Variant report

Variant	nsv880260
Chromosome Location	chr4:151214038-151331191
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1136)
CpG islands
(count:244)
Chromatin interactive
region (count:69)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1136 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:151219026-151219395	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:151242284-151242530	K562	blood:	n/a	n/a
3	ARID3A	chr4:151248771-151248939	K562	blood:	n/a	n/a
4	ARID3A	chr4:151269190-151269615	K562	blood:	n/a	n/a
5	ARID3A	chr4:151219015-151219398	K562	blood:	n/a	n/a
6	ARID3A	chr4:151278107-151278518	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:151250540-151250872	K562	blood:	n/a	n/a
8	ARID3A	chr4:151237450-151238409	K562	blood:	n/a	n/a
9	ARID3A	chr4:151239726-151240519	K562	blood:	n/a	n/a
10	ARID3A	chr4:151223718-151224036	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:151223647-151224071	K562	blood:	n/a	n/a
12	ARID3A	chr4:151236479-151236795	K562	blood:	n/a	n/a
13	ARID3A	chr4:151276500-151277743	HepG2	liver:	n/a	n/a
14	ATF1	chr4:151269269-151269551	K562	blood:	n/a	n/a
15	ATF1	chr4:151237449-151237783	K562	blood:	n/a	n/a
16	ATF1	chr4:151239797-151240565	K562	blood:	n/a	n/a
17	ATF1	chr4:151223671-151224016	K562	blood:	n/a	n/a
18	ATF2	chr4:151287811-151288219	GM12878	blood:	n/a	n/a
19	ATF2	chr4:151288427-151288847	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr4:151247032-151247422	GM12878	blood:	n/a	n/a
21	ATF2	chr4:151246941-151247453	GM12878	blood:	n/a	n/a
22	ATF3	chr4:151223759-151223954	HepG2	liver:	n/a	n/a
23	ATF3	chr4:151223717-151224098	HCT-116	colon:	n/a	n/a
24	ATF3	chr4:151240069-151240599	K562	blood:	n/a	n/a
25	ATF3	chr4:151223640-151224087	K562	blood:	n/a	n/a
26	ATF3	chr4:151223743-151223947	K562	blood:	n/a	n/a
27	ATF3	chr4:151223664-151224086	HCT-116	colon:	n/a	n/a
28	BACH1	chr4:151239786-151240008	K562	blood:	n/a	n/a
29	BACH1	chr4:151240223-151240381	K562	blood:	n/a	n/a
30	BATF	chr4:151287899-151288217	GM12878	blood:	n/a	n/a
31	BATF	chr4:151287832-151288212	GM12878	blood:	n/a	chr4:151287894-151287903
32	BCL11A	chr4:151288446-151288783	H1-hESC	embryonic stem cell:	n/a	n/a
33	BCL11A	chr4:151287634-151288172	GM12878	blood:	n/a	chr4:151288093-151288102
34	BCL11A	chr4:151288512-151288775	H1-hESC	embryonic stem cell:	n/a	n/a
35	BCL11A	chr4:151287787-151288222	GM12878	blood:	n/a	chr4:151288093-151288102
36	BHLHE40	chr4:151239763-151240538	K562	blood:	n/a	n/a
37	BHLHE40	chr4:151223650-151224051	K562	blood:	n/a	n/a
38	BHLHE40	chr4:151290979-151291234	K562	blood:	n/a	n/a
39	BHLHE40	chr4:151302936-151303132	GM12878	blood:	n/a	n/a
40	BHLHE40	chr4:151287842-151288128	GM12878	blood:	n/a	n/a
41	BHLHE40	chr4:151223704-151224033	HepG2	liver:	n/a	n/a
42	BHLHE40	chr4:151324165-151324449	K562	blood:	n/a	n/a
43	BHLHE40	chr4:151281647-151281713	K562	blood:	n/a	n/a
44	BHLHE40	chr4:151264621-151264775	K562	blood:	n/a	n/a
45	BHLHE40	chr4:151237520-151237882	K562	blood:	n/a	n/a
46	BHLHE40	chr4:151242223-151242653	K562	blood:	n/a	n/a
47	BRCA1	chr4:151269320-151269570	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr4:151223650-151224085	HCT-116	colon:	n/a	n/a
49	CBX3	chr4:151223586-151224036	K562	blood:	n/a	n/a
50	CBX3	chr4:151242191-151242751	K562	blood:	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	chr4:151231429-151231479	Hepatocyte	liver:	n/a
2	chr4:151287731-151287781	GM12878	blood:	n/a
3	chr4:151231429-151231479	NHDF-neo	bronchial:	n/a
4	chr4:151231429-151231479	HCM	heart:	n/a
5	chr4:151287731-151287781	PrEC	prostate:	n/a
6	chr4:151260569-151260619	GM12892	blood:	n/a
7	chr4:151258915-151258965	HCT-116	colon:	n/a
8	chr4:151287731-151287781	SK-N-MC	brain:	n/a
9	chr4:151260569-151260619	NB4	blood:	n/a
10	chr4:151258915-151258965	HL-60	blood:	n/a
11	chr4:151258915-151258965	AG09319	gingival:	n/a
12	chr4:151231429-151231479	U87	brain:	n/a
13	chr4:151231429-151231479	HPAEpiC	pulmonary alveolar:	n/a
14	chr4:151260569-151260619	HCF	heart:	n/a
15	chr4:151258915-151258965	HUVEC	blood vessel:	n/a
16	chr4:151260569-151260619	HUVEC	blood vessel:	n/a
17	chr4:151287731-151287781	HMEC	breast:	n/a
18	chr4:151231429-151231479	GM12892	blood:	n/a
19	chr4:151287731-151287781	ovcar-3	ovarian:	n/a
20	chr4:151258915-151258965	Caco-2	colon:	n/a
21	chr4:151258915-151258965	BE2_C	brain:	n/a
22	chr4:151231429-151231479	SAEC	small airway:	n/a
23	chr4:151258915-151258965	HEEpiC	esophagus:	n/a
24	chr4:151287731-151287781	SAEC	small airway:	n/a
