Variant report

Variant	nsv818171
Chromosome Location	chr3:142894411-142960273
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:568)
CpG islands
(count:244)
Chromatin interactive
region (count:73)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:568 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:142900853-142901159	K562	blood:	n/a	n/a
2	ARID3A	chr3:142897049-142897053	K562	blood:	n/a	n/a
3	ARID3A	chr3:142902142-142902812	K562	blood:	n/a	n/a
4	ATF1	chr3:142896868-142897147	K562	blood:	n/a	n/a
5	ATF2	chr3:142899282-142899641	GM12878	blood:	n/a	n/a
6	ATF2	chr3:142925940-142926781	GM12878	blood:	n/a	n/a
7	ATF2	chr3:142926094-142926643	GM12878	blood:	n/a	n/a
8	ATF3	chr3:142941383-142941722	K562	blood:	n/a	n/a
9	BACH1	chr3:142926223-142926583	K562	blood:	n/a	n/a
10	BACH1	chr3:142926292-142926562	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr3:142896728-142896940	GM12878	blood:	n/a	n/a
12	BATF	chr3:142926120-142926589	GM12878	blood:	n/a	n/a
13	BATF	chr3:142896967-142897183	GM12878	blood:	n/a	chr3:142897061-142897072
14	BATF	chr3:142896975-142897185	GM12878	blood:	n/a	chr3:142897061-142897072
15	BCL11A	chr3:142896930-142897147	GM12878	blood:	n/a	n/a
16	BCL11A	chr3:142926100-142926557	GM12878	blood:	n/a	n/a
17	BCL11A	chr3:142926060-142926545	GM12878	blood:	n/a	n/a
18	BCL3	chr3:142925964-142926581	GM12878	blood:	n/a	n/a
19	BCLAF1	chr3:142925723-142926725	GM12878	blood:	n/a	n/a
20	BCLAF1	chr3:142926050-142926724	GM12878	blood:	n/a	n/a
21	BHLHE40	chr3:142926070-142926539	GM12878	blood:	n/a	n/a
22	BHLHE40	chr3:142941367-142941680	K562	blood:	n/a	n/a
23	CBX3	chr3:142911803-142912166	K562	blood:	n/a	n/a
24	CBX3	chr3:142902085-142903026	K562	blood:	n/a	n/a
25	CBX3	chr3:142914454-142914881	K562	blood:	n/a	n/a
26	CBX3	chr3:142896742-142897236	K562	blood:	n/a	n/a
27	CBX3	chr3:142941254-142941740	K562	blood:	n/a	n/a
28	CCNT2	chr3:142941447-142941639	K562	blood:	n/a	n/a
29	CCNT2	chr3:142936308-142936485	K562	blood:	n/a	n/a
30	CCNT2	chr3:142902198-142902830	K562	blood:	n/a	chr3:142902508-142902528
31	CCNT2	chr3:142900846-142901134	K562	blood:	n/a	n/a
32	CEBPB	chr3:142901955-142902272	HepG2	liver:	n/a	chr3:142902094-142902105
33	CEBPB	chr3:142926250-142926475	K562	blood:	n/a	n/a
34	CEBPB	chr3:142901955-142902263	Hela-S3	cervix:	n/a	chr3:142902094-142902105
35	CEBPB	chr3:142955043-142955384	A549	lung:	n/a	n/a
36	CEBPB	chr3:142901952-142902282	IMR90	lung:	n/a	chr3:142902094-142902105
37	CEBPB	chr3:142935848-142936007	K562	blood:	n/a	n/a
38	CEBPB	chr3:142955117-142955317	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr3:142901970-142902260	A549	lung:	n/a	chr3:142902094-142902105
40	CEBPB	chr3:142898166-142898282	HepG2	liver:	n/a	n/a
41	CEBPB	chr3:142955065-142955364	K562	blood:	n/a	n/a
42	CEBPB	chr3:142898261-142898325	K562	blood:	n/a	n/a
43	CEBPB	chr3:142925702-142926597	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr3:142901738-142902685	K562	blood:	n/a	chr3:142902094-142902105
45	CEBPB	chr3:142935866-142935999	A549	lung:	n/a	n/a
46	CEBPB	chr3:142902017-142902206	H1-hESC	embryonic stem cell:	n/a	chr3:142902094-142902105
47	CEBPB	chr3:142926148-142926583	ECC-1	luminal epithelium:	n/a	n/a
48	CEBPB	chr3:142933725-142934108	HepG2	liver:	n/a	chr3:142934047-142934060 chr3:142933823-142933834
49	CEBPB	chr3:142923465-142923583	K562	blood:	n/a	n/a
50	CEBPB	chr3:142933743-142934071	A549	lung:	n/a	chr3:142934047-142934060 chr3:142933823-142933834

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:142895861-142895911	AG04449	skin:	fetal
2	chr3:142895375-142895425	ovcar-3	ovarian:	n/a
3	chr3:142895861-142895911	CMK	blood:	n/a
4	chr3:142926178-142926228	NHBE	bronchial:	n/a
5	chr3:142895375-142895425	HMEC	breast:	n/a
6	chr3:142895375-142895425	SK-N-SH_RA	brain:	n/a
7	chr3:142895861-142895911	Caco-2	colon:	n/a
8	chr3:142926178-142926228	GM12892	blood:	n/a
9	chr3:142895279-142895329	Hepatocyte	liver:	n/a
10	chr3:142895279-142895329	AG04449	skin:	fetal
11	chr3:142926178-142926228	U87	brain:	n/a
12	chr3:142895375-142895425	HEK293	kidney:	embryo
13	chr3:142895375-142895425	Caco-2	colon:	n/a
14	chr3:142926178-142926228	PFSK-1	brain:	n/a
15	chr3:142895279-142895329	HEK293	kidney:	embryo
16	chr3:142895861-142895911	Hepatocyte	liver:	n/a
17	chr3:142926178-142926228	GM06990	blood:	n/a
18	chr3:142895375-142895425	AG10803	skin:	n/a
19	chr3:142895375-142895425	GM19239	blood:	n/a
20	chr3:142895861-142895911	SAEC	small airway:	n/a
21	chr3:142926178-142926228	NB4	blood:	n/a
22	chr3:142895279-142895329	K562	blood:	n/a
