Variant report

Variant	nsv999000
Chromosome Location	chr3:143086325-143136128
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:143130746-143131359	GM12878	blood:	n/a	n/a
2	BATF	chr3:143133523-143133818	GM12878	blood:	n/a	n/a
3	CBX3	chr3:143099970-143100368	K562	blood:	n/a	n/a
4	CEBPB	chr3:143097592-143097840	HepG2	liver:	n/a	chr3:143097712-143097723
5	CEBPB	chr3:143094498-143094735	K562	blood:	n/a	n/a
6	CTCF	chr3:143106720-143106870	K562	blood:	n/a	chr3:143106829-143106842 chr3:143106830-143106840 chr3:143106827-143106845
7	CTCF	chr3:143106840-143106990	Caco-2	colon:	n/a	n/a
8	CTCF	chr3:143106832-143106838	K562	blood:	n/a	n/a
9	CTCF	chr3:143114353-143114416	Kidney_OC	kidney:	n/a	n/a
10	CTCF	chr3:143100176-143100217	Spleen_OC	spleen:	n/a	n/a
11	CTCF	chr3:143106778-143106874	HUVEC	blood vessel:	n/a	chr3:143106829-143106842 chr3:143106830-143106840 chr3:143106827-143106845
12	CTCF	chr3:143107854-143107906	GM13976	blood:	n/a	n/a
13	CTCF	chr3:143106780-143106930	HVMF	connective:	n/a	chr3:143106829-143106842 chr3:143106830-143106840 chr3:143106827-143106845
14	CTCF	chr3:143106620-143106770	HFF-Myc	foreskin:	n/a	n/a
15	CTCF	chr3:143106740-143106890	AoAF	blood vessel:	n/a	chr3:143106829-143106842 chr3:143106830-143106840 chr3:143106827-143106845
16	CTCF	chr3:143106700-143106850	AoAF	blood vessel:	n/a	chr3:143106829-143106842 chr3:143106830-143106840 chr3:143106827-143106845
17	E2F4	chr3:143121213-143121370	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr3:143087214-143087391	MCF10A-Er-Src	breast:	n/a	chr3:143087272-143087281
19	E2F4	chr3:143089994-143090035	MCF10A-Er-Src	breast:	n/a	n/a
20	EBF1	chr3:143133770-143133914	GM12878	blood:	n/a	n/a
21	EBF1	chr3:143108248-143108463	GM12878	blood:	n/a	chr3:143108387-143108397 chr3:143108387-143108396 chr3:143108385-143108396
22	EP300	chr3:143087434-143087666	K562	blood:	n/a	n/a
23	ESR1	chr3:143099313-143099594	ECC-1	luminal epithelium:	n/a	n/a
24	ESR1	chr3:143099270-143099593	ECC-1	luminal epithelium:	n/a	n/a
25	FAM48A	chr3:143116703-143116803	GM12878	blood:	n/a	n/a
26	FOS	chr3:143086072-143086360	MCF10A-Er-Src	breast:	n/a	chr3:143086218-143086226 chr3:143086218-143086226 chr3:143086218-143086225 chr3:143086216-143086228 chr3:143086217-143086227
27	FOS	chr3:143094582-143094715	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr3:143086048-143086374	MCF10A-Er-Src	breast:	n/a	chr3:143086218-143086226 chr3:143086218-143086226 chr3:143086218-143086225 chr3:143086216-143086228 chr3:143086217-143086227
29	FOS	chr3:143094528-143094889	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr3:143094532-143094856	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr3:143094528-143094813	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr3:143100563-143100775	MCF10A-Er-Src	breast:	n/a	n/a
33	FOXA2	chr3:143109583-143109965	A549	lung:	n/a	n/a
34	GATA3	chr3:143086067-143086566	SK-N-SH	brain:	n/a	chr3:143086242-143086263 chr3:143086249-143086256 chr3:143086249-143086256 chr3:143086249-143086256
35	GATA3	chr3:143085943-143086532	SK-N-SH	brain:	n/a	chr3:143086242-143086263 chr3:143086249-143086256 chr3:143086249-143086256 chr3:143086249-143086256
36	GTF2F1	chr3:143127953-143127962	H1-hESC	embryonic stem cell:	n/a	n/a
37	JUN	chr3:143098396-143098397	H1-hESC	embryonic stem cell:	n/a	n/a
38	KAP1	chr3:143121456-143121832	K562	blood:	n/a	n/a
39	KAP1	chr3:143099825-143100390	K562	blood:	n/a	n/a
40	MAFF	chr3:143085543-143086383	K562	blood:	n/a	chr3:143086216-143086234 chr3:143086215-143086229
41	MAFF	chr3:143086104-143086389	HepG2	liver:	n/a	chr3:143086216-143086234 chr3:143086215-143086229
42	MAFK	chr3:143086113-143086335	IMR90	lung:	n/a	chr3:143086216-143086225 chr3:143086218-143086228 chr3:143086212-143086232 chr3:143086214-143086230 chr3:143086215-143086229 chr3:143086219-143086228
