Variant report

Variant	nsv1001832
Chromosome Location	chr4:9811805-9897520
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:428)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:9850013-9850273	K562	blood:	n/a	n/a
2	ATF2	chr4:9814641-9815054	GM12878	blood:	n/a	n/a
3	ATF3	chr4:9849946-9850297	K562	blood:	n/a	n/a
4	BACH1	chr4:9885168-9885286	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr4:9814682-9815071	GM12878	blood:	n/a	n/a
6	BATF	chr4:9813621-9813815	GM12878	blood:	n/a	n/a
7	BATF	chr4:9814742-9814999	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:9814677-9815008	GM12878	blood:	n/a	n/a
9	BCL11A	chr4:9814557-9814998	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:9851148-9851550	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:9851100-9851523	GM12878	blood:	n/a	n/a
12	BCL3	chr4:9826836-9827129	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:9867363-9867483	K562	blood:	n/a	n/a
14	BHLHE40	chr4:9872224-9872359	K562	blood:	n/a	n/a
15	BHLHE40	chr4:9851061-9851588	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:9814583-9815072	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:9882590-9882646	K562	blood:	n/a	n/a
18	BRCA1	chr4:9829608-9829617	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr4:9871086-9871272	GM12878	blood:	n/a	n/a
20	CCNT2	chr4:9895028-9895704	K562	blood:	n/a	n/a
21	CEBPB	chr4:9876209-9876280	K562	blood:	n/a	chr4:9876241-9876252
22	CEBPB	chr4:9849994-9850220	MCF-7	breast:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
23	CEBPB	chr4:9888675-9888963	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:9849998-9850279	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
25	CEBPB	chr4:9849980-9850299	H1-hESC	embryonic stem cell:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
26	CEBPB	chr4:9849869-9850308	HCT-116	colon:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
27	CEBPB	chr4:9849993-9850301	A549	lung:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
28	CEBPB	chr4:9895305-9895547	K562	blood:	n/a	n/a
29	CEBPB	chr4:9867161-9867312	HepG2	liver:	n/a	chr4:9867238-9867249
30	CEBPB	chr4:9876089-9876404	IMR90	lung:	n/a	chr4:9876241-9876252
31	CEBPB	chr4:9849824-9850326	HCT-116	colon:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
32	CEBPB	chr4:9849900-9850296	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
33	CEBPB	chr4:9849949-9850302	HepG2	liver:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
34	CEBPB	chr4:9895337-9895676	K562	blood:	n/a	n/a
35	CEBPB	chr4:9876127-9876348	HepG2	liver:	n/a	chr4:9876241-9876252
36	CEBPB	chr4:9849913-9850318	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
37	CEBPB	chr4:9849953-9850289	Hela-S3	cervix:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
38	CEBPB	chr4:9849942-9850300	IMR90	lung:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
39	CEBPD	chr4:9895295-9895750	K562	blood:	n/a	chr4:9895425-9895436
40	CEBPD	chr4:9895204-9895804	K562	blood:	n/a	chr4:9895425-9895436
41	CHD2	chr4:9851191-9851526	GM12878	blood:	n/a	n/a
42	CHD2	chr4:9850691-9850877	GM12878	blood:	n/a	n/a
43	CTCF	chr4:9878980-9879130	HCT-116	colon:	n/a	n/a
44	CTCF	chr4:9871470-9871497	GM20000	blood:	n/a	n/a
45	CTCF	chr4:9869580-9869730	WERI-Rb-1	eye:	n/a	chr4:9869654-9869663
46	CTCF	chr4:9848690-9848729	LNCaP	prostate:	n/a	n/a
47	CTCF	chr4:9878853-9879069	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr4:9878890-9879022	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:9882460-9882610	HCPEpiC	choroid plexus:	n/a	chr4:9882529-9882537
50	CTCF	chr4:9847920-9848070	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9892887-9892937	PrEC	prostate:	n/a
2	chr4:9884128-9884178	HAEpiC	amniotic membrane:	n/a
3	chr4:9892887-9892937	MCF10A-Er-Src	breast:	n/a
4	chr4:9884128-9884178	SKMC	muscle:	n/a
5	chr4:9884128-9884178	BE2_C	brain:	n/a
6	chr4:9892887-9892937	AG04449	skin:	fetal
7	chr4:9884128-9884178	HRPEpiC	eye:	n/a
8	chr4:9884128-9884178	HepG2	liver:	n/a
9	chr4:9884128-9884178	HIPEpiC	eye:	n/a
10	chr4:9892887-9892937	NB4	blood:	n/a
11	chr4:9892887-9892937	HCM	heart:	n/a
12	chr4:9892887-9892937	ECC-1	luminal epithelium:	n/a
13	chr4:9884128-9884178	T-47D	breast:	n/a
14	chr4:9892887-9892937	GM12891	blood:	n/a
15	chr4:9884128-9884178	AoSMC	blood vessel:	n/a
16	chr4:9884128-9884178	ovcar-3	ovarian:	n/a
17	chr4:9892887-9892937	NHDF-neo	bronchial:	n/a
18	chr4:9892887-9892937	NH-A	brain:	n/a
19	chr4:9892887-9892937	HEK293	kidney:	embryo
20	chr4:9892887-9892937	HCPEpiC	choroid plexus:	n/a
21	chr4:9892887-9892937	BE2_C	brain:	n/a
22	chr4:9884128-9884178	PANC-1	pancreas:	n/a
23	chr4:9892887-9892937	PANC-1	pancreas:	n/a
24	chr4:9892887-9892937	SK-N-SH	brain:	n/a
25	chr4:9892887-9892937	HMEC	breast:	n/a
26	chr4:9892887-9892937	U87	brain:	n/a
27	chr4:9892887-9892937	IMR90	lung:	fetal
28	chr4:9884128-9884178	HCPEpiC	choroid plexus:	n/a
29	chr4:9892887-9892937	AG04450	lung:	fetal
30	chr4:9884128-9884178	SK-N-MC	brain:	n/a
31	chr4:9884128-9884178	BJ	skin:	n/a
