Variant report

Variant	nsv877564
Chromosome Location	chr3:143059952-143116883
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:348)
CpG islands
(count:61)
Chromatin interactive
region (count:46)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:143085532-143085796	K562	blood:	n/a	n/a
2	ATF1	chr3:143085572-143086036	K562	blood:	n/a	n/a
3	BACH1	chr3:143067696-143068015	K562	blood:	n/a	n/a
4	BACH1	chr3:143064835-143064841	K562	blood:	n/a	n/a
5	BATF	chr3:143068346-143068628	GM12878	blood:	n/a	chr3:143068504-143068515
6	BHLHE40	chr3:143067572-143068180	K562	blood:	n/a	n/a
7	BHLHE40	chr3:143085702-143085825	K562	blood:	n/a	n/a
8	CBX3	chr3:143099970-143100368	K562	blood:	n/a	n/a
9	CBX3	chr3:143067547-143068118	K562	blood:	n/a	n/a
10	CEBPB	chr3:143094498-143094735	K562	blood:	n/a	n/a
11	CEBPB	chr3:143067323-143068013	K562	blood:	n/a	chr3:143067514-143067527 chr3:143067516-143067525 chr3:143067516-143067525 chr3:143067514-143067527 chr3:143067516-143067525 chr3:143067516-143067525
12	CEBPB	chr3:143073044-143073244	A549	lung:	n/a	n/a
13	CEBPB	chr3:143067346-143067754	K562	blood:	n/a	chr3:143067514-143067527 chr3:143067516-143067525 chr3:143067516-143067525 chr3:143067514-143067527 chr3:143067516-143067525 chr3:143067516-143067525
14	CEBPB	chr3:143067388-143067664	IMR90	lung:	n/a	chr3:143067514-143067527 chr3:143067516-143067525 chr3:143067516-143067525 chr3:143067514-143067527 chr3:143067516-143067525 chr3:143067516-143067525
15	CEBPB	chr3:143097592-143097840	HepG2	liver:	n/a	chr3:143097712-143097723
16	CEBPD	chr3:143085512-143085887	K562	blood:	n/a	n/a
17	CTCF	chr3:143067940-143068090	HAc	cerebellar:	n/a	n/a
18	CTCF	chr3:143067880-143068030	GM12878	blood:	n/a	n/a
19	CTCF	chr3:143067867-143068031	GM19239	blood:	n/a	n/a
20	CTCF	chr3:143067860-143068010	GM12866	blood:	n/a	n/a
21	CTCF	chr3:143067660-143067810	HFF-Myc	foreskin:	n/a	n/a
22	CTCF	chr3:143067880-143068030	K562	blood:	n/a	n/a
23	CTCF	chr3:143067868-143068044	GM19240	blood:	n/a	n/a
24	CTCF	chr3:143067800-143067950	GM12870	blood:	n/a	n/a
25	CTCF	chr3:143067840-143067990	Caco-2	colon:	n/a	n/a
26	CTCF	chr3:143067880-143068030	HL-60	blood:	n/a	n/a
27	CTCF	chr3:143067876-143068044	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr3:143067819-143068102	K562	blood:	n/a	n/a
29	CTCF	chr3:143067880-143068030	GM12801	blood:	n/a	n/a
30	CTCF	chr3:143067880-143068030	HCM	heart:	n/a	n/a
31	CTCF	chr3:143067880-143068030	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr3:143067920-143068070	HPF	lung:	n/a	n/a
33	CTCF	chr3:143067880-143068030	GM12864	blood:	n/a	n/a
34	CTCF	chr3:143067880-143068030	HRE	kidney:	n/a	n/a
35	CTCF	chr3:143085640-143085790	GM12864	blood:	n/a	chr3:143085748-143085756
36	CTCF	chr3:143067860-143068010	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr3:143085660-143085815	K562	blood:	n/a	chr3:143085748-143085756
38	CTCF	chr3:143067920-143068070	HAc	cerebellar:	n/a	n/a
39	CTCF	chr3:143067900-143068050	GM12872	blood:	n/a	n/a
40	CTCF	chr3:143067920-143068070	GM12870	blood:	n/a	n/a
41	CTCF	chr3:143085660-143085810	HCPEpiC	choroid plexus:	n/a	chr3:143085748-143085756
42	CTCF	chr3:143067900-143068050	GM12878	blood:	n/a	n/a
43	CTCF	chr3:143067840-143067990	HEK293	kidney:	n/a	n/a
44	CTCF	chr3:143067880-143068030	GM12875	blood:	n/a	n/a
45	CTCF	chr3:143067881-143067999	GM10266	blood:	n/a	n/a
46	CTCF	chr3:143067860-143068010	NB4	blood:	n/a	n/a
47	CTCF	chr3:143067883-143068029	MCF-7	breast:	n/a	n/a
48	CTCF	chr3:143067871-143068032	Fibrobl	skin:	n/a	n/a
49	CTCF	chr3:143067880-143068030	GM12868	blood:	n/a	n/a
50	CTCF	chr3:143067740-143067890	WI-38	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:143097071-143097121	HEK293	kidney:	embryo
2	chr3:143097071-143097121	BE2_C	brain:	n/a
3	chr3:143097071-143097121	Hela-S3	cervix:	n/a
4	chr3:143097071-143097121	HNPCEpiC	eye:	n/a
5	chr3:143097071-143097121	SAEC	small airway:	n/a
6	chr3:143097071-143097121	AG04449	skin:	fetal
7	chr3:143097071-143097121	AG09319	gingival:	n/a
8	chr3:143097071-143097121	HEEpiC	esophagus:	n/a
9	chr3:143097071-143097121	HMEC	breast:	n/a
10	chr3:143097071-143097121	AG04450	lung:	fetal
11	chr3:143097071-143097121	GM19239	blood:	n/a
12	chr3:143097071-143097121	NT2-D1	testis:	n/a
13	chr3:143097071-143097121	GM12892	blood:	n/a
14	chr3:143097071-143097121	HRE	kidney:	n/a
15	chr3:143097071-143097121	Jurkat	blood:	n/a
16	chr3:143097071-143097121	NH-A	brain:	n/a
17	chr3:143097071-143097121	HRPEpiC	eye:	n/a
18	chr3:143097071-143097121	SK-N-MC	brain:	n/a
19	chr3:143097071-143097121	HUVEC	blood vessel:	n/a
