Variant report

Variant	nsv879704
Chromosome Location	chr4:107095901-107212966
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1127)
CpG islands
(count:183)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1127 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:107187312-107187673	K562	blood:	n/a	n/a
2	ARID3A	chr4:107208155-107209087	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:107122568-107122875	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:107185332-107186301	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:107187285-107187995	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:107158658-107158673	K562	blood:	n/a	n/a
7	ARID3A	chr4:107181297-107181568	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:107178933-107180099	HepG2	liver:	n/a	chr4:107179805-107179821
9	ARID3A	chr4:107122500-107122908	K562	blood:	n/a	chr4:107122543-107122559 chr4:107122542-107122558
10	ATF1	chr4:107187389-107187589	K562	blood:	n/a	n/a
11	ATF2	chr4:107160021-107160295	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:107132367-107132419	K562	blood:	n/a	n/a
13	BACH1	chr4:107208566-107208766	K562	blood:	n/a	n/a
14	BCL3	chr4:107129042-107129310	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:107208489-107208936	HepG2	liver:	n/a	n/a
16	BHLHE40	chr4:107179340-107179781	HepG2	liver:	n/a	n/a
17	BRCA1	chr4:107159962-107160052	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:107194916-107195223	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:107179222-107179822	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:107208509-107208805	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr4:107208499-107208883	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:107210930-107211279	IMR90	lung:	n/a	chr4:107211106-107211117
23	CEBPB	chr4:107208555-107208771	K562	blood:	n/a	n/a
24	CEBPB	chr4:107123476-107123689	K562	blood:	n/a	chr4:107123585-107123596
25	CEBPB	chr4:107181531-107181600	K562	blood:	n/a	n/a
26	CEBPB	chr4:107208500-107208865	MCF-7	breast:	n/a	n/a
27	CEBPB	chr4:107171708-107171998	K562	blood:	n/a	chr4:107171819-107171830
28	CEBPB	chr4:107130249-107130501	A549	lung:	n/a	chr4:107130336-107130349
29	CEBPB	chr4:107208457-107208866	K562	blood:	n/a	n/a
30	CEBPB	chr4:107130236-107130498	HepG2	liver:	n/a	chr4:107130336-107130349
31	CEBPB	chr4:107208523-107208852	MCF-7	breast:	n/a	n/a
32	CEBPB	chr4:107181493-107181684	IMR90	lung:	n/a	n/a
33	CEBPB	chr4:107208530-107208859	A549	lung:	n/a	n/a
34	CEBPB	chr4:107208448-107208893	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:107195003-107195124	K562	blood:	n/a	n/a
36	CEBPB	chr4:107113405-107113567	K562	blood:	n/a	n/a
37	CEBPB	chr4:107208460-107208882	A549	lung:	n/a	n/a
38	CEBPB	chr4:107171749-107171973	HepG2	liver:	n/a	chr4:107171819-107171830
39	CEBPB	chr4:107208234-107209215	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:107096804-107097116	IMR90	lung:	n/a	chr4:107096936-107096947
41	CEBPB	chr4:107208355-107208987	A549	lung:	n/a	n/a
42	CEBPB	chr4:107123436-107123705	HepG2	liver:	n/a	chr4:107123585-107123596
43	CEBPB	chr4:107130226-107130488	Hela-S3	cervix:	n/a	chr4:107130336-107130349
44	CEBPB	chr4:107194992-107195201	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr4:107192497-107192652	HepG2	liver:	n/a	chr4:107192544-107192557 chr4:107192545-107192556
46	CEBPB	chr4:107210968-107211264	A549	lung:	n/a	chr4:107211106-107211117
47	CEBPB	chr4:107209111-107209146	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr4:107096846-107097088	HepG2	liver:	n/a	chr4:107096936-107096947
49	CEBPB	chr4:107210994-107211254	Hela-S3	cervix:	n/a	chr4:107211106-107211117
50	CEBPB	chr4:107212930-107213211	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:107177868-107177918	HIPEpiC	eye:	n/a
2	chr4:107130107-107130157	HCT-116	colon:	n/a
3	chr4:107208133-107208183	HL-60	blood:	n/a
4	chr4:107130107-107130157	SAEC	small airway:	n/a
5	chr4:107177868-107177918	AG09319	gingival:	n/a
6	chr4:107130107-107130157	Jurkat	blood:	n/a
7	chr4:107208133-107208183	K562	blood:	n/a
8	chr4:107177868-107177918	Hepatocyte	liver:	n/a
9	chr4:107177868-107177918	LNCaP	prostate:	n/a
10	chr4:107177868-107177918	ECC-1	luminal epithelium:	n/a