32	chr4:9892887-9892937	GM12878	blood:	n/a
33	chr4:9892887-9892937	BJ	skin:	n/a
34	chr4:9884128-9884178	GM12892	blood:	n/a
35	chr4:9884128-9884178	NT2-D1	testis:	n/a
36	chr4:9884128-9884178	AG10803	skin:	n/a
37	chr4:9884128-9884178	SAEC	small airway:	n/a
38	chr4:9884128-9884178	Hela-S3	cervix:	n/a
39	chr4:9892887-9892937	ProgFib	skin:	n/a
40	chr4:9884128-9884178	NB4	blood:	n/a
41	chr4:9892887-9892937	HCT-116	colon:	n/a
42	chr4:9884128-9884178	AG04450	lung:	fetal
43	chr4:9884128-9884178	Hepatocyte	liver:	n/a
44	chr4:9892887-9892937	Jurkat	blood:	n/a
45	chr4:9884128-9884178	IMR90	lung:	fetal
46	chr4:9892887-9892937	Hepatocyte	liver:	n/a
47	chr4:9892887-9892937	HIPEpiC	eye:	n/a
48	chr4:9892887-9892937	H1-hESC	embryonic stem cell:	embryo
49	chr4:9892887-9892937	HUVEC	blood vessel:	n/a
50	chr4:9884128-9884178	HUVEC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:9869830..9872812-chr4:9880250..9882960,2	K562	blood:
2	chr4:9869830..9872812-chr4:9880250..9882960,2	K562	blood:
3	chr4:9841356..9843538-chr4:9847251..9848935,2	K562	blood:
4	chr4:9865151..9867306-chr4:9868074..9870913,3	MCF-7	breast:
5	chr4:9841356..9843538-chr4:9847251..9848935,2	K562	blood:
6	chr4:9865151..9867306-chr4:9868074..9870913,3	MCF-7	breast:
7	chr4:9827283..9829135-chr4:9829200..9831465,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DRD5-13	chr4:9814207-9814604	NONHSAT095145
2	lnc-WDR1-12	chr4:9870401-9871383	NONHSAT095146
3	lnc-WDR1-12	chr4:9873428-9874487	NONHSAT095146

No data

Variant related genes	Relation type
SLC2A9	TF binding region
SLC2A9	CpG island
ENSG00000109667	chromatin interactions

Extended variants
information (count: 3842 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:3842 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10005226	chr4:9811805-9811806	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150183610	chr4:9811829-9811830	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559246269	chr4:9811830-9811831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184033171	chr4:9811841-9811842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370001306	chr4:9811856-9811857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541652742	chr4:9811858-9811859	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529368235	chr4:9811859-9811860	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115809382	chr4:9811873-9811874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574605805	chr4:9811905-9811906	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187799332	chr4:9811925-9811926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190812657	chr4:9811975-9811976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530575576	chr4:9811997-9811998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549058363	chr4:9811999-9812000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545771797	chr4:9812065-9812066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116305437	chr4:9812078-9812079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182991141	chr4:9812084-9812085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546414679	chr4:9812122-9812123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565805058	chr4:9812133-9812134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145713786	chr4:9812175-9812176	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181872225	chr4:9812188-9812189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569945432	chr4:9812222-9812223	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537492096	chr4:9812278-9812279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558944804	chr4:9812345-9812346	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571125883	chr4:9812389-9812390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550128402	chr4:9812406-9812407	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187203131	chr4:9812418-9812419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192533880	chr4:9812424-9812425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs77392502	chr4:9812444-9812445	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535541675	chr4:9812489-9812490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs60642521	chr4:9812514-9812515	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs571437850	chr4:9812515-9812516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538868899	chr4:9812536-9812537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372675812	chr4:9812552-9812553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545789656	chr4:9812557-9812558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73804386	chr4:9812560-9812561	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs572820133	chr4:9812566-9812567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184564423	chr4:9812584-9812585	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540173716	chr4:9812613-9812614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1356643	