Variant report

Variant	esv3439419
Chromosome Location	chr4:187121758-187126356
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:392)
CpG islands
(count:244)
Chromatin interactive
region (count:11)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:392 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:187124713-187124813	K562	blood:	n/a	n/a
2	ARID3A	chr4:187123009-187123375	HepG2	liver:	n/a	n/a
3	ATF1	chr4:187125220-187125793	K562	blood:	n/a	n/a
4	ATF3	chr4:187123084-187123309	K562	blood:	n/a	n/a
5	BCL3	chr4:187123689-187124048	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:187123023-187123354	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:187124362-187124827	K562	blood:	n/a	n/a
8	BHLHE40	chr4:187125626-187125724	K562	blood:	n/a	n/a
9	BHLHE40	chr4:187123027-187123351	HepG2	liver:	n/a	n/a
10	BHLHE40	chr4:187123095-187123359	K562	blood:	n/a	n/a
11	CBX3	chr4:187124447-187124877	K562	blood:	n/a	n/a
12	CBX3	chr4:187125169-187125671	K562	blood:	n/a	n/a
13	CCNT2	chr4:187124521-187124882	K562	blood:	n/a	n/a
14	CEBPB	chr4:187125277-187125735	IMR90	lung:	n/a	n/a
15	CEBPB	chr4:187123006-187123320	MCF-7	breast:	n/a	chr4:187123065-187123076
16	CEBPB	chr4:187125299-187125736	K562	blood:	n/a	n/a
17	CEBPB	chr4:187122990-187123265	Hela-S3	cervix:	n/a	chr4:187123065-187123076
18	CEBPB	chr4:187122970-187123240	A549	lung:	n/a	chr4:187123065-187123076
19	CEBPB	chr4:187122940-187123206	HepG2	liver:	n/a	chr4:187123065-187123076
20	CREB1	chr4:187125094-187125886	K562	blood:	n/a	n/a
21	CREB1	chr4:187123098-187123277	A549	lung:	n/a	n/a
22	CREB1	chr4:187124927-187126111	K562	blood:	n/a	n/a
23	CTCF	chr4:187123100-187123250	GM06990	blood:	n/a	n/a
24	CTCF	chr4:187122990-187123383	T-47D	breast:	n/a	n/a
25	CTCF	chr4:187123120-187123270	GM12864	blood:	n/a	n/a
26	CTCF	chr4:187125399-187125623	Lung_OC	lung:	n/a	n/a
27	CTCF	chr4:187123060-187123210	HCT-116	colon:	n/a	n/a
28	CTCF	chr4:187124507-187124680	K562	blood:	n/a	n/a
29	CTCF	chr4:187123080-187123230	HCT-116	colon:	n/a	n/a
30	CTCF	chr4:187123050-187123336	MCF-7	breast:	n/a	n/a
31	CTCF	chr4:187123025-187123305	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr4:187123076-187123322	Fibrobl	skin:	n/a	n/a
33	CTCF	chr4:187123025-187123381	A549	lung:	n/a	n/a
34	CTCF	chr4:187123120-187123270	GM12801	blood:	n/a	n/a
35	CTCF	chr4:187123101-187123297	NHEK	skin:	n/a	n/a
36	CTCF	chr4:187122598-187123620	HCT-116	colon:	n/a	n/a
37	CTCF	chr4:187123060-187123307	HepG2	liver:	n/a	n/a
38	CTCF	chr4:187123100-187123250	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr4:187123100-187123250	GM12878	blood:	n/a	n/a
40	CTCF	chr4:187123065-187123338	GM19239	blood:	n/a	n/a
41	CTCF	chr4:187123069-187123304	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr4:187123140-187123290	HCM	heart:	n/a	n/a
43	CTCF	chr4:187123100-187123250	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr4:187123081-187123325	MCF-7	breast:	n/a	n/a
45	CTCF	chr4:187123100-187123250	Caco-2	colon:	n/a	n/a
46	CTCF	chr4:187125504-187125510	Fibrobl	skin:	n/a	n/a
47	CTCF	chr4:187123140-187123290	GM12878	blood:	n/a	n/a
48	CTCF	chr4:187123120-187123270	SAEC	small airway:	n/a	n/a
49	CTCF	chr4:187123100-187123250	GM12868	blood:	n/a	n/a
50	CTCF	chr4:187125910-187125939	Kidney_OC	kidney:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187126114-187126164	LNCaP	prostate:	n/a
2	chr4:187126114-187126164	T-47D	breast:	n/a
3	chr4:187126114-187126164	RPTEC	kidney:	n/a
4	chr4:187126073-187126123	HEEpiC	esophagus:	n/a
5	chr4:187126073-187126123	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:187126073-187126123	PFSK-1	brain:	n/a
7	chr4:187125413-187125463	MCF-7	breast:	n/a
8	chr4:187126139-187126189	HAEpiC	amniotic membrane:	n/a
9	chr4:187125413-187125463	HCT-116	colon:	n/a
10	chr4:187125413-187125463	MCF10A-Er-Src	breast:	n/a
11	chr4:187126114-187126164	SK-N-SH_RA	brain:	n/a
12	chr4:187125413-187125463	AG09309	skin:	n/a
13	chr4:187126114-187126164	HPAEpiC	pulmonary alveolar:	n/a
14	chr4:187126073-187126123	HEK293	kidney:	embryo
15	chr4:187126114-187126164	NHBE	bronchial:	n/a
16	chr4:187125413-187125463	K562	blood:	n/a
17	chr4:187125413-187125463	AG04450	lung:	fetal
18	chr4:187126139-187126189	H1-hESC	embryonic stem cell:	embryo
19	chr4:187126139-187126189	A549	lung:	n/a
20	chr4:187126139-187126189	BE2_C	brain:	n/a
21	chr4:187126139-187126189	HRE	kidney:	n/a
22	chr4:187126139-187126189	NHBE	bronchial:	n/a
23	chr4:187126139-187126189	NH-A	brain:	n/a
24	chr4:187126139-187126189	NB4	blood:	n/a
25	chr4:187126139-187126189	HEEpiC	esophagus:	n/a
26	chr4:187126114-187126164	PrEC	prostate:	n/a
27	chr4:187126114-187126164	HCF	heart:	n/a
28	chr4:187126114-187126164	AG04450	lung:	fetal
29	chr4:187125413-187125463	HNPCEpiC	eye:	n/a
30	chr4:187125413-187125463	HRE	kidney:	n/a
31	chr4:187125413-187125463	SK-N-SH	brain:	n/a
32	chr4:187125413-187125463	HCF	heart:	n/a
33	chr4:187126114-187126164	HMEC	breast:	n/a
34	chr4:187126139-187126189	Hela-S3	cervix:	n/a
35	chr4:187126073-187126123	CMK	blood:	n/a
36	chr4:187126073-187126123	AG09319	gingival:	n/a
37	chr4:187126114-187126164	IMR90	lung:	fetal
38	chr4:187125413-187125463	HL-60	blood:	n/a
39	chr4:187126114-187126164	SK-N-MC	brain:	n/a