25	chr4:151287731-151287781	HepG2	liver:	n/a
26	chr4:151287731-151287781	K562	blood:	n/a
27	chr4:151258915-151258965	ovcar-3	ovarian:	n/a
28	chr4:151258915-151258965	HNPCEpiC	eye:	n/a
29	chr4:151258915-151258965	NB4	blood:	n/a
30	chr4:151260569-151260619	GM12878	blood:	n/a
31	chr4:151287731-151287781	MCF-7	breast:	n/a
32	chr4:151231429-151231479	SK-N-SH_RA	brain:	n/a
33	chr4:151287731-151287781	NH-A	brain:	n/a
34	chr4:151258915-151258965	NHDF-neo	bronchial:	n/a
35	chr4:151287731-151287781	AG09309	skin:	n/a
36	chr4:151231429-151231479	SK-N-SH	brain:	n/a
37	chr4:151258915-151258965	GM06990	blood:	n/a
38	chr4:151260569-151260619	PrEC	prostate:	n/a
39	chr4:151258915-151258965	U87	brain:	n/a
40	chr4:151260569-151260619	HMEC	breast:	n/a
41	chr4:151231429-151231479	HRPEpiC	eye:	n/a
42	chr4:151260569-151260619	ProgFib	skin:	n/a
43	chr4:151287731-151287781	PFSK-1	brain:	n/a
44	chr4:151258915-151258965	SK-N-SH_RA	brain:	n/a
45	chr4:151260569-151260619	SAEC	small airway:	n/a
46	chr4:151287731-151287781	HUVEC	blood vessel:	n/a
47	chr4:151260569-151260619	GM12891	blood:	n/a
48	chr4:151231429-151231479	NB4	blood:	n/a
49	chr4:151287731-151287781	HIPEpiC	eye:	n/a
50	chr4:151260569-151260619	Jurkat	blood:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:151226062..151228889-chr4:151229626..151232770,4	K562	blood:
2	chr4:151319888..151322699-chr4:151326262..151329136,2	K562	blood:
3	chr4:151257124..151260042-chr4:151261309..151264282,4	K562	blood:
4	chr4:151275871..151278702-chr4:151280509..151282712,2	K562	blood:
5	chr4:151249582..151252300-chr4:151272970..151274932,2	K562	blood:
6	chr4:151242129..151245111-chr4:151249733..151251799,3	K562	blood:
7	chr4:151314752..151316835-chr4:151320252..151322487,2	K562	blood:
8	chr4:150920189..150921053-chr4:151218927..151219587,2	MCF-7	breast:
9	chr4:151233974..151236166-chr4:151243561..151246301,3	K562	blood:
10	chr4:151224130..151227039-chr4:151238410..151241620,3	K562	blood:
11	chr4:151235625..151237717-chr4:151269533..151271331,2	K562	blood:
12	chr4:151274057..151276592-chr4:151280241..151282352,2	K562	blood:
13	chr4:151270468..151272964-chr4:151455945..151457870,2	K562	blood:
14	chr4:151219188..151219691-chr4:151720200..151720886,2	K562	blood:
15	chr4:151315284..151318816-chr4:151320374..151325337,6	K562	blood:
16	chr4:151240646..151243046-chr4:151243526..151245377,2	K562	blood:
17	chr4:151278776..151280327-chr4:151281874..151283378,2	K562	blood:
18	chr4:151218929..151219669-chr4:151787911..151788691,3	K562	blood:
19	chr4:151264691..151267587-chr4:151269891..151271961,2	K562	blood:
20	chr4:151224665..151227039-chr4:151238362..151239910,2	K562	blood:
21	chr4:151275871..151278702-chr4:151280509..151282712,2	K562	blood:
22	chr4:151233974..151240316-chr4:151243440..151247752,8	K562	blood:
23	chr4:151319888..151322699-chr4:151326262..151329136,2	K562	blood:
24	chr4:151240646..151243046-chr4:151243526..151245377,2	K562	blood:
25	chr4:151298940..151301371-chr4:151302683..151304556,2	K562	blood:
26	chr4:151224665..151227039-chr4:151238362..151239910,2	K562	blood:
27	chr4:151235648..151237597-chr4:151263231..151266088,2	K562	blood:
28	chr4:151245581..151248487-chr4:151264731..151266922,2	K562	blood:
29	chr4:151253496..151255758-chr4:151274436..151276149,2	MCF-7	breast:
30	chr4:151315444..151317639-chr4:151319800..151322753,2	MCF-7	breast:
31	chr4:151314752..151316835-chr4:151320252..151322487,2	K562	blood:
32	chr4:151236375..151241361-chr4:151242903..151246234,4	K562	blood:
33	chr4:151289475..151292000-chr4:151297724..151299860,2	K562	blood:
34	chr4:151207253..151208825-chr4:151218908..151221220,2	K562	blood:
35	chr4:151315444..151317639-chr4:151319800..151322753,2	MCF-7	breast:
36	chr4:151323103..151325330-chr4:151403225..151405653,2	K562	blood:
37	chr4:151225266..151228316-chr4:151229626..151232949,5	K562	blood:
38	chr4:151226081..151228552-chr4:151233600..151236243,3	K562	blood:
39	chr4:151269841..151272760-chr4:151278468..151280411,2	K562	blood:
40	chr4:151224130..151227039-chr4:151238410..151241620,3	K562	blood:
41	chr4:151245581..151248487-chr4:151264731..151266922,2	K562	blood:
42	chr4:151269841..151272760-chr4:151278468..151280411,2	K562	blood:
43	chr4:151299346..151301493-chr4:151304266..151307091,2	K562	blood:
44	chr4:151229188..151230723-chr4:151231370..151233714,2	K562	blood:
45	chr4:151267008..151271652-chr4:151273922..151277181,4	K562	blood:
46	chr4:151226081..151228552-chr4:151233600..151236243,3	K562	blood:
47	chr4:151230122..151231763-chr4:151236585..151239256,2	MCF-7	breast:
48	chr4:151299346..151301493-chr4:151304266..151307091,2	K562	blood:
49	chr4:151226356..151227934-chr4:151233600..151235981,2	K562	blood:
50	chr4:151278776..151280327-chr4:151281874..151283378,2	K562	blood:

No data

Variant related genes	Relation type
LRBA	TF binding region
LRBA	CpG island
ENSG00000198589	chromatin interactions

Extended variants
information (count: 3901 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:3901 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10007367	chr4:151214038-151214039	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542601316	chr4:151214052-151214053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370886349	chr4:151214096-151214097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148164610	chr4:151214113-151214114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575849241	chr4:151214133-151214134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544588625	chr4:151214168-151214169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564638390	chr4:151214221-151214222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs71618343	chr4:151214271-151214272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562366830	chr4:151214300-151214301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs17688594	chr4:151214314-151214315	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs191443452	chr4:151214352-151214353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs560559151	chr4:151214360-151214361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142027311	chr4:151214418-151214419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183687647	chr4:151214444-151214445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188739293	chr4:151214467-151214468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73858546	chr4:151214493-151214494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191727539	chr4:151214496-151214497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551406792	chr4:151214505-151214506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571236879	chr4:151214582-151214583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370010278	chr4:151214645-151214646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs117879491	chr4:151214652-151214653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553593412	chr4:151214671-151214672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567022335	chr4:151214687-151214688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368621456	chr4:151214735-151214736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546345849	chr4:151214807-151214808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185408164	chr4:151214812-151214813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs17026803	chr4:151214843-151214844	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs562883109	chr4:151214868-151214869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575964528	chr4:151214898-151214899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544862590	chr4:151214902-151214903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564590677	chr4:151214917-151214918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189986788	chr4:151214939-151214940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182568935	chr4:151214951-151214952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540826422	chr4:151214954-151214955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576446031	chr4:151214993-151214994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543460041	chr4:151215006-151215007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs10010611	chr4:151215019-151215020	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs529345680	chr4:151215022-151215023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557520738	chr4:151215180-151215181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187228685	chr4:151215187-151215188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77569751	chr4:151215189-151215190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551397750	chr4:151215210-151215211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571202151	chr4:151215212-151215213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527630242	chr4:151215247-151215248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548070274	