Variant report

Variant	esv3436317
Chromosome Location	chr4:1208602-1211100
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:189)
CpG islands
(count:489)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:189 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:1208963-1209677	GM12878	blood:	n/a	n/a
2	BCL11A	chr4:1209157-1209563	GM12878	blood:	n/a	n/a
3	BCLAF1	chr4:1208969-1209695	GM12878	blood:	n/a	chr4:1209624-1209633
4	BHLHE40	chr4:1209295-1209629	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:1210702-1211061	GM12878	blood:	n/a	n/a
6	CEBPB	chr4:1209279-1209582	GM12878	blood:	n/a	n/a
7	CEBPB	chr4:1209147-1209683	GM12878	blood:	n/a	n/a
8	CHD1	chr4:1209884-1210032	GM12878	blood:	n/a	n/a
9	CHD2	chr4:1209215-1209552	GM12878	blood:	n/a	n/a
10	CTCF	chr4:1210660-1210810	GM12865	blood:	n/a	n/a
11	CTCF	chr4:1210800-1210950	GM12875	blood:	n/a	n/a
12	CTCF	chr4:1210680-1210830	GM12873	blood:	n/a	n/a
13	CTCF	chr4:1210780-1210930	GM12868	blood:	n/a	n/a
14	CTCF	chr4:1210740-1210890	GM12873	blood:	n/a	n/a
15	CTCF	chr4:1210560-1210830	GM12869	blood:	n/a	n/a
16	CTCF	chr4:1210780-1210930	GM12872	blood:	n/a	n/a
17	CTCF	chr4:1210620-1210870	GM12801	blood:	n/a	n/a
18	CTCF	chr4:1210635-1210656	GM10248	blood:	n/a	n/a
19	CTCF	chr4:1208980-1209130	HPF	lung:	n/a	n/a
20	CTCF	chr4:1210720-1210870	GM12867	blood:	n/a	n/a
21	CTCF	chr4:1208940-1209090	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr4:1210760-1210910	GM12875	blood:	n/a	n/a
23	CTCF	chr4:1209249-1209364	GM12891	blood:	n/a	n/a
24	CTCF	chr4:1210700-1210850	GM12864	blood:	n/a	n/a
25	CTCF	chr4:1210680-1210830	AG04450	lung:	n/a	n/a
26	CTCF	chr4:1210720-1210870	GM12874	blood:	n/a	n/a
27	CTCF	chr4:1209020-1209170	GM12865	blood:	n/a	n/a
28	CTCF	chr4:1210760-1210910	GM12873	blood:	n/a	n/a
29	CTCF	chr4:1209000-1209150	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr4:1209205-1209374	GM12892	blood:	n/a	chr4:1209223-1209236
31	CTCF	chr4:1210187-1210189	GM19239	blood:	n/a	n/a
32	CTCF	chr4:1210740-1210890	GM12871	blood:	n/a	n/a
33	CTCF	chr4:1208640-1208790	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr4:1210740-1210890	GM12866	blood:	n/a	n/a
35	CTCF	chr4:1210790-1210833	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr4:1210680-1210830	GM12864	blood:	n/a	n/a
37	CTCF	chr4:1210780-1210930	GM12874	blood:	n/a	n/a
38	CTCF	chr4:1210740-1210890	GM12865	blood:	n/a	n/a
39	CTCF	chr4:1210660-1210810	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr4:1210620-1210770	GM12869	blood:	n/a	n/a
41	CTCF	chr4:1210723-1210895	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr4:1210196-1210250	GM19239	blood:	n/a	n/a
43	CTCF	chr4:1209386-1209466	GM12891	blood:	n/a	n/a
44	CTCF	chr4:1208980-1209130	GM12867	blood:	n/a	n/a
45	CTCF	chr4:1210720-1210870	GM06990	blood:	n/a	n/a
46	CTCF	chr4:1210780-1210930	GM12866	blood:	n/a	n/a
47	CTCF	chr4:1210660-1210810	HPF	lung:	n/a	n/a
48	CTCF	chr4:1210720-1210870	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr4:1208880-1209030	HMF	breast:	n/a	n/a
