Variant report

Variant	esv1000327
Chromosome Location	chr4:10135604-10192545
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1641)
CpG islands
(count:551)
Chromatin interactive
region (count:134)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1641 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:10185222-10185607	K562	blood:	n/a	chr4:10185454-10185470
2	ARID3A	chr4:10174858-10175646	K562	blood:	n/a	n/a
3	ARID3A	chr4:10172580-10173201	K562	blood:	n/a	n/a
4	ARID3A	chr4:10188308-10188961	K562	blood:	n/a	n/a
5	ARID3A	chr4:10182036-10184108	K562	blood:	n/a	n/a
6	ARID3A	chr4:10175936-10176225	K562	blood:	n/a	n/a
7	ARID3A	chr4:10186847-10188023	K562	blood:	n/a	n/a
8	ARID3A	chr4:10159442-10159716	K562	blood:	n/a	n/a
9	ARID3A	chr4:10171356-10172376	K562	blood:	n/a	n/a
10	ATF1	chr4:10182216-10183403	K562	blood:	n/a	n/a
11	ATF1	chr4:10172681-10173016	K562	blood:	n/a	n/a
12	ATF1	chr4:10188186-10188661	K562	blood:	n/a	n/a
13	ATF1	chr4:10184693-10185042	K562	blood:	n/a	n/a
14	ATF1	chr4:10171263-10171804	K562	blood:	n/a	n/a
15	ATF1	chr4:10174911-10175439	K562	blood:	n/a	n/a
16	ATF1	chr4:10159418-10159720	K562	blood:	n/a	n/a
17	ATF1	chr4:10187244-10187892	K562	blood:	n/a	n/a
18	ATF2	chr4:10159321-10159751	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr4:10152775-10153075	GM12878	blood:	n/a	n/a
20	ATF2	chr4:10159305-10159743	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr4:10187352-10187768	K562	blood:	n/a	n/a
22	ATF3	chr4:10174879-10175394	K562	blood:	n/a	n/a
23	ATF3	chr4:10182376-10183375	K562	blood:	n/a	n/a
24	ATF3	chr4:10159392-10159666	K562	blood:	n/a	chr4:10159502-10159515
25	BACH1	chr4:10166957-10167185	K562	blood:	n/a	n/a
26	BACH1	chr4:10166286-10166294	K562	blood:	n/a	n/a
27	BACH1	chr4:10174959-10175395	K562	blood:	n/a	n/a
28	BACH1	chr4:10159277-10159771	K562	blood:	n/a	n/a
29	BACH1	chr4:10182278-10183266	K562	blood:	n/a	n/a
30	BACH1	chr4:10174334-10174335	K562	blood:	n/a	n/a
31	BACH1	chr4:10187292-10187596	K562	blood:	n/a	n/a
32	BACH1	chr4:10185169-10185293	K562	blood:	n/a	n/a
33	BATF	chr4:10182721-10182989	GM12878	blood:	n/a	n/a
34	BCL3	chr4:10182602-10183425	K562	blood:	n/a	chr4:10182894-10182903
35	BCL3	chr4:10191805-10192054	GM12878	blood:	n/a	n/a
36	BCLAF1	chr4:10182260-10183432	K562	blood:	n/a	chr4:10182894-10182903
37	BHLHE40	chr4:10175935-10175937	K562	blood:	n/a	n/a
38	BHLHE40	chr4:10174617-10175572	K562	blood:	n/a	n/a
39	BHLHE40	chr4:10181734-10182063	K562	blood:	n/a	n/a
40	BHLHE40	chr4:10189767-10190685	K562	blood:	n/a	n/a
41	BHLHE40	chr4:10173956-10174337	K562	blood:	n/a	n/a
42	BHLHE40	chr4:10159371-10160168	HepG2	liver:	n/a	chr4:10159971-10159980 chr4:10159965-10159986 chr4:10159971-10159980
43	BHLHE40	chr4:10142964-10143314	K562	blood:	n/a	n/a
44	BHLHE40	chr4:10159446-10159651	GM12878	blood:	n/a	n/a
45	BHLHE40	chr4:10163933-10164279	HepG2	liver:	n/a	n/a
46	BHLHE40	chr4:10177050-10177337	K562	blood:	n/a	n/a
47	BHLHE40	chr4:10187295-10189374	K562	blood:	n/a	n/a
48	BHLHE40	chr4:10186281-10186687	K562	blood:	n/a	n/a
49	BHLHE40	chr4:10164926-10165017	HepG2	liver:	n/a	n/a
50	BHLHE40	chr4:10159283-10159719	K562	blood:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10147606-10147656	T-47D	breast:	n/a
2	chr4:10145483-10145533	GM19239	blood:	n/a
3	chr4:10147606-10147656	T-47D	breast:	n/a
4	chr4:10145483-10145533	GM19239	blood:	n/a
5	chr4:10147100-10147150	ovcar-3	ovarian:	n/a
6	chr4:10147100-10147150	AG09309	skin:	n/a
7	chr4:10147302-10147352	SKMC	muscle:	n/a
8	chr4:10145483-10145533	LNCaP	prostate:	n/a
9	chr4:10145483-10145533	AG09309	skin:	n/a
10	chr4:10147038-10147088	AG10803	skin:	n/a
11	chr4:10147330-10147380	BJ	skin:	n/a
12	chr4:10147606-10147656	NHBE	bronchial:	n/a
13	chr4:10160060-10160110	K562	blood:	n/a
14	chr4:10160060-10160110	SK-N-SH	brain:	n/a
15	chr4:10149849-10149899	HPAEpiC	pulmonary alveolar:	n/a
16	chr4:10147100-10147150	IMR90	lung:	fetal
17	chr4:10147606-10147656	HCF	heart:	n/a
18	chr4:10145483-10145533	HMEC	breast:	n/a
19	chr4:10147606-10147656	HAEpiC	amniotic membrane:	n/a
20	chr4:10147330-10147380	Hela-S3	cervix:	n/a
21	chr4:10149849-10149899	CMK	blood:	n/a
22	chr4:10145483-10145533	HepG2	liver:	n/a
23	chr4:10143053-10143103	HCT-116	colon:	n/a
24	chr4:10143053-10143103	GM06990	blood:	n/a
25	chr4:10160060-10160110	HRCEpiC	kidney:	n/a
26	chr4:10143053-10143103	ECC-1	luminal epithelium:	n/a
27	chr4:10143053-10143103	Jurkat	blood:	n/a
28	chr4:10160060-10160110	AG10803	skin:	n/a
