Variant report

Variant	esv3345948
Chromosome Location	chr4:2826204-2829002
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:105)
CpG islands
(count:368)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:105 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr4:2828373-2828446	GM12891	blood:	n/a	n/a
2	CTCF	chr4:2828042-2828189	GM19239	blood:	n/a	n/a
3	CTCF	chr4:2827819-2827863	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr4:2828268-2828344	GM12892	blood:	n/a	n/a
5	CTCF	chr4:2827888-2827894	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr4:2828025-2828033	GM19239	blood:	n/a	n/a
7	CTCF	chr4:2827218-2827228	GM12892	blood:	n/a	n/a
8	CTCF	chr4:2827199-2827291	GM19239	blood:	n/a	n/a
9	CTCF	chr4:2827092-2827249	GM12891	blood:	n/a	n/a
10	CTCF	chr4:2828192-2828466	GM19239	blood:	n/a	n/a
11	JUND	chr4:2827984-2828385	HepG2	liver:	n/a	n/a
12	MYC	chr4:2828393-2828404	MCF-7	breast:	n/a	n/a
13	MYC	chr4:2827205-2827242	MCF-7	breast:	n/a	n/a
14	MYC	chr4:2827978-2828246	MCF-7	breast:	n/a	n/a
15	MYC	chr4:2828279-2828403	HUVEC	blood vessel:	n/a	n/a
16	MYC	chr4:2827318-2827321	MCF-7	breast:	n/a	n/a
17	MYC	chr4:2827300-2827318	GM12878	blood:	n/a	n/a
18	MYC	chr4:2827152-2827177	MCF-7	breast:	n/a	n/a
19	MYC	chr4:2828250-2828264	MCF-7	breast:	n/a	n/a
20	MYC	chr4:2828054-2828459	GM12878	blood:	n/a	n/a
21	MYC	chr4:2828172-2828304	MCF-7	breast:	n/a	n/a
22	MYC	chr4:2828257-2828271	HUVEC	blood vessel:	n/a	n/a
23	MYC	chr4:2827267-2827295	MCF-7	breast:	n/a	n/a
24	MYC	chr4:2828800-2828808	HUVEC	blood vessel:	n/a	n/a
25	MYC	chr4:2828333-2828336	MCF-7	breast:	n/a	n/a
26	NR2C2	chr4:2827913-2828871	GM12878	blood:	n/a	n/a
27	POLR2A	chr4:2828440-2828445	MCF-7	breast:	n/a	n/a
28	POLR2A	chr4:2826550-2826807	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr4:2827811-2828590	GM12891	blood:	n/a	n/a
30	POLR2A	chr4:2827769-2828381	SK-N-MC	brain:	n/a	n/a
31	POLR2A	chr4:2828483-2828490	Gliobla	brain:	n/a	n/a
32	POLR2A	chr4:2827167-2828038	HL-60	blood:	n/a	n/a
33	POLR2A	chr4:2827002-2827497	GM12891	blood:	n/a	n/a
34	POLR2A	chr4:2828644-2828897	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr4:2827150-2827288	MCF-7	breast:	n/a	n/a
36	POLR2A	chr4:2828334-2828428	HUVEC	blood vessel:	n/a	n/a
37	POLR2A	chr4:2827710-2827796	GM12878	blood:	n/a	n/a
38	POLR2A	chr4:2827775-2828557	GM12878	blood:	n/a	n/a
39	POLR2A	chr4:2828880-2828921	GM12878	blood:	n/a	n/a
40	POLR2A	chr4:2828177-2828187	K562	blood:	n/a	n/a
41	POLR2A	chr4:2827759-2828544	GM12892	blood:	n/a	n/a
42	POLR2A	chr4:2827117-2827580	H1-neurons	neurons:	n/a	n/a
43	POLR2A	chr4:2828248-2828481	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr4:2826998-2827411	GM12892	blood:	n/a	n/a
45	POLR2A	chr4:2827891-2828154	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr4:2827978-2828244	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr4:2828024-2828381	MCF-7	breast:	n/a	n/a
48	POLR2A	chr4:2828714-2828726	GM12878	blood:	n/a	n/a