23	chr3:142895279-142895329	U87	brain:	n/a
24	chr3:142895375-142895425	CMK	blood:	n/a
25	chr3:142926178-142926228	T-47D	breast:	n/a
26	chr3:142926178-142926228	CMK	blood:	n/a
27	chr3:142895375-142895425	SKMC	muscle:	n/a
28	chr3:142895279-142895329	H1-hESC	embryonic stem cell:	embryo
29	chr3:142926178-142926228	HL-60	blood:	n/a
30	chr3:142895861-142895911	T-47D	breast:	n/a
31	chr3:142895279-142895329	SK-N-MC	brain:	n/a
32	chr3:142895375-142895425	AG04450	lung:	fetal
33	chr3:142895375-142895425	GM12878	blood:	n/a
34	chr3:142926178-142926228	ProgFib	skin:	n/a
35	chr3:142895375-142895425	NB4	blood:	n/a
36	chr3:142895861-142895911	HPAEpiC	pulmonary alveolar:	n/a
37	chr3:142895279-142895329	BJ	skin:	n/a
38	chr3:142895279-142895329	NHBE	bronchial:	n/a
39	chr3:142895279-142895329	Hela-S3	cervix:	n/a
40	chr3:142895279-142895329	AG10803	skin:	n/a
41	chr3:142895861-142895911	AG09309	skin:	n/a
42	chr3:142895861-142895911	A549	lung:	n/a
43	chr3:142895861-142895911	LNCaP	prostate:	n/a
44	chr3:142895279-142895329	GM06990	blood:	n/a
45	chr3:142895279-142895329	AG04450	lung:	fetal
46	chr3:142926178-142926228	HPAEpiC	pulmonary alveolar:	n/a
47	chr3:142926178-142926228	NHDF-neo	bronchial:	n/a
48	chr3:142895279-142895329	HEEpiC	esophagus:	n/a
49	chr3:142926178-142926228	HNPCEpiC	eye:	n/a
50	chr3:142895861-142895911	GM06990	blood:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:142933374..142937118-chr3:142939813..142945037,5	K562	blood:
2	chr3:142883459..142885076-chr3:142902502..142904668,2	K562	blood:
3	chr3:142930578..142932212-chr3:142932647..142934719,2	K562	blood:
4	chr3:142908825..142914026-chr3:142914356..142919906,7	K562	blood:
5	chr3:142907861..142909717-chr3:142911559..142913814,2	K562	blood:
6	chr3:142842312..142844525-chr3:142920222..142922927,2	K562	blood:
7	chr3:142900165..142901896-chr3:142950119..142953076,2	K562	blood:
8	chr3:142837172..142841368-chr3:142932749..142935572,3	K562	blood:
9	chr3:142914308..142916627-chr3:142918947..142921480,2	K562	blood:
10	chr3:142899439..142901462-chr3:142905793..142908005,2	K562	blood:
11	chr3:142917669..142921522-chr3:142924910..142927664,3	K562	blood:
12	chr3:142875650..142878540-chr3:142902217..142903747,2	K562	blood:
13	chr3:142914308..142916627-chr3:142918947..142921480,2	K562	blood:
14	chr3:142922192..142925185-chr3:142931380..142934358,2	K562	blood:
15	chr3:142948047..142951312-chr3:142952653..142957193,4	K562	blood:
16	chr3:142901683..142905677-chr3:142909688..142913196,5	K562	blood:
17	chr3:142930578..142932212-chr3:142932647..142934719,2	K562	blood:
18	chr3:142907021..142910266-chr3:142911152..142913564,3	K562	blood:
19	chr3:142940072..142941625-chr3:142954271..142955900,2	K562	blood:
20	chr3:142938475..142939430-chr3:142950578..142951319,2	MCF-7	breast:
21	chr3:142935120..142937637-chr3:142937877..142939570,2	MCF-7	breast:
22	chr3:142940072..142941625-chr3:142954271..142955900,2	K562	blood:
23	chr3:142955679..142958275-chr3:142964132..142966713,2	K562	blood:
24	chr3:142918300..142920442-chr3:142921412..142923086,3	K562	blood:
25	chr3:142921678..142924452-chr3:142925121..142926893,2	K562	blood:
26	chr3:142947986..142949747-chr3:143028626..143030178,2	K562	blood:
27	chr3:142901683..142905677-chr3:142909688..142913196,5	K562	blood:
28	chr3:142929546..142932145-chr3:142933219..142936261,3	K562	blood:
29	chr3:142917101..142918800-chr3:142923414..142925582,2	K562	blood:
30	chr3:142951962..142955904-chr3:142971401..142974768,3	K562	blood:
31	chr3:142918300..142920442-chr3:142921412..142923086,3	K562	blood:
32	chr3:142889235..142895118-chr3:142897231..142901814,7	K562	blood:
33	chr3:142889235..142895118-chr3:142897231..142901814,7	K562	blood:
34	chr3:142918145..142921332-chr3:143025862..143029822,3	K562	blood:
35	chr3:142956744..142958765-chr3:142965944..142967632,2	K562	blood:
36	chr3:142910443..142912503-chr3:142926393..142928620,2	K562	blood:
37	chr3:142921678..142924452-chr3:142925121..142926893,2	K562	blood:
38	chr3:142746681..142748663-chr3:142941428..142944295,2	K562	blood:
39	chr3:142933374..142937118-chr3:142939813..142945037,5	K562	blood:
40	chr3:142917101..142918800-chr3:142923414..142925582,2	K562	blood:
41	chr3:142837194..142839590-chr3:142902275..142903779,2	K562	blood:
42	chr3:142938475..142939430-chr3:142950578..142951319,2	MCF-7	breast:
43	chr3:142918300..142920057-chr3:142921412..142923080,2	K562	blood:
44	chr3:142904057..142907019-chr3:142910125..142912001,3	K562	blood:
45	chr3:142945884..142947891-chr3:142949125..142952561,4	K562	blood:
46	chr3:142899439..142901462-chr3:142905793..142908005,2	K562	blood:
47	chr3:142948047..142951312-chr3:142952653..142957193,4	K562	blood:
48	chr3:142925537..142928123-chr3:142932131..142934327,2	K562	blood:
49	chr3:142949903..142951935-chr3:143002034..143003795,2	K562	blood:
50	chr3:142926220..142927861-chr3:142959735..142962076,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHST2-10	chr3:142951419-142951544	l_2486_chr3:142951418-142976230_ovary
2	lnc-CHST2-10	chr3:142951611-142951872	l_2486_chr3:142951418-142976230_ovary

No data

Variant related genes	Relation type
PBX2P1	TF binding region
PBX2P1	CpG island
ENSG00000175040	chromatin interactions
ENSG00000211483	chromatin interactions

Extended variants
information (count: 2562 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2562 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs894177	chr3:142894411-142894412	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs367857660	chr3:142894414-142894415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144221453	chr3:142894422-142894423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545087780	chr3:142894482-142894483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563292525	chr3:142894547-142894548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553944927	chr3:142894553-142894554	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184149822	chr3:142894592-142894593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528831541	chr3:142894593-142894594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542628580	chr3:142894655-142894656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372162649	chr3:142894689-142894690	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs189531761	chr3:142894729-142894730	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs528778928	chr3:142894754-142894755	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs546881696	chr3:142894768-142894769	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs148310842	chr3:142894829-142894830	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs192830460	chr3:142894838-142894839	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs185178034	chr3:142894915-142894916	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs568994619	chr3:142894931-142894932	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs142031109	chr3:142894953-142894954	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs554947866	chr3:142894965-142894966	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs112853059	chr3:142894982-142894983	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs11928437	chr3:142895003-142895004	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs375521183	chr3:142895026-142895027	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs539814250	chr3:142895031-142895032	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs113832906	chr3:142895054-142895055	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs527351438	chr3:142895060-142895061	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs369891159	chr3:142895066-142895067	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs190108894	chr3:142895077-142895078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577882035	chr3:142895086-142895087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545200097	chr3:142895089-142895090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs62276939	chr3:142895117-142895118	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs575400234	chr3:142895121-142895122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs61032856	chr3:142895132-142895133	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs373179673	chr3:142895155-142895156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs3927028	chr3:142895174-142895175	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs528790577	chr3:142895181-142895182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540892678	chr3:142895193-142895194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565418740	chr3:142895210-142895211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533999492	chr3:142895211-142895212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532603815	chr3:142895217-142895218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550753432	chr3:142895244-142895245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562690284	chr3:142895280-142895281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530091319	chr3:142895293-142895294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548304833	