29	chr4:10147100-10147150	Jurkat	blood:	n/a
30	chr4:10160060-10160110	SK-N-SH_RA	brain:	n/a
31	chr4:10147302-10147352	T-47D	breast:	n/a
32	chr4:10147302-10147352	HRPEpiC	eye:	n/a
33	chr4:10160060-10160110	LNCaP	prostate:	n/a
34	chr4:10147100-10147150	HPAEpiC	pulmonary alveolar:	n/a
35	chr4:10143053-10143103	BE2_C	brain:	n/a
36	chr4:10147100-10147150	Hepatocyte	liver:	n/a
37	chr4:10160060-10160110	AoSMC	blood vessel:	n/a
38	chr4:10149849-10149899	SK-N-SH	brain:	n/a
39	chr4:10147330-10147380	SKMC	muscle:	n/a
40	chr4:10160060-10160110	NHDF-neo	bronchial:	n/a
41	chr4:10147302-10147352	GM06990	blood:	n/a
42	chr4:10145483-10145533	K562	blood:	n/a
43	chr4:10147330-10147380	SK-N-MC	brain:	n/a
44	chr4:10147038-10147088	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:10147302-10147352	CMK	blood:	n/a
46	chr4:10149849-10149899	AG10803	skin:	n/a
47	chr4:10149849-10149899	SAEC	small airway:	n/a
48	chr4:10160060-10160110	ovcar-3	ovarian:	n/a
49	chr4:10147606-10147656	AG04450	lung:	fetal
50	chr4:10147606-10147656	PFSK-1	brain:	n/a

(count:134 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:10166648..10168321-chr4:10402902..10405737,2	K562	blood:
2	chr4:10161449..10162536-chr4:10550736..10551916,8	MCF-7	breast:
3	chr4:10159101..10160040-chr4:10527876..10528788,2	K562	blood:
4	chr4:10180113..10182537-chr4:10415151..10418343,3	K562	blood:
5	chr4:10181386..10184366-chr4:10364568..10366943,2	K562	blood:
6	chr4:10166113..10167122-chr4:10405126..10405888,4	K562	blood:
7	chr4:10182491..10184302-chr4:10237283..10239761,2	K562	blood:
8	chr4:10166196..10167366-chr4:10404929..10406035,4	MCF-7	breast:
9	chr4:10160529..10162216-chr4:10164137..10166713,2	K562	blood:
10	chr4:10114162..10115900-chr4:10186432..10189186,2	K562	blood:
11	chr4:10182154..10184410-chr4:10456824..10459646,5	K562	blood:
12	chr4:10173514..10177541-chr4:10443857..10446930,3	K562	blood:
13	chr4:10159584..10164126-chr4:10173679..10176923,6	K562	blood:
14	chr4:10159186..10164011-chr4:10164137..10169302,8	K562	blood:
15	chr4:10138009..10140287-chr4:10142395..10145088,2	MCF-7	breast:
16	chr4:10184632..10187184-chr4:10400763..10402949,2	K562	blood:
17	chr4:10159186..10164011-chr4:10164137..10169302,8	K562	blood:
18	chr4:10118040..10120090-chr4:10149414..10151081,2	K562	blood:
19	chr4:10159444..10160410-chr4:10539265..10539788,2	K562	blood:
20	chr4:10143164..10147494-chr4:10150670..10153852,4	K562	blood:
21	chr4:10147623..10149514-chr4:10156130..10157999,2	K562	blood:
22	chr4:10150688..10152239-chr4:10154005..10156791,2	K562	blood:
23	chr4:10180991..10184001-chr4:10327240..10329402,3	K562	blood:
24	chr4:10156172..10158401-chr4:10178392..10179954,2	K562	blood:
25	chr4:10124769..10127534-chr4:10135159..10136966,2	MCF-7	breast:
26	chr4:10117542..10119864-chr4:10151862..10154716,2	MCF-7	breast:
27	chr4:10117300..10124855-chr4:10138380..10145377,13	MCF-7	breast:
28	chr4:10160663..10163901-chr4:10177399..10182680,5	K562	blood:
29	chr4:10151902..10153544-chr4:10159740..10162552,2	K562	blood:
30	chr4:10180991..10182787-chr4:10327240..10329402,2	K562	blood:
31	chr4:10181426..10184302-chr4:10237283..10239761,3	K562	blood:
32	chr4:10137029..10138548-chr4:10444331..10446997,2	K562	blood:
33	chr4:10183994..10188822-chr4:10326557..10329780,4	K562	blood:
34	chr4:10166490..10167101-chr4:10539409..10540077,2	MCF-7	breast:
35	chr4:10174527..10176209-chr4:10240126..10241692,2	K562	blood:
36	chr4:10116325..10123199-chr4:10169149..10177855,21	K562	blood:
37	chr4:10141623..10144820-chr4:10145857..10148531,3	K562	blood:
38	chr4:10166357..10167092-chr4:10539527..10540141,2	K562	blood:
39	chr4:10166411..10167001-chr4:10551169..10551934,2	MCF-7	breast:
40	chr4:10186571..10188279-chr4:10316070..10319056,2	K562	blood:
41	chr4:10187220..10189194-chr4:10403510..10406450,3	K562	blood:
42	chr4:10181799..10184639-chr4:10262185..10264664,2	K562	blood:
43	chr4:10146309..10149123-chr4:10156130..10158993,2	K562	blood:
44	chr4:10185102..10187379-chr4:10256972..10258730,2	K562	blood:
45	chr4:10155458..10156959-chr4:10169942..10172746,2	K562	blood:
46	chr4:10140841..10143166-chr4:10164924..10167000,2	K562	blood:
47	chr4:10118185..10123341-chr4:10157230..10162785,8	K562	blood:
48	chr4:10132922..10135214-chr4:10181103..10182859,2	K562	blood:
49	chr4:10160529..10162216-chr4:10164137..10166713,2	K562	blood:
50	chr4:10181502..10184182-chr4:38665329..38667544,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR1-4	chr4:10151989-10152058	NONHSAT095472