40	chr4:187126139-187126189	Hepatocyte	liver:	n/a
41	chr4:187126114-187126164	HIPEpiC	eye:	n/a
42	chr4:187125413-187125463	PFSK-1	brain:	n/a
43	chr4:187126139-187126189	SK-N-SH_RA	brain:	n/a
44	chr4:187125413-187125463	HRPEpiC	eye:	n/a
45	chr4:187126139-187126189	LNCaP	prostate:	n/a
46	chr4:187126114-187126164	Hela-S3	cervix:	n/a
47	chr4:187126114-187126164	GM19239	blood:	n/a
48	chr4:187125413-187125463	PANC-1	pancreas:	n/a
49	chr4:187125413-187125463	Jurkat	blood:	n/a
50	chr4:187126139-187126189	HCM	heart:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:187117801..187120230-chr4:187120810..187122503,2	K562	blood:
2	chr4:187058298..187058901-chr4:187122712..187123588,2	MCF-7	breast:
3	chr4:187109253..187118277-chr4:187122555..187126883,14	K562	blood:
4	chr4:187112006..187113547-chr4:187122764..187123712,6	MCF-7	breast:
5	chr4:187118539..187120138-chr4:187121607..187123644,3	MCF-7	breast:
6	chr4:187125089..187127684-chr4:187129515..187131962,3	K562	blood:
7	chr4:187111353..187115983-chr4:187119045..187124895,10	MCF-7	breast:
8	chr4:187116069..187118838-chr4:187120195..187124189,4	MCF-7	breast:
9	chr4:187122087..187123852-chr4:187421026..187423788,3	K562	blood:
10	chr4:187121686..187123375-chr4:187456206..187458817,2	K562	blood:
11	chr4:186988972..186989928-chr4:187122701..187123491,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLKB1-1	chr4:187125266-187125400	NONHSAT099647
2	lnc-KLKB1-1	chr4:187125555-187125774	NONHSAT099646
3	lnc-KLKB1-1	chr4:187125555-187125762	NONHSAT099648
4	lnc-KLKB1-1	chr4:187125389-187125458	NONHSAT099648
5	lnc-KLKB1-1	chr4:187125593-187125738	NONHSAT099647
6	lnc-KLKB1-1	chr4:187125257-187125426	NONHSAT099646

No data

Variant related genes	Relation type
CYP4V2	TF binding region
KLKB1	TF binding region
CYP4V2	CpG island
KLKB1	CpG island
ENSG00000145476	chromatin interactions
ENSG00000164344	chromatin interactions
ENSG00000269302	chromatin interactions
ENSG00000212387	chromatin interactions
ENSG00000251165	chromatin interactions
DOK3	miRNA target sites
EIF3J	miRNA target sites

Extended variants
information (count: 255 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376575307	chr4:187121807-187121808	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs72646271	chr4:187121808-187121809	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs72646272	chr4:187121930-187121931	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs149701759	chr4:187121952-187121953	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs72646273	chr4:187121953-187121954	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs182268875	chr4:187121955-187121956	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs539636066	chr4:187121975-187121976	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs576845784	chr4:187121997-187121998	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs72646274	chr4:187122002-187122003	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs7687961	chr4:187122009-187122010	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs113813388	chr4:187122011-187122012	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs186878730	chr4:187122017-187122018	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs7687818	chr4:187122060-187122061	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs72646275	chr4:187122096-187122097	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs536330293	chr4:187122101-187122102	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs371789104	chr4:187122106-187122107	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs572922305	chr4:187122107-187122108	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs544965394	chr4:187122188-187122189	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs11730880	chr4:187122204-187122205	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs150741959	chr4:187122266-187122267	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs139914147	chr4:187122267-187122268	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs563324444	chr4:187122288-187122289	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs530014373	chr4:187122303-187122304	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs3817184	chr4:187122304-187122305	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs377390043	chr4:187122312-187122313	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs556930061	chr4:187122319-187122320	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs17855071	chr4:187122320-187122321	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs34745240	chr4:187122332-187122333	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs72646276	chr4:187122340-187122341	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs142136741	chr4:187122341-187122342	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs3736456	chr4:187122355-187122356	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs200103451	chr4:187122364-187122365	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs370303148	chr4:187122371-187122372	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs140344168	chr4:187122411-187122412	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs375077034	chr4:187122440-187122441	