20	chr3:143097071-143097121	PFSK-1	brain:	n/a
21	chr3:143097071-143097121	PANC-1	pancreas:	n/a
22	chr3:143097071-143097121	NHBE	bronchial:	n/a
23	chr3:143097071-143097121	ProgFib	skin:	n/a
24	chr3:143097071-143097121	T-47D	breast:	n/a
25	chr3:143097071-143097121	CMK	blood:	n/a
26	chr3:143097071-143097121	U87	brain:	n/a
27	chr3:143097071-143097121	LNCaP	prostate:	n/a
28	chr3:143097071-143097121	SK-N-SH	brain:	n/a
29	chr3:143097071-143097121	NB4	blood:	n/a
30	chr3:143097071-143097121	HepG2	liver:	n/a
31	chr3:143097071-143097121	AoSMC	blood vessel:	n/a
32	chr3:143097071-143097121	HCF	heart:	n/a
33	chr3:143097071-143097121	NHDF-neo	bronchial:	n/a
34	chr3:143097071-143097121	Caco-2	colon:	n/a
35	chr3:143097071-143097121	Hepatocyte	liver:	n/a
36	chr3:143097071-143097121	HPAEpiC	pulmonary alveolar:	n/a
37	chr3:143097071-143097121	SKMC	muscle:	n/a
38	chr3:143097071-143097121	AG09309	skin:	n/a
39	chr3:143097071-143097121	HIPEpiC	eye:	n/a
40	chr3:143097071-143097121	MCF10A-Er-Src	breast:	n/a
41	chr3:143097071-143097121	K562	blood:	n/a
42	chr3:143097071-143097121	H1-hESC	embryonic stem cell:	embryo
43	chr3:143097071-143097121	GM12891	blood:	n/a
44	chr3:143097071-143097121	AG10803	skin:	n/a
45	chr3:143097071-143097121	A549	lung:	n/a
46	chr3:143097071-143097121	MCF-7	breast:	n/a
47	chr3:143097071-143097121	GM12878	blood:	n/a
48	chr3:143097071-143097121	ECC-1	luminal epithelium:	n/a
49	chr3:143097071-143097121	RPTEC	kidney:	n/a
50	chr3:143097071-143097121	BJ	skin:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:143089798..143091848-chr3:143094330..143096533,2	K562	blood:
2	chr3:143070031..143071586-chr3:143073564..143076244,2	K562	blood:
3	chr3:143073365..143075780-chr3:143077862..143079884,2	K562	blood:
4	chr3:143073365..143075780-chr3:143077862..143079884,2	K562	blood:
5	chr3:143083767..143087407-chr3:143088395..143091311,3	K562	blood:
6	chr3:143081768..143084316-chr3:143087882..143089415,2	MCF-7	breast:
7	chr3:143071861..143075412-chr3:143075859..143077751,4	K562	blood:
8	chr3:143070031..143071586-chr3:143073564..143076244,2	K562	blood:
9	chr3:143047197..143050151-chr3:143065282..143067644,2	K562	blood:
10	chr3:143061262..143062878-chr3:143065854..143067728,2	K562	blood:
11	chr3:143089798..143091848-chr3:143094330..143096533,2	K562	blood:
12	chr3:143063232..143067878-chr3:143069249..143072270,4	K562	blood:
13	chr3:143071861..143075412-chr3:143075859..143077751,4	K562	blood:
14	chr3:143061262..143062878-chr3:143065854..143067728,2	K562	blood:
15	chr3:143057632..143059854-chr3:143064608..143066559,2	K562	blood:
16	chr3:142835479..142837341-chr3:143085961..143087735,2	K562	blood:
17	chr3:143075166..143076875-chr3:143081187..143082787,2	K562	blood:
18	chr3:143068671..143071346-chr3:143094512..143096094,2	K562	blood:
19	chr3:143064715..143066302-chr3:143076677..143078455,2	K562	blood:
20	chr3:143073351..143075780-chr3:143076251..143080121,5	K562	blood:
21	chr3:143099826..143101455-chr3:143101968..143104391,2	K562	blood:
22	chr3:143049101..143052451-chr3:143056626..143059965,3	K562	blood:
23	chr3:143075166..143076875-chr3:143081187..143082787,2	K562	blood:
24	chr3:143068671..143071346-chr3:143094512..143096094,2	K562	blood:
25	chr3:143067407..143070275-chr3:143070777..143072704,2	K562	blood:
26	chr3:142839497..142841574-chr3:143081300..143083347,2	K562	blood:
27	chr3:143067819..143069970-chr3:143072311..143075469,3	K562	blood:
28	chr3:143076644..143082089-chr3:143083976..143087336,5	K562	blood:
29	chr3:143076644..143082089-chr3:143083976..143087336,5	K562	blood:
30	chr3:143107077..143109366-chr3:143114729..143117403,2	K562	blood:
31	chr3:143081768..143084316-chr3:143087882..143089415,2	MCF-7	breast:
32	chr3:143067407..143070275-chr3:143070777..143072704,2	K562	blood:
33	chr3:143067819..143069970-chr3:143072311..143075469,3	K562	blood:
34	chr3:143079326..143082089-chr3:143083976..143087226,3	K562	blood:
35	chr3:143094103..143096377-chr3:143119769..143122751,2	K562	blood:
36	chr3:143054747..143057331-chr3:143064098..143066734,2	K562	blood:
37	chr3:143073351..143075780-chr3:143076251..143080121,5	K562	blood:
38	chr3:143083767..143087407-chr3:143088395..143091311,3	K562	blood:
39	chr3:142841472..142843764-chr3:143071795..143073480,2	K562	blood:
40	chr3:143107077..143109366-chr3:143114729..143117403,2	K562	blood:
41	chr3:143106712..143109351-chr3:143117570..143120299,2	K562	blood:
42	chr3:143064715..143066302-chr3:143076677..143078455,2	K562	blood:
43	chr3:143032733..143035249-chr3:143069425..143071800,2	K562	blood:
44	chr3:143063232..143067878-chr3:143069249..143072270,4	K562	blood:
45	chr3:142838518..142840970-chr3:143064617..143066302,2	K562	blood:
46	chr3:143079326..143082089-chr3:143083976..143087226,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHST2-3	chr3:143062192-143062456	ENSG00000240012.1
2	lnc-CHST2-3	chr3:143065828-143065913	ENSG00000240012.1
3	lnc-CHST2-3	chr3:143061088-143061126	ENSG00000240012.1
4	lnc-CHST2-3	chr3:143063309-143063436	ENSG00000240012.1
5	lnc-CHST2-4	chr3:143100786-143101003	ENSG00000244493.1
6	lnc-CHST2-4	chr3:143100180-143100288	ENSG00000244493.1

No data

Variant related genes	Relation type
SLC9A9-AS1	TF binding region
SLC9A9-AS2	TF binding region
SLC9A9-AS1	CpG island
SLC9A9-AS2	CpG island
ENSG00000240888	chromatin interactions
ENSG00000241679	chromatin interactions
ENSG00000244493	chromatin interactions

Extended variants
information (count: 2221 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2221 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1501629	chr3:143059952-143059953	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547354738	chr3:143059962-143059963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369208907	chr3:143059975-143059976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543013020	chr3:143059984-143059985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565760418	chr3:143060013-143060014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs180889520	chr3:143060014-143060015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144956727	chr3:143060023-143060024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559279173	chr3:143060050-143060051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185880219	chr3:143060051-143060052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4263260	chr3:143060113-143060114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544714671	chr3:143060122-143060123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562998803	chr3:143060142-143060143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539501530	chr3:143060146-143060147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191523272	chr3:143060147-143060148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530447360	chr3:143060164-143060165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557839311	chr3:143060180-143060181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182984385	chr3:143060182-143060183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149079131	chr3:143060228-143060229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561663529	chr3:143060257-143060258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs1501628	chr3:143060272-143060273	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs547221016	chr3:143060303-143060304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571754953	chr3:143060334-143060335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539186711	chr3:143060355-143060356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551113625	chr3:143060383-143060384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs386666574	chr3:143060386-143060387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201766594	chr3:143060387-143060388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555761968	chr3:143060404-143060405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536678398	chr3:143060407-143060408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369856459	chr3:143060424-143060425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188817820	chr3:143060451-143060452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573923710	chr3:143060457-143060458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4839590	chr3:143060464-143060465	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs553194002	chr3:143060486-143060487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs143155369	chr3:143060487-143060488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572136255	chr3:143060532-143060533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544777152	chr3:143060567-143060568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115170806	chr3:143060622-143060623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs148269871	chr3:143060632-143060633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141302902	chr3:143060673-143060674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560721564	chr3:143060684-143060685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528823990	