43	MAFK	chr3:143086066-143086384	HepG2	liver:	n/a	chr3:143086216-143086225 chr3:143086218-143086228 chr3:143086212-143086232 chr3:143086214-143086230 chr3:143086215-143086229 chr3:143086219-143086228
44	MAX	chr3:143102595-143102789	K562	blood:	n/a	n/a
45	MAX	chr3:143088581-143088861	NB4	blood:	n/a	chr3:143088676-143088686
46	MTA3	chr3:143130657-143131334	GM12878	blood:	n/a	n/a
47	MYC	chr3:143092548-143092671	MCF10A-Er-Src	breast:	n/a	n/a
48	NFIC	chr3:143099285-143099732	ECC-1	luminal epithelium:	n/a	n/a
49	NRF1	chr3:143089894-143089897	K562	blood:	n/a	n/a
50	POLR2A	chr3:143121726-143121844	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:143127934-143127984	HepG2	liver:	n/a
2	chr3:143127934-143127984	MCF-7	breast:	n/a
3	chr3:143127934-143127984	ECC-1	luminal epithelium:	n/a
4	chr3:143097071-143097121	GM12878	blood:	n/a
5	chr3:143097071-143097121	HRPEpiC	eye:	n/a
6	chr3:143127934-143127984	NH-A	brain:	n/a
7	chr3:143127934-143127984	HEEpiC	esophagus:	n/a
8	chr3:143097071-143097121	NB4	blood:	n/a
9	chr3:143097071-143097121	AoSMC	blood vessel:	n/a
10	chr3:143097071-143097121	HL-60	blood:	n/a
11	chr3:143097071-143097121	Hela-S3	cervix:	n/a
12	chr3:143097071-143097121	HCPEpiC	choroid plexus:	n/a
13	chr3:143127934-143127984	LNCaP	prostate:	n/a
14	chr3:143127934-143127984	HCPEpiC	choroid plexus:	n/a
15	chr3:143097071-143097121	GM12892	blood:	n/a
16	chr3:143097071-143097121	RPTEC	kidney:	n/a
17	chr3:143127934-143127984	PFSK-1	brain:	n/a
18	chr3:143127934-143127984	AG09309	skin:	n/a
19	chr3:143127934-143127984	NT2-D1	testis:	n/a
20	chr3:143127934-143127984	T-47D	breast:	n/a
21	chr3:143127934-143127984	HRE	kidney:	n/a
22	chr3:143127934-143127984	HRPEpiC	eye:	n/a
23	chr3:143127934-143127984	HCF	heart:	n/a
24	chr3:143127934-143127984	NHBE	bronchial:	n/a
25	chr3:143127934-143127984	GM19239	blood:	n/a
26	chr3:143127934-143127984	U87	brain:	n/a
27	chr3:143127934-143127984	AG09319	gingival:	n/a
28	chr3:143127934-143127984	SAEC	small airway:	n/a
29	chr3:143097071-143097121	AG04449	skin:	fetal
30	chr3:143127934-143127984	AG04449	skin:	fetal
31	chr3:143097071-143097121	MCF10A-Er-Src	breast:	n/a
32	chr3:143127934-143127984	SK-N-SH	brain:	n/a
33	chr3:143127934-143127984	RPTEC	kidney:	n/a
34	chr3:143097071-143097121	HIPEpiC	eye:	n/a
35	chr3:143097071-143097121	HCF	heart:	n/a
36	chr3:143097071-143097121	Hepatocyte	liver:	n/a
37	chr3:143127934-143127984	MCF10A-Er-Src	breast:	n/a
38	chr3:143097071-143097121	NHDF-neo	bronchial:	n/a
39	chr3:143127934-143127984	HCM	heart:	n/a
40	chr3:143127934-143127984	HNPCEpiC	eye:	n/a
41	chr3:143097071-143097121	A549	lung:	n/a
42	chr3:143127934-143127984	HIPEpiC	eye:	n/a
43	chr3:143097071-143097121	Caco-2	colon:	n/a
44	chr3:143097071-143097121	T-47D	breast:	n/a
45	chr3:143097071-143097121	HMEC	breast:	n/a
46	chr3:143097071-143097121	HEK293	kidney:	embryo
47	chr3:143127934-143127984	H1-hESC	embryonic stem cell:	embryo
48	chr3:143127934-143127984	IMR90	lung:	fetal
49	chr3:143127934-143127984	GM06990	blood:	n/a
50	chr3:143127934-143127984	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:142841457..142843683-chr3:143117287..143118954,2	K562	blood:
2	chr3:143076644..143082089-chr3:143083976..143087336,5	K562	blood:
3	chr3:142702091..142703863-chr3:143124368..143127193,2	K562	blood:
4	chr3:143089798..143091848-chr3:143094330..143096533,2	K562	blood:
5	chr3:143068671..143071346-chr3:143094512..143096094,2	K562	blood:
6	chr3:143107077..143109366-chr3:143114729..143117403,2	K562	blood:
7	chr3:143106712..143109351-chr3:143117570..143120299,2	K562	blood:
8	chr3:143083767..143087407-chr3:143088395..143091311,3	K562	blood:
9	chr3:142835479..142837341-chr3:143085961..143087735,2	K562	blood:
10	chr3:143047507..143050166-chr3:143127472..143129524,2	K562	blood:
11	chr3:143083767..143087407-chr3:143088395..143091311,3	K562	blood:
12	chr3:143094103..143096377-chr3:143119769..143122751,2	K562	blood:
13	chr3:143094103..143096377-chr3:143119769..143122751,2	K562	blood:
14	chr3:143099826..143101455-chr3:143101968..143104391,2	K562	blood:
15	chr3:143106712..143109351-chr3:143117570..143120299,2	K562	blood:
16	chr3:143107077..143109366-chr3:143114729..143117403,2	K562	blood:
17	chr3:143079326..143082089-chr3:143083976..143087226,3	K562	blood:
18	chr3:143089798..143091848-chr3:143094330..143096533,2	K562	blood:
19	chr3:143081768..143084316-chr3:143087882..143089415,2	MCF-7	breast:
20	chr3:143127774..143129299-chr3:143137124..143139731,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHST2-4	chr3:143100786-143101003	ENSG00000244493.1
2	lnc-CHST2-4	chr3:143100180-143100288	ENSG00000244493.1

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

Extended variants
information (count: 1996 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1996 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4839628	chr3:143086325-143086326	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182854452	chr3:143086340-143086341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551156120	chr3:143086355-143086356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569473138	chr3:143086412-143086413	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs536765817	chr3:143086426-143086427	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs557508877	chr3:143086441-143086442	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs555141831	chr3:143086477-143086478	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs567282521	chr3:143086488-143086489	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs534309460	chr3:143086499-143086500	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs187562028	chr3:143086505-143086506	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs578249688	chr3:143086506-143086507	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs545668666	chr3:143086508-143086509	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs557595483	chr3:143086522-143086523	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs575870430	chr3:143086531-143086532	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs13088850	chr3:143086536-143086537	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs13088980	chr3:143086549-143086550	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs13089392	chr3:143086559-143086560	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs13089399	chr3:143086568-143086569	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs543126488	chr3:143086600-143086601	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs370817688	chr3:143086618-143086619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs373295767	chr3:143086679-143086680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528520617	chr3:143086713-143086714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs367614376	chr3:143086747-143086748	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559267617	chr3:143086792-143086793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533067684	chr3:143086853-143086854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149185247	chr3:143086857-143086858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569537119	chr3:143086892-143086893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375306737	chr3:143086926-143086927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1604378	chr3:143086937-143086938	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs1604377	chr3:143086952-143086953	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs376886186	chr3:143087002-143087003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567242357	chr3:143087014-143087015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191839810	chr3:143087050-143087051	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576165569	chr3:143087088-143087089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552698710	chr3