2	lnc-WDR1-4	chr4:10159007-10159491	NONHSAT095472
3	lnc-WDR1-2	chr4:10144991-10145279	NONHSAT095429
4	lnc-WDR1-6	chr4:10168783-10169389	NONHSAT095487

No data

Variant related genes	Relation type
ENSG00000251296	TF binding region
ENSG00000250393	TF binding region
ENSG00000251296	CpG island
ENSG00000250393	CpG island
ENSG00000251296	chromatin interactions
ENSG00000196355	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000231160	chromatin interactions
ENSG00000250393	chromatin interactions
ENSG00000178163	chromatin interactions
ENSG00000250040	chromatin interactions
ENSG00000109787	chromatin interactions
ENSG00000223086	chromatin interactions

Extended variants
information (count: 4551 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:4551 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546532515	chr4:10136804-10136805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs4358401	chr4:10136807-10136808	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs534075866	chr4:10136809-10136810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs192815279	chr4:10136831-10136832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555738499	chr4:10136834-10136835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200497290	chr4:10136842-10136843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs201678649	chr4:10136843-10136844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535241108	chr4:10136857-10136858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs544230548	chr4:10136874-10136875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184378068	chr4:10136876-10136877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189330687	chr4:10136883-10136884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs376714982	chr4:10136893-10136894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs58198247	chr4:10136895-10136896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs397941722	chr4:10136897-10136898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138501326	chr4:10136903-10136904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558951628	chr4:10136911-10136912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556593178	chr4:10136933-10136934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs115885584	chr4:10136960-10136961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535346697	chr4:10136964-10136965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189419756	chr4:10136978-10136979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs193124692	chr4:10136981-10136982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184806940	chr4:10136983-10136984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs575455464	chr4:10136987-10136988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs56201573	chr4:10137018-10137019	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs76547354	chr4:10137029-10137030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529995742	chr4:10137032-10137033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545872462	chr4:10137034-10137035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs564109921	chr4:10137040-10137041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189271355	chr4:10137041-10137042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181679869	chr4:10137043-10137044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546891436	chr4:10137047-10137048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556261124	chr4:10137050-10137051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529130275	chr4:10137062-10137063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs550409124	chr4:10137090-10137091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs138645884	chr4:10137093-10137094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185859750	chr4:10137096-10137097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs873984	chr4:10137125-10137126	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs71603990	chr4:10137129-10137130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552359526	chr4:10137133-10137134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189583960	chr4:10137161-10137162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564700457	chr4:10137181-10137182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534742095	