chr3:143060695-143060696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542864615	chr3:143060783-143060784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540265445	chr3:143060785-143060786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191615250	chr3:143060786-143060787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541046960	chr3:143060787-143060788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182860798	chr3:143060793-143060794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373152328	chr3:143060815-143060816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs187985013	chr3:143060824-143060825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376495703	chr3:143060826-143060827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs147010582	chr3:143060835-143060836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	22522925	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143049200-143061200	Weak transcription	Fetal Thymus	thymus
2	chr3:143052600-143061600	Weak transcription	Dnd41	blood
3	chr3:143056800-143062400	Weak transcription	Primary T cells from cord blood	blood
4	chr3:143060200-143062600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr3:143060800-143061000	Enhancers	Psoas Muscle	Psoas
6	chr3:143061000-143061800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr3:143061200-143062400	Enhancers	Fetal Thymus	thymus
8	chr3:143061400-143063600	Enhancers	HUVEC	blood vessel
9	chr3:143061400-143064000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr3:143061600-143064200	Enhancers	Dnd41	blood
11	chr3:143061800-143062600	Enhancers	Brain Angular Gyrus	brain
12	chr3:143061800-143066800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr3:143062000-143062200	Enhancers	Primary T helper cells PMA-I stimulated	--
14	chr3:143062000-143062400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr3:143062200-143063800	Weak transcription	Primary T helper cells PMA-I stimulated	--
16	chr3:143062400-143062800	Enhancers	Brain Hippocampus Middle	brain
17	chr3:143062400-143063600	Enhancers	Brain Substantia Nigra	brain
18	chr3:143062400-143064400	Enhancers	Primary T cells from cord blood	blood
19	chr3:143062400-143065800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr3:143062400-143066400	Weak transcription	Fetal Thymus	thymus
21	chr3:143062600-143063000	Enhancers	Brain Anterior Caudate	brain
22	chr3:143062600-143063400	Weak transcription	Brain Angular Gyrus	brain
23	chr3:143062600-143064200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr3:143063000-143063200	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr3:143063000-143063400	Weak transcription	Brain Anterior Caudate	brain
26	chr3:143063200-143066400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr3:143063400-143063600	Enhancers	Brain Angular Gyrus	brain
28	chr3:143063400-143063600	Enhancers	Brain Anterior Caudate	brain
29	chr3:143063400-143064000	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr3:143063600-143064000	Flanking Active TSS	HUVEC	blood vessel
31	chr3:143063600-143064400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr3:143063600-143076400	Weak transcription	Brain Anterior Caudate	brain
33	chr3:143063800-143064600	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr3:143064000-143065000	Enhancers	HUVEC	blood vessel
35	chr3:143064000-143067000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr3:143064000-143067200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr3:143064200-143064400	Flanking Active TSS	Dnd41	blood
38	chr3:143064200-143064400	Enhancers	K562	blood
39	chr3:143064200-143064600	Enhancers	Ovary	ovary
40	chr3:143064200-143067000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr3:143064400-143065800	Weak transcription	Primary T cells from cord blood	blood
42	chr3:143064400-143066600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr3:143064400-143067400	Weak transcription	K562	blood
44	chr3:143064400-143068400	Enhancers	Dnd41	blood
45	chr3:143064600-143066000	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr3:143064600-143070800	Weak transcription	Ovary	ovary
47	chr3:143065800-143067400	Enhancers	Primary T cells from cord blood	blood
48	chr3:143065800-143067400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
49	chr3:143066000-143069000	Enhancers	Primary T helper cells PMA-I stimulated	--
50	chr3:143066200-143069200	Enhancers	Primary T helper cells fromperipheralblood	blood

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