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs144129557	chr4:187122460-187122461	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs199476194	chr4:187122467-187122468	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs199476195	chr4:187122480-187122481	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs200916028	chr4:187122482-187122483	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs199476196	chr4:187122483-187122484	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs149818768	chr4:187122499-187122500	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs367670100	chr4:187122534-187122535	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs536417542	chr4:187122560-187122561	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs386683482	chr4:187122590-187122591	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs183572214	chr4:187122592-187122593	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs564337293	chr4:187122596-187122597	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs545655417	chr4:187122669-187122670	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs563971583	chr4:187122670-187122671	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs539073047	chr4:187122702-187122703	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs188552512	chr4:187122781-187122782	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
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
Acute lymphoblastic leukemia	20067559	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
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187113600-187123800	Weak transcription	Fetal Brain Male	brain
2	chr4:187113600-187125200	Weak transcription	Gastric	stomach
3	chr4:187113800-187123200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr4:187113800-187124000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:187113800-187125200	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr4:187113800-187125400	Weak transcription	Esophagus	oesophagus
7	chr4:187113800-187126000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr4:187113800-187130600	Weak transcription	Stomach Mucosa	stomach
9	chr4:187113800-187131400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:187113800-187132200	Weak transcription	Colonic Mucosa	Colon
11	chr4:187114000-187122800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr4:187114000-187123000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr4:187114000-187123200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr4:187114000-187124400	Weak transcription	Fetal Lung	lung
15	chr4:187114000-187125200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr4:187114000-187133200	Weak transcription	HSMM	muscle
17	chr4:187114200-187122800	Weak transcription	Primary B cells from peripheral blood	blood
18	chr4:187114200-187123200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr4:187114200-187123800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr4:187114200-187124200	Weak transcription	K562	blood
21	chr4:187114200-187125200	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr4:187114200-187125200	Weak transcription	NHDF-Ad	bronchial
23	chr4:187114200-187126000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr4:187114400-187123600	Weak transcription	Fetal Kidney	kidney
25	chr4:187114400-187125200	Weak transcription	Primary hematopoietic stem cells	blood
26	chr4:187114400-187125200	Weak transcription	Osteobl	bone
27	chr4:187114600-187125200	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr4:187114600-187125200	Weak transcription	Right Atrium	heart
29	chr4:187114800-187130000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr4:187115000-187125200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr4:187115000-187125200	Weak transcription	NHLF	lung
32	chr4:187115200-187123800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:187115200-187124400	Weak transcription	Spleen	Spleen
34	chr4:187115200-187125200	Weak transcription	Psoas Muscle	Psoas
35	chr4:187115200-187125600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr4:187115200-187133600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr4:187115400-187123600	Weak transcription	Pancreas	Pancrea
38	chr4:187115400-187125200	Weak transcription	Fetal Brain Female	brain
39	chr4:187115400-187125200	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr4:187115400-187125600	Weak transcription	Brain Substantia Nigra	brain
41	chr4:187115400-187130400	Weak transcription	Small Intestine	intestine
42	chr4:187116800-187123800	Weak transcription	Thymus	Thymus
43	chr4:187116800-187125200	Weak transcription	Brain Angular Gyrus	brain
44	chr4:187116800-187125200	Weak transcription	Right Ventricle	heart
45	chr4:187116800-187125400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr4:187117000-187123000	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr4:187117000-187124800	Weak transcription	Placenta	Placenta
48	chr4:187117200-187125200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr4:187117400-187125600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr4:187117600-187121800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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