7:135900025..135901819,2	K562	blood:
17	chr7:135863093..135864946-chr7:135889140..135890969,2	K562	blood:
18	chr7:135886736..135888941-chr7:135890238..135892774,2	K562	blood:
19	chr7:135917405..135919301-chr7:135920842..135922833,2	K562	blood:
20	chr7:135880894..135883113-chr7:135885005..135887434,2	K562	blood:
21	chr7:135886736..135888941-chr7:135890238..135892774,2	K562	blood:
22	chr7:135922145..135923762-chr7:135932917..135934651,2	K562	blood:
23	chr7:135894378..135896833-chr7:135914235..135916684,2	K562	blood:
24	chr7:135922145..135923762-chr7:135932917..135934651,2	K562	blood:
25	chr7:135896650..135898487-chr7:135926765..135928429,2	K562	blood:
26	chr7:135871453..135873315-chr7:135899511..135901972,2	K562	blood:
27	chr7:135896650..135898487-chr7:135926765..135928429,2	K562	blood:
28	chr7:135901171..135902875-chr7:135904714..135906876,2	K562	blood:
29	chr7:135914976..135916896-chr7:135930254..135932259,2	K562	blood:
30	chr7:135901171..135902875-chr7:135904714..135906876,2	K562	blood:
31	chr7:135904376..135906256-chr7:135913327..135915875,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC015987.1-5	chr7:135894272-135895171	NONHSAT123546
2	lnc-AC015987.1-6	chr7:135895203-135896013	NONHSAT123547
3	lnc-CHRM2-2	chr7:135926898-135927119	ENSG00000232053.2
4	lnc-CHRM2-2	chr7:135926898-135927106	ENSG00000232053

No data

Variant related genes	Relation type
ENSG00000220982	TF binding region
ENSG00000220982	CpG island

Extended variants
information (count: 1213 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1213 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557267758	chr7:135886237-135886238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186526346	chr7:135886265-135886266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569800567	chr7:135886301-135886302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10225343	chr7:135886320-135886321	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs575918580	chr7:135886346-135886347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs17243535	chr7:135886453-135886454	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs145483309	chr7:135886466-135886467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138034351	chr7:135886472-135886473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572284517	chr7:135886474-135886475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs17243556	chr7:135886489-135886490	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs554848964	chr7:135886502-135886503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573950713	chr7:135886565-135886566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539726486	chr7:135886628-135886629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190627586	chr7:135886701-135886702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576159948	chr7:135886731-135886732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183494900	chr7:135886770-135886771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs834813	chr7:135886783-135886784	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs527890333	chr7:135886835-135886836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188389814	chr7:135886842-135886843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145270576	chr7:135886926-135886927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191308670	chr7:135886951-135886952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561665268	chr7:135887028-135887029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183062709	chr7:135887037-135887038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549775127	chr7:135887233-135887234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569688745	chr7:135887299-135887300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538701724	chr7:135887378-135887379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372908542	chr7:135887467-135887468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374105003	chr7:135887471-135887472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552307306	chr7:135887476-135887477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs834814	chr7:135887515-135887516	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs534867701	chr7:135887540-135887541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377048782	chr7:135887637-135887638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141911227	chr7:135887668-135887669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574712841	chr7:135887710-135887711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553225781	chr7:135887782-135887783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536231774	chr7:135887803-135887804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187797509	chr7:135887820-135887821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576044790	chr7:135887856-135887857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs117260512	chr7:135887870-135887871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565042658	chr7:135887875-135887876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572296216	chr7:135887892-135887893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541644241	chr7:135887927-135887928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370177102	chr7:135887928-135887929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561399049	chr7:135887949-135887950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146301307	chr7:135888061-135888062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550220643	chr7:135888097-135888098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191386848	chr7:135888112-135888113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184685153	chr7:135888123-135888124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545118719	chr7:135888141-135888142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557993081	chr7:135888151-135888152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Neuroticism	17667963	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute myeloid leukemia	17237825	CNVD
Esophageal cancer	21851588	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:135886200-135897600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr7:135895800-135900800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr7:135897600-135898000	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
4	chr7:135902600-135903400	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr7:135907200-135907400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr7:135908000-135908200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr7:135913000-135913200	Enhancers	Duodenum Smooth Muscle	Duodenum
8	chr7:135913000-135913200	Flanking Bivalent TSS/Enh	Esophagus	oesophagus
9	chr7:135914000-135914600	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr7:135914400-135914800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr7:135914600-135915000	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr7:135914800-135917000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr7:135918600-135919600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:135919200-135919600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr7:135919600-135919800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr7:135920400-135921400	ZNF genes & repeats	K562	blood
17	chr7:135921400-135921800	Weak transcription	K562	blood
18	chr7:135921800-135922400	Enhancers	K562	blood
19	chr7:135922200-135923000	Enhancers	Fetal Heart	heart
20	chr7:135922400-135925800	Weak transcription	K562	blood
21	chr7:135925200-135925600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr7:135925800-135927200	Enhancers	K562	blood
23	chr7:135927200-135929600	Weak transcription	K562	blood
24	chr7:135929600-135930000	Enhancers	K562	blood
25	chr7:135930000-135930800	Flanking Active TSS	K562	blood
26	chr7:135930800-135933800	Enhancers	K562	blood
27	chr7:135933400-135933800	Enhancers	Placenta	Placenta

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