chr3:142895296-142895297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs894178	chr3:142895298-142895299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534631212	chr3:142895361-142895362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377670166	chr3:142895364-142895365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546899544	chr3:142895389-142895390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571548762	chr3:142895396-142895397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369264843	chr3:142895439-142895440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557189529	chr3:142895449-142895450	Weak transcription	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
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Cancer	20164919	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:626 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142891600-142894800	Enhancers	Primary T cells from cord blood	blood
2	chr3:142891600-142897000	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr3:142891800-142894600	Enhancers	Fetal Thymus	thymus
4	chr3:142891800-142894800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr3:142892000-142898400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr3:142893000-142894800	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr3:142893200-142909200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr3:142894000-142894600	Enhancers	Thymus	Thymus
9	chr3:142894200-142894800	Enhancers	Dnd41	blood
10	chr3:142894200-142900200	Weak transcription	GM12878-XiMat	blood
11	chr3:142894400-142897800	Weak transcription	Fetal Lung	lung
12	chr3:142894400-142898400	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr3:142894400-142898400	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr3:142894400-142898400	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr3:142894400-142899600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr3:142894400-142900800	Weak transcription	K562	blood
17	chr3:142894800-142896200	Weak transcription	Dnd41	blood
18	chr3:142894800-142898200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr3:142894800-142898400	Weak transcription	Primary T cells from cord blood	blood
20	chr3:142896200-142896800	Enhancers	Dnd41	blood
21	chr3:142896800-142898200	Weak transcription	Dnd41	blood
22	chr3:142896800-142898800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr3:142897000-142898800	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr3:142897800-142898800	Enhancers	Fetal Lung	lung
25	chr3:142898200-142898800	Enhancers	Dnd41	blood
26	chr3:142898200-142899000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr3:142898400-142898600	Enhancers	Primary T cells from cord blood	blood
28	chr3:142898400-142898600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr3:142898400-142898600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr3:142898400-142898800	Enhancers	Primary T cells fromperipheralblood	blood
31	chr3:142898400-142898800	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr3:142898400-142898800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr3:142898400-142899000	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr3:142898400-142899000	Enhancers	Fetal Thymus	thymus
35	chr3:142898600-142901600	Weak transcription	Primary T cells from cord blood	blood
36	chr3:142898800-142900000	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr3:142898800-142900600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr3:142898800-142901200	Weak transcription	Dnd41	blood
39	chr3:142898800-142901800	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr3:142898800-142902200	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr3:142899000-142901600	Weak transcription	Fetal Thymus	thymus
42	chr3:142899000-142902200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr3:142899000-142902400	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr3:142899400-142902000	Enhancers	Primary B cells from peripheral blood	blood
45	chr3:142899600-142900000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr3:142900000-142901600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr3:142900000-142902000	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr3:142900200-142901000	ZNF genes & repeats	GM12878-XiMat	blood
49	chr3:142900200-142903400	Enhancers	Primary hematopoietic stem cells	blood
50	chr3:142900400-142901800	Enhancers	Primary B cells from cord blood	blood

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