chr4:10137185-10137186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10008628	chr4:10137201-10137202	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs552747993	chr4:10137202-10137203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs118181336	chr4:10137229-10137230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs181125921	chr4:10137232-10137233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142740833	chr4:10137245-10137246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186039170	chr4:10137273-10137274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146071624	chr4:10137294-10137295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191139076	chr4:10137295-10137296	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
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
Wilms tumour	21544195	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
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:629 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10136800-10137400	Enhancers	NHEK	skin
2	chr4:10136800-10137800	Enhancers	Fetal Heart	heart
3	chr4:10142400-10142800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr4:10142600-10142800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr4:10142600-10143000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:10142600-10143200	Enhancers	Fetal Thymus	thymus
7	chr4:10142800-10143000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr4:10142800-10143200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr4:10142800-10143200	Enhancers	H1 Cell Line	embryonic stem cell
10	chr4:10142800-10143200	Enhancers	H9 Cell Line	embryonic stem cell
11	chr4:10142800-10143200	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr4:10142800-10143200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
13	chr4:10142800-10151800	Weak transcription	Spleen	Spleen
14	chr4:10143000-10143200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr4:10143000-10143200	Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr4:10143000-10143200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr4:10143000-10143200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:10143200-10143600	Enhancers	Rectal Mucosa Donor 29	rectum
19	chr4:10143200-10149800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:10146200-10147000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:10146400-10146800	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr4:10146400-10147000	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr4:10146400-10147000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr4:10146400-10147600	Enhancers	Primary B cells from peripheral blood	blood
25	chr4:10146600-10147200	Bivalent Enhancer	Primary B cells from cord blood	blood
26	chr4:10149800-10150000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:10151000-10151200	Enhancers	Fetal Stomach	stomach
28	chr4:10151200-10164400	Weak transcription	Right Atrium	heart
29	chr4:10151400-10152400	Weak transcription	Fetal Stomach	stomach
30	chr4:10151800-10152000	Enhancers	Spleen	Spleen
31	chr4:10151800-10153000	Enhancers	Fetal Muscle Leg	muscle
32	chr4:10152000-10152200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
33	chr4:10152000-10153600	Enhancers	Primary B cells from cord blood	blood
34	chr4:10152200-10153800	Enhancers	Primary B cells from peripheral blood	blood
35	chr4:10152400-10152800	Enhancers	Fetal Stomach	stomach
36	chr4:10152600-10152800	Flanking Active TSS	GM12878-XiMat	blood
37	chr4:10152800-10153400	Enhancers	GM12878-XiMat	blood
38	chr4:10156800-10157000	Bivalent Enhancer	HSMMtube	muscle
39	chr4:10157600-10157800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
40	chr4:10157600-10160800	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr4:10158000-10160800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr4:10158600-10160000	Enhancers	Thymus	Thymus
43	chr4:10158600-10165600	Enhancers	Fetal Thymus	thymus
44	chr4:10158800-10159800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr4:10158800-10161000	Enhancers	Fetal Stomach	stomach
46	chr4:10158800-10161200	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr4:10159000-10160200	Enhancers	Brain Angular Gyrus	brain
48	chr4:10159000-10160800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr4:10159000-10160800	Enhancers	Brain Hippocampus Middle	brain
50	chr4:10159000-10160800	Enhancers	Brain Substantia Nigra	brain

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