50	CTCF	chr4:1208720-1208870	HBMEC	blood vessel:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1208675-1208725	HRE	kidney:	n/a
2	chr4:1208675-1208725	HRE	kidney:	n/a
3	chr4:1208960-1209010	Jurkat	blood:	n/a
4	chr4:1208737-1208787	GM12891	blood:	n/a
5	chr4:1208699-1208749	HCT-116	colon:	n/a
6	chr4:1210478-1210528	PANC-1	pancreas:	n/a
7	chr4:1208699-1208749	AoSMC	blood vessel:	n/a
8	chr4:1208699-1208749	HNPCEpiC	eye:	n/a
9	chr4:1208699-1208749	PFSK-1	brain:	n/a
10	chr4:1208960-1209010	AG09309	skin:	n/a
11	chr4:1208737-1208787	RPTEC	kidney:	n/a
12	chr4:1210066-1210116	NH-A	brain:	n/a
13	chr4:1210066-1210116	NB4	blood:	n/a
14	chr4:1208737-1208787	SKMC	muscle:	n/a
15	chr4:1210066-1210116	HPAEpiC	pulmonary alveolar:	n/a
16	chr4:1208699-1208749	AG04449	skin:	fetal
17	chr4:1210478-1210528	HCT-116	colon:	n/a
18	chr4:1209971-1210021	GM06990	blood:	n/a
19	chr4:1210066-1210116	A549	lung:	n/a
20	chr4:1208960-1209010	Caco-2	colon:	n/a
21	chr4:1210478-1210528	HIPEpiC	eye:	n/a
22	chr4:1208960-1209010	HNPCEpiC	eye:	n/a
23	chr4:1208699-1208749	T-47D	breast:	n/a
24	chr4:1208699-1208749	NH-A	brain:	n/a
25	chr4:1210478-1210528	BJ	skin:	n/a
26	chr4:1208960-1209010	GM12878	blood:	n/a
27	chr4:1209971-1210021	HRE	kidney:	n/a
28	chr4:1209971-1210021	HEEpiC	esophagus:	n/a
29	chr4:1208960-1209010	HepG2	liver:	n/a
30	chr4:1208699-1208749	A549	lung:	n/a
31	chr4:1210066-1210116	BE2_C	brain:	n/a
32	chr4:1209844-1209894	GM06990	blood:	n/a
33	chr4:1208960-1209010	PFSK-1	brain:	n/a
34	chr4:1210478-1210528	HCPEpiC	choroid plexus:	n/a
35	chr4:1209844-1209894	AG09309	skin:	n/a
36	chr4:1209971-1210021	HRPEpiC	eye:	n/a
37	chr4:1210066-1210116	HUVEC	blood vessel:	n/a
38	chr4:1208737-1208787	NH-A	brain:	n/a
39	chr4:1208675-1208725	AG09319	gingival:	n/a
40	chr4:1210478-1210528	HMEC	breast:	n/a
41	chr4:1209971-1210021	NH-A	brain:	n/a
42	chr4:1208699-1208749	NB4	blood:	n/a
43	chr4:1208737-1208787	GM06990	blood:	n/a
44	chr4:1208699-1208749	Hela-S3	cervix:	n/a
45	chr4:1208699-1208749	CMK	blood:	n/a
46	chr4:1209844-1209894	T-47D	breast:	n/a
47	chr4:1209971-1210021	SKMC	muscle:	n/a
48	chr4:1208737-1208787	SK-N-SH	brain:	n/a
49	chr4:1208675-1208725	U87	brain:	n/a
50	chr4:1208699-1208749	PANC-1	pancreas:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:1205834..1208746-chr4:1226457..1228401,2	K562	blood:
2	chr4:1207031..1209938-chr4:1240960..1243998,4	K562	blood:
3	chr4:1209494..1211546-chr4:1218177..1220594,3	MCF-7	breast:
4	chr4:1203383..1207466-chr4:1208474..1210757,3	K562	blood:
5	chr4:1199021..1202194-chr4:1205945..1209496,3	K562	blood:
6	chr4:1210297..1212921-chr4:1219688..1223007,3	K562	blood:
7	chr2:86422601..86423306-chr4:1209197..1209717,2	MCF-7	breast:
8	chr4:1208349..1210341-chr4:1211100..1213340,2	MCF-7	breast:
9	chr4:1210359..1211936-chr4:1235947..1237642,2	K562	blood:
10	chr2:86422281..86424225-chr4:1209194..1210696,2	K562	blood:
11	chr4:1207031..1209440-chr4:1241875..1243998,2	K562	blood:
12	chr4:1160724..1161481-chr4:1208619..1209214,2	K562	blood:

No data

Variant related genes	Relation type
CTBP1	TF binding region
CTBP1	CpG island
ENSG00000273080	chromatin interactions
ENSG00000159692	chromatin interactions
ENSG00000159674	chromatin interactions
ENSG00000196810	chromatin interactions
ENSG00000132305	chromatin interactions

Extended variants
information (count: 133 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:133 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541529810	chr4:1208604-1208605	Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs559742661	chr4:1208610-1208611	Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs533367027	chr4:1208629-1208630	Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs114616313	chr4:1208643-1208644	Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs111334471	chr4:1208645-1208646	Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs3775109	chr4:1208703-1208704	Strong transcription Genic enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs530714090	chr4:1208726-1208727	Strong transcription Genic enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs184577673	chr4:1208738-1208739	Strong transcription Genic enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs548931074	chr4:1208768-1208769	Strong transcription Genic enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs567472423	chr4:1208769-1208770	Strong transcription Genic enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs112060964	chr4:1208784-1208785	Strong transcription Genic enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs6840663	chr4:1208806-1208807	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs375502652	chr4:1208812-1208813	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs538287997	chr4:1208843-1208844	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs558013600	chr4:1208846-1208847	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs189847868	chr4:1208855-1208856	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs140735918	chr4:1208866-1208867	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs555645932	chr4:1208911-1208912	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs540824571	chr4:1208917-1208918	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs192202713	chr4:1208975-1208976	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs184524519	chr4:1209026-1209027	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs553548891	chr4:1209046-1209047	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs578060500	chr4:1209073-1209074	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs535208989	chr4:1209111-1209112	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs563550681	chr4:1209129-1209130	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs138452063	chr4:1209158-1209159	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs1265923	chr4:1209174-1209175	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs560876424	chr4:1209213-1209214	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs529578439	chr4:1209228-1209229	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs528337327	chr4:1209230-1209231	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs143293917	chr4:1209272-1209273	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs571044094	chr4:1209289-1209290	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs189416949	chr4:1209310-1209311	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs113781022	chr4:1209368-1209369	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs550133500	chr4:1209373-1209374	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs3755951	chr4:1209383-1209384	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs537304306	chr4:1209440-1209441	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs556027914	chr4:1209446-1209447	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs567755130	chr4:1209447-1209448	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs535259278	chr4:1209481-1209482	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs111337493	chr4:1209489-1209490	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs578162440	chr4:1209498-1209499	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs545538023	chr4:1209502-1209503	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs563220557	chr4:1209521-1209522	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs557353420	chr4:1209528-1209529	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs547234468	chr4:1209552-1209553	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs182017336	chr4:1209592-1209593	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs542556923	chr4:1209639-1209640	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs561278483	chr4:1209650-1209651	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs141426450	chr4:1209663-1209664	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Breast cancer	17142309	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	20932292	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20393555	CNVD

Chromatin state (count:269 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1195200-1214600	Weak transcription	A549	lung
2	chr4:1196400-1209800	Weak transcription	Primary B cells from cord blood	blood
3	chr4:1198000-1211200	Genic enhancers	Fetal Stomach	stomach
4	chr4:1201600-1211600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:1201800-1209000	Strong transcription	Fetal Thymus	thymus
6	chr4:1201800-1210000	Strong transcription	Thymus	Thymus
7	chr4:1202200-1209000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:1202400-1210000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr4:1202600-1210200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr4:1202800-1210200	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr4:1202800-1218000	Weak transcription	Fetal Brain Male	brain
12	chr4:1203000-1209600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr4:1203000-1210200	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr4:1203200-1217800	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr4:1203400-1209200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr4:1203400-1210200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:1203400-1213000	Weak transcription	Fetal Kidney	kidney
18	chr4:1203800-1223000	Strong transcription	Osteobl	bone
19	chr4:1204000-1209400	Strong transcription	Primary T helper cells PMA-I stimulated	--
20	chr4:1204000-1211600	Genic enhancers	Esophagus	oesophagus
21	chr4:1204000-1218000	Weak transcription	K562	blood
22	chr4:1204200-1209200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr4:1204200-1209200	Strong transcription	Dnd41	blood
24	chr4:1204200-1212600	Genic enhancers	Fetal Muscle Leg	muscle
25	chr4:1204400-1209200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr4:1204400-1210000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr4:1204400-1210400	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr4:1204400-1210800	Strong transcription	Fetal Intestine Large	intestine
29	chr4:1204400-1211600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
30	chr4:1204400-1211600	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr4:1204400-1211600	Genic enhancers	Fetal Muscle Trunk	muscle
32	chr4:1204400-1212000	Strong transcription	NHEK	skin
33	chr4:1204400-1227200	Strong transcription	Fetal Intestine Small	intestine
34	chr4:1204400-1235800	Strong transcription	HUES6 Cell Line	embryonic stem cell
35	chr4:1204600-1209000	Strong transcription	Primary T helper cells fromperipheralblood	blood
36	chr4:1204600-1209000	Weak transcription	NH-A	brain
37	chr4:1204600-1210000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr4:1204600-1210200	Weak transcription	Fetal Heart	heart
39	chr4:1204600-1220400	Strong transcription	Liver	Liver
40	chr4:1204600-1236200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr4:1204800-1211000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr4:1204800-1212000	Strong transcription	H1 Cell Line	embryonic stem cell
43	chr4:1204800-1213800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr4:1204800-1226400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:1204800-1237000	Weak transcription	Psoas Muscle	Psoas
46	chr4:1205000-1208800	Strong transcription	Rectal Mucosa Donor 29	rectum
47	chr4:1205000-1210000	Strong transcription	Sigmoid Colon	Sigmoid Colon
48	chr4:1205000-1210200	Strong transcription	HUES48 Cell Line	embryonic stem cell
49	chr4:1205000-1210600	Weak transcription	Small Intestine	intestine
50	chr4:1205000-1211000	Weak transcription	Right Atrium	heart

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