11	chr4:107208133-107208183	HEEpiC	esophagus:	n/a
12	chr4:107130107-107130157	HUVEC	blood vessel:	n/a
13	chr4:107208133-107208183	AoSMC	blood vessel:	n/a
14	chr4:107177868-107177918	HNPCEpiC	eye:	n/a
15	chr4:107177868-107177918	SAEC	small airway:	n/a
16	chr4:107130107-107130157	HRE	kidney:	n/a
17	chr4:107177868-107177918	HCPEpiC	choroid plexus:	n/a
18	chr4:107177868-107177918	GM12892	blood:	n/a
19	chr4:107208133-107208183	NT2-D1	testis:	n/a
20	chr4:107177868-107177918	T-47D	breast:	n/a
21	chr4:107208133-107208183	GM19239	blood:	n/a
22	chr4:107208133-107208183	HIPEpiC	eye:	n/a
23	chr4:107130107-107130157	GM06990	blood:	n/a
24	chr4:107208133-107208183	LNCaP	prostate:	n/a
25	chr4:107130107-107130157	ovcar-3	ovarian:	n/a
26	chr4:107208133-107208183	BE2_C	brain:	n/a
27	chr4:107130107-107130157	A549	lung:	n/a
28	chr4:107130107-107130157	U87	brain:	n/a
29	chr4:107177868-107177918	AG10803	skin:	n/a
30	chr4:107208133-107208183	T-47D	breast:	n/a
31	chr4:107130107-107130157	AG04450	lung:	fetal
32	chr4:107177868-107177918	GM12891	blood:	n/a
33	chr4:107177868-107177918	NHBE	bronchial:	n/a
34	chr4:107208133-107208183	SK-N-SH_RA	brain:	n/a
35	chr4:107208133-107208183	HAEpiC	amniotic membrane:	n/a
36	chr4:107130107-107130157	HRPEpiC	eye:	n/a
37	chr4:107130107-107130157	NT2-D1	testis:	n/a
38	chr4:107208133-107208183	GM06990	blood:	n/a
39	chr4:107177868-107177918	HRE	kidney:	n/a
40	chr4:107130107-107130157	NHBE	bronchial:	n/a
41	chr4:107177868-107177918	HRPEpiC	eye:	n/a
42	chr4:107177868-107177918	NB4	blood:	n/a
43	chr4:107208133-107208183	HRE	kidney:	n/a
44	chr4:107177868-107177918	PrEC	prostate:	n/a
45	chr4:107130107-107130157	HEEpiC	esophagus:	n/a
46	chr4:107130107-107130157	GM12878	blood:	n/a
47	chr4:107208133-107208183	GM12878	blood:	n/a
48	chr4:107130107-107130157	PANC-1	pancreas:	n/a
49	chr4:107177868-107177918	RPTEC	kidney:	n/a
50	chr4:107208133-107208183	BJ	skin:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:107160677..107162898-chr4:107235492..107237232,2	MCF-7	breast:
2	chr4:107186600..107189007-chr4:107189607..107191897,2	K562	blood:
3	chr4:107187206..107187713-chr4:107739937..107740444,2	MCF-7	breast:
4	chr4:107180191..107183024-chr4:107184999..107187172,2	MCF-7	breast:
5	chr4:107186942..107188312-chr4:107422810..107424188,6	MCF-7	breast:
6	chr4:107186600..107189007-chr4:107189607..107191897,2	K562	blood:
7	chr4:107186651..107188040-chr4:107422951..107423909,9	K562	blood:
8	chr4:107184193..107185780-chr4:107235786..107237913,2	K562	blood:
9	chr4:107187507..107189111-chr4:107189607..107191483,2	K562	blood:
10	chr4:107194465..107196300-chr4:107236860..107239279,2	MCF-7	breast:
11	chr4:107167830..107170345-chr4:107178069..107180274,2	K562	blood:
12	chr4:107116810..107118888-chr4:107121036..107122571,2	K562	blood:
13	chr4:107170979..107173933-chr4:107183092..107185530,2	K562	blood:
14	chr4:107144706..107146969-chr4:107150712..107153683,3	K562	blood:
15	chr4:107129508..107131492-chr4:107132634..107135593,2	MCF-7	breast:
16	chr4:107187038..107188038-chr4:107249952..107250600,3	MCF-7	breast:
17	chr4:107116810..107118888-chr4:107121036..107122571,2	K562	blood:
18	chr4:107164698..107166859-chr4:107230939..107233039,2	K562	blood:
19	chr4:107185773..107187284-chr4:107235963..107237575,2	MCF-7	breast:
20	chr4:107142111..107144318-chr4:107145536..107147639,2	K562	blood:
21	chr2:88990302..88991116-chr4:107159175..107159797,2	MCF-7	breast:
22	chr4:107189189..107191825-chr4:107236392..107239313,3	MCF-7	breast:
23	chr4:107183968..107186758-chr4:107242517..107245278,3	K562	blood:
24	chr4:107157087..107158697-chr4:107236510..107238674,2	MCF-7	breast:
25	chr4:107142111..107144318-chr4:107145536..107147639,2	K562	blood:
26	chr4:106875594..106876144-chr4:107122239..107122877,2	MCF-7	breast:
27	chr4:107180191..107183024-chr4:107184999..107187172,2	MCF-7	breast:
28	chr4:107129974..107132069-chr4:107132979..107135565,2	MCF-7	breast:
29	chr4:107187507..107189111-chr4:107189607..107191483,2	K562	blood:

No data

Variant related genes	Relation type
TBCK	TF binding region
TBCK	CpG island
ENSG00000164022	chromatin interactions
ENSG00000145348	chromatin interactions

Extended variants
information (count: 3944 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3944 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10022339	chr4:107095901-107095902	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs373471039	chr4:107095984-107095985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368639882	chr4:107095998-107095999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531562961	chr4:107096035-107096036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs542707962	chr4:107096088-107096089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs138965082	chr4:107096181-107096182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142978300	chr4:107096192-107096193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182830528	chr4:107096230-107096231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561478801	chr4:107096241-107096242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545355727	chr4:107096248-107096249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533544005	chr4:107096252-107096253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs59940336	chr4:107096254-107096255	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs570770781	chr4:107096267-107096268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539758482	chr4:107096273-107096274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76322341	chr4:107096289-107096290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs78537459	chr4:107096290-107096291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184921863	chr4:107096304-107096305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186599727	chr4:107096305-107096306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs77782722	chr4:107096311-107096312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79456874	chr4:107096345-107096346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542441217	chr4:107096356-107096357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192548792	chr4:107096376-107096377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12642227	chr4:107096404-107096405	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs541389435	chr4:107096441-107096442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs79909961	chr4:107096455-107096456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11097917	chr4:107096480-107096481	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs545757758	chr4:107096509-107096510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34198925	chr4:107096516-107096517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562836167	chr4:107096626-107096627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148512538	chr4:107096640-107096641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528461105	chr4:107096692-107096693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561402226	chr4:107096707-107096708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10000428	chr4:107096708-107096709	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs78005162	chr4:107096893-107096894	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs112716052	chr4:107096932-107096933	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs184771270	chr4:107096939-107096940	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs544672130	chr4:107096954-107096955	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs150642434	chr4:107097037-107097038	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs550188220	chr4:107097106-107097107	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs139882192	chr4:107097113-107097114	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs535667635	chr4:107097150-107097151	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs555998339	chr4:107097162-107097163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572530908	chr4:107097171-107097172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535145676	chr4:107097172-107097173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187589431	chr4:107097175-107097176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143833138	chr4:107097269-107097270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146871249	chr4:107097288-107097289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562639993	chr4:107097294-107097295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10025725	chr4:107097310-107097311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572256377	chr4:107097316-107097317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Cognitive impairment	21505072	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1698 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:107038000-107112000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr4:107053800-107101600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr4:107054000-107113600	Weak transcription	Brain Anterior Caudate	brain
4	chr4:107066400-107151200	Weak transcription	Colon Smooth Muscle	Colon
5	chr4:107071800-107176400	Weak transcription	Rectal Smooth Muscle	rectum
6	chr4:107074200-107114400	Weak transcription	NHDF-Ad	bronchial
7	chr4:107074600-107111800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr4:107075800-107114000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr4:107075800-107118200	Weak transcription	Brain Substantia Nigra	brain
10	chr4:107075800-107129600	Weak transcription	Spleen	Spleen
11	chr4:107076400-107114200	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr4:107078000-107107800	Weak transcription	HSMMtube	muscle
13	chr4:107078200-107116000	Weak transcription	Colonic Mucosa	Colon
14	chr4:107078800-107112200	Weak transcription	Osteobl	bone
15	chr4:107078800-107114200	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr4:107083200-107173400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr4:107083800-107114200	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr4:107083800-107134000	Weak transcription	Right Ventricle	heart
19	chr4:107083800-107164800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr4:107084000-107108600	Weak transcription	Duodenum Mucosa	Duodenum
21	chr4:107084000-107112200	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr4:107084000-107116400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr4:107084000-107129800	Weak transcription	Lung	lung
24	chr4:107084200-107096000	Weak transcription	Fetal Muscle Leg	muscle
25	chr4:107084200-107114000	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr4:107084200-107114000	Weak transcription	HepG2	liver
27	chr4:107084200-107114200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr4:107084200-107114200	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr4:107084200-107129600	Weak transcription	Aorta	Aorta
30	chr4:107084400-107112200	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr4:107084400-107141400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr4:107084600-107111600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr4:107085000-107114200	Weak transcription	Fetal Intestine Large	intestine
34	chr4:107085000-107114200	Weak transcription	Fetal Thymus	thymus
35	chr4:107085000-107117800	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr4:107085000-107129600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr4:107085000-107150000	Weak transcription	Dnd41	blood
38	chr4:107085400-107098800	Weak transcription	Primary T cells from cord blood	blood
39	chr4:107085400-107169600	Weak transcription	Fetal Kidney	kidney
40	chr4:107085600-107112200	Weak transcription	Primary B cells from peripheral blood	blood
41	chr4:107087000-107104400	Weak transcription	HSMM	muscle
42	chr4:107087200-107129800	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr4:107088400-107166400	Weak transcription	K562	blood
44	chr4:107088800-107116400	Weak transcription	NH-A	brain
45	chr4:107089600-107103600	Weak transcription	Placenta	Placenta
46	chr4:107091200-107114200	Weak transcription	Brain Hippocampus Middle	brain
47	chr4:107091200-107129200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr4:107091400-107098800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr4:107091400-107103600	Weak transcription	Primary hematopoietic stem cells	blood
50	chr4:107091400-107110600	Weak transcription	Primary T cells fromperipheralblood	blood

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