chr4:151215259-151215260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs13121248	chr4:151215263-151215264	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs75114856	chr4:151215284-151215285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35712634	chr4:151215298-151215299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536312246	chr4:151215312-151215313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76964663	chr4:151215337-151215338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Intellectual disability	22102821	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	17588203	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Renal cell carcinoma	20952505	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1202 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:151191400-151245200	Weak transcription	Small Intestine	intestine
2	chr4:151192400-151232800	Weak transcription	Brain Substantia Nigra	brain
3	chr4:151202200-151218000	Weak transcription	Stomach Smooth Muscle	stomach
4	chr4:151202800-151223800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr4:151203600-151218400	Weak transcription	Fetal Stomach	stomach
6	chr4:151203800-151244400	Weak transcription	Fetal Thymus	thymus
7	chr4:151204000-151223800	Weak transcription	K562	blood
8	chr4:151204000-151244600	Weak transcription	Lung	lung
9	chr4:151204600-151216800	Weak transcription	Pancreas	Pancrea
10	chr4:151204600-151236000	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr4:151204600-151242200	Weak transcription	Duodenum Mucosa	Duodenum
12	chr4:151205000-151236400	Weak transcription	Primary B cells from cord blood	blood
13	chr4:151205000-151272200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr4:151206600-151222800	Weak transcription	Osteobl	bone
15	chr4:151206800-151223800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr4:151206800-151223800	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr4:151207200-151226600	Weak transcription	Primary hematopoietic stem cells	blood
18	chr4:151207600-151241600	Weak transcription	Fetal Intestine Large	intestine
19	chr4:151208000-151230400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr4:151208600-151230400	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr4:151210800-151231400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr4:151211200-151227000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr4:151211200-151236200	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr4:151212000-151218400	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr4:151213400-151219000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr4:151213400-151229000	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr4:151213400-151242200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr4:151213600-151226600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr4:151213600-151231000	Weak transcription	Primary T cells from cord blood	blood
30	chr4:151213800-151222800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr4:151213800-151236200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:151218200-151220000	Enhancers	Rectal Smooth Muscle	rectum
33	chr4:151218400-151218600	Enhancers	Fetal Stomach	stomach
34	chr4:151218400-151219200	Enhancers	Colon Smooth Muscle	Colon
35	chr4:151218400-151219800	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr4:151219200-151219400	Flanking Active TSS	Colon Smooth Muscle	Colon
37	chr4:151219400-151220000	Active TSS	Colon Smooth Muscle	Colon
38	chr4:151219600-151219800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr4:151219800-151221200	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr4:151219800-151222800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr4:151220000-151220800	Weak transcription	Colon Smooth Muscle	Colon
42	chr4:151220000-151221400	Weak transcription	Rectal Smooth Muscle	rectum
43	chr4:151220800-151221200	Enhancers	Colon Smooth Muscle	Colon
44	chr4:151221200-151221800	Active TSS	Duodenum Smooth Muscle	Duodenum
45	chr4:151221200-151222800	Active TSS	Colon Smooth Muscle	Colon
46	chr4:151221400-151222000	Active TSS	Rectal Smooth Muscle	rectum
47	chr4:151221800-151231200	Weak transcription	Fetal Heart	heart
48	chr4:151221800-151236200	Weak transcription	Left Ventricle	heart
49	chr4:151221800-151259600	Weak transcription	Fetal Intestine Small	intestine
50	chr4:151222000-151222600	Weak transcription	Rectal Smooth Muscle	rectum

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