49	POLR2A	chr4:2827641-2829065	GM12878	blood:	n/a	n/a
50	POLR2A	chr4:2827128-2827372	H1-hESC	embryonic stem cell:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:2826347-2826397	HNPCEpiC	eye:	n/a
2	chr4:2828170-2828220	SK-N-SH_RA	brain:	n/a
3	chr4:2826347-2826397	HNPCEpiC	eye:	n/a
4	chr4:2828170-2828220	SK-N-SH_RA	brain:	n/a
5	chr4:2828170-2828220	Caco-2	colon:	n/a
6	chr4:2828170-2828220	HCPEpiC	choroid plexus:	n/a
7	chr4:2826347-2826397	HAEpiC	amniotic membrane:	n/a
8	chr4:2826347-2826397	NH-A	brain:	n/a
9	chr4:2827061-2827111	HAEpiC	amniotic membrane:	n/a
10	chr4:2827194-2827244	AG09309	skin:	n/a
11	chr4:2827126-2827176	SK-N-MC	brain:	n/a
12	chr4:2826347-2826397	Hela-S3	cervix:	n/a
13	chr4:2827194-2827244	HIPEpiC	eye:	n/a
14	chr4:2828170-2828220	NT2-D1	testis:	n/a
15	chr4:2827061-2827111	T-47D	breast:	n/a
16	chr4:2827126-2827176	GM12878	blood:	n/a
17	chr4:2826420-2826470	GM12891	blood:	n/a
18	chr4:2826347-2826397	T-47D	breast:	n/a
19	chr4:2826347-2826397	BE2_C	brain:	n/a
20	chr4:2827194-2827244	SK-N-SH_RA	brain:	n/a
21	chr4:2827061-2827111	NHBE	bronchial:	n/a
22	chr4:2826420-2826470	GM06990	blood:	n/a
23	chr4:2826420-2826470	HEEpiC	esophagus:	n/a
24	chr4:2826347-2826397	GM12878	blood:	n/a
25	chr4:2827126-2827176	K562	blood:	n/a
26	chr4:2826420-2826470	HPAEpiC	pulmonary alveolar:	n/a
27	chr4:2827061-2827111	HPAEpiC	pulmonary alveolar:	n/a
28	chr4:2826347-2826397	PFSK-1	brain:	n/a
29	chr4:2828170-2828220	PFSK-1	brain:	n/a
30	chr4:2826420-2826470	NHDF-neo	bronchial:	n/a
31	chr4:2827061-2827111	HEK293	kidney:	embryo
32	chr4:2826420-2826470	IMR90	lung:	fetal
33	chr4:2827194-2827244	HUVEC	blood vessel:	n/a
34	chr4:2826347-2826397	NHBE	bronchial:	n/a
35	chr4:2827194-2827244	SK-N-MC	brain:	n/a
36	chr4:2826347-2826397	HL-60	blood:	n/a
37	chr4:2827061-2827111	A549	lung:	n/a
38	chr4:2827194-2827244	PANC-1	pancreas:	n/a
39	chr4:2827126-2827176	Jurkat	blood:	n/a
40	chr4:2826420-2826470	HEK293	kidney:	embryo
41	chr4:2826420-2826470	AG09309	skin:	n/a
42	chr4:2826420-2826470	HRPEpiC	eye:	n/a
43	chr4:2827194-2827244	Hela-S3	cervix:	n/a
44	chr4:2827194-2827244	NH-A	brain:	n/a
45	chr4:2827126-2827176	GM12891	blood:	n/a
46	chr4:2826347-2826397	AG09309	skin:	n/a
47	chr4:2827061-2827111	PFSK-1	brain:	n/a
48	chr4:2827061-2827111	IMR90	lung:	fetal
49	chr4:2828170-2828220	K562	blood:	n/a
50	chr4:2828170-2828220	HRPEpiC	eye:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:2826806..2829298-chr4:2829987..2832015,2	MCF-7	breast:
2	chr4:2794178..2796870-chr4:2828744..2832985,4	MCF-7	breast:
3	chr4:2822103..2824509-chr4:2824545..2827389,5	MCF-7	breast:
4	chr4:2824960..2827685-chr4:2829062..2834190,6	MCF-7	breast:
5	chr4:2758015..2760240-chr4:2824118..2826427,2	MCF-7	breast:
6	chr4:2822347..2826976-chr4:2843259..2846653,5	MCF-7	breast:
7	chr4:2794820..2799191-chr4:2824314..2827597,4	MCF-7	breast:
8	chr4:2824402..2830718-chr4:2842859..2847645,11	MCF-7	breast:
9	chr4:2819835..2821345-chr4:2824048..2826876,2	MCF-7	breast:

No data

Variant related genes	Relation type
SH3BP2	TF binding region
SH3BP2	CpG island
ENSG00000087266	chromatin interactions
ENSG00000168884	chromatin interactions
ENSG00000087274	chromatin interactions

Extended variants
information (count: 217 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:217 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75140118	chr4:2826218-2826219	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs540582773	chr4:2826219-2826220	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs113446832	chr4:2826260-2826261	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs532385141	chr4:2826261-2826262	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs552065108	chr4:2826271-2826272	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs371031275	chr4:2826275-2826276	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs184385853	chr4:2826288-2826289	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs139626310	chr4:2826347-2826348	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs149515000	chr4:2826352-2826353	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs140326137	chr4:2826376-2826377	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs548574112	chr4:2826396-2826397	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs142051964	chr4:2826399-2826400	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs3213501	chr4:2826400-2826401	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs368951667	chr4:2826420-2826421	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs140178337	chr4:2826421-2826422	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs554077647	chr4:2826433-2826434	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs1135633	chr4:2826442-2826443	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs539664951	chr4:2826449-2826450	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs372711589	chr4:2826450-2826451	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs143851218	chr4:2826452-2826453	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs62620003	chr4:2826472-2826473	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs370698624	chr4:2826474-2826475	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs370858278	chr4:2826478-2826479	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs142099137	chr4:2826529-2826530	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs543923186	chr4:2826644-2826645	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs371761201	chr4:2826652-2826653	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs574528136	chr4:2826656-2826657	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs540220040	chr4:2826667-2826668	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs73794809	chr4:2826671-2826672	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs35463251	chr4:2826693-2826694	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs532421849	chr4:2826720-2826721	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs545995919	chr4:2826725-2826726	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs187236640	chr4:2826755-2826756	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs191685921	chr4:2826756-2826757	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs548433420	chr4:2826761-2826762	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs568199147	chr4:2826773-2826774	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs113241482	chr4:2826783-2826784	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs114645897	chr4:2826807-2826808	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs56103814	chr4:2826815-2826816	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs371211628	chr4:2826823-2826824	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs376306035	chr4:2826824-2826825	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs199799999	chr4:2826840-2826841	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs367702206	chr4:2826872-2826873	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs371805150	chr4:2826885-2826886	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs539701566	chr4:2826911-2826912	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs16843413	chr4:2826912-2826913	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs113416255	chr4:2826932-2826933	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs369642567	chr4:2826947-2826948	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs536041097	chr4:2826957-2826958	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs112439699	chr4:2826958-2826959	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	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
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Ependymoma	20639864	CNVD
Facial dysmorphism	22438245	CNVD
Wolf-Hirschhorn syndrome	22438245	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:205 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2815800-2827000	Weak transcription	Fetal Heart	heart
2	chr4:2820400-2827600	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr4:2820600-2827200	Weak transcription	Aorta	Aorta
4	chr4:2820600-2827200	Weak transcription	Brain Cingulate Gyrus	brain
5	chr4:2820600-2832400	Weak transcription	NHDF-Ad	bronchial
6	chr4:2820600-2839000	Weak transcription	Right Atrium	heart
7	chr4:2820600-2839200	Weak transcription	Brain Angular Gyrus	brain
8	chr4:2820600-2844600	Weak transcription	Psoas Muscle	Psoas
9	chr4:2820800-2827000	Weak transcription	Fetal Kidney	kidney
10	chr4:2820800-2828200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:2820800-2835200	Weak transcription	HUVEC	blood vessel
12	chr4:2820800-2835400	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr4:2820800-2839600	Weak transcription	NHEK	skin
14	chr4:2821000-2844400	Weak transcription	HMEC	breast
15	chr4:2821200-2831400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr4:2821200-2834200	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr4:2821200-2835400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr4:2821400-2828600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr4:2821400-2836200	Strong transcription	Primary neutrophils fromperipheralblood	blood
20	chr4:2821400-2837800	Weak transcription	Small Intestine	intestine
21	chr4:2821600-2827000	Weak transcription	GM12878-XiMat	blood
22	chr4:2821600-2827400	Strong transcription	Fetal Stomach	stomach
23	chr4:2821600-2835400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
24	chr4:2821800-2828600	Weak transcription	Primary hematopoietic stem cells	blood
25	chr4:2821800-2828600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr4:2821800-2835800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr4:2821800-2835800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr4:2821800-2838000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr4:2821800-2838000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr4:2821800-2838200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr4:2821800-2838600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr4:2821800-2838800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr4:2821800-2844200	Weak transcription	Hela-S3	cervix
34	chr4:2822000-2826800	Strong transcription	Fetal Muscle Leg	muscle
35	chr4:2822000-2827200	Strong transcription	Primary T helper cells PMA-I stimulated	--
36	chr4:2822000-2831600	Weak transcription	NH-A	brain
37	chr4:2822000-2833600	Strong transcription	Primary B cells from cord blood	blood
38	chr4:2822000-2835200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr4:2822000-2835600	Strong transcription	Colonic Mucosa	Colon
40	chr4:2822000-2836000	Strong transcription	Primary T cells from cord blood	blood
41	chr4:2822000-2837200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:2822000-2837600	Strong transcription	HUES6 Cell Line	embryonic stem cell
43	chr4:2822200-2836400	Strong transcription	Thymus	Thymus
44	chr4:2822200-2837600	Strong transcription	Rectal Mucosa Donor 29	rectum
45	chr4:2822400-2827000	Weak transcription	Fetal Brain Male	brain
46	chr4:2822400-2828200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr4:2822400-2835800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr4:2822400-2838200	Strong transcription	Cortex derived primary cultured neurospheres	brain
49	chr4:2822600-2827000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr4:2822600-2827600	Strong transcription	Ovary	ovary

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