chr4:9812741-9812742	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs113663455	chr4:9812749-9812750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs60759193	chr4:9812754-9812755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565823332	chr4:9812773-9812774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs115490582	chr4:9812777-9812778	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529169982	chr4:9812790-9812791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187481561	chr4:9812796-9812797	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563810941	chr4:9812825-9812826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530764060	chr4:9812830-9812831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542266587	chr4:9812837-9812838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552561629	chr4:9812839-9812840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571124568	chr4:9812857-9812858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
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
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
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
early-passage human iPS cells	21368824	CNVD
Sinonasal adenocarcinoma	21360264	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	17142309	CNVD
Glioma	20126413	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Obesity	21131291	CNVD
Schizophrenia	23813976	CNVD
Hepatocellular carcinoma	22267523	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:454 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9794600-9812600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:9798800-9815000	Weak transcription	Lung	lung
3	chr4:9799200-9819600	Weak transcription	HMEC	breast
4	chr4:9806200-9821200	Weak transcription	Fetal Intestine Small	intestine
5	chr4:9807000-9819800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:9808200-9832000	Weak transcription	Duodenum Mucosa	Duodenum
7	chr4:9808600-9813400	Strong transcription	HepG2	liver
8	chr4:9808800-9813200	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr4:9808800-9834400	Weak transcription	NHEK	skin
10	chr4:9810000-9830600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr4:9811000-9827000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr4:9811600-9813000	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr4:9812600-9813600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:9813000-9813800	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr4:9813000-9814600	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr4:9813200-9813400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr4:9813200-9816000	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr4:9813400-9814200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr4:9813400-9826600	Weak transcription	HepG2	liver
20	chr4:9813600-9816000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:9813800-9814400	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr4:9814000-9815000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr4:9814200-9814600	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr4:9814200-9814800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr4:9814200-9815200	Enhancers	GM12878-XiMat	blood
26	chr4:9814400-9821200	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr4:9814600-9815000	Enhancers	Fetal Lung	lung
28	chr4:9814600-9815200	Enhancers	Brain Cingulate Gyrus	brain
29	chr4:9814600-9815200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
30	chr4:9814800-9817600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr4:9815000-9815200	Enhancers	Lung	lung
32	chr4:9816000-9816800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr4:9816000-9817400	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr4:9816800-9818800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:9817400-9822400	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr4:9818800-9820200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:9819400-9819800	ZNF genes & repeats	Pancreas	Pancrea
38	chr4:9819600-9820200	Strong transcription	HMEC	breast
39	chr4:9819800-9821400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:9819800-9821400	Weak transcription	Pancreas	Pancrea
41	chr4:9820200-9820400	Enhancers	Esophagus	oesophagus
42	chr4:9820200-9820600	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr4:9820200-9826400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:9820200-9842600	Weak transcription	HMEC	breast
45	chr4:9820400-9833400	Weak transcription	Esophagus	oesophagus
46	chr4:9821000-9832400	Weak transcription	Liver	Liver
47	chr4:9821200-9821600	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
48	chr4:9821200-9821600	ZNF genes & repeats	Fetal Intestine Small	intestine
49	chr4:9821400-9821600	ZNF genes & repeats	Pancreas	Pancrea
50	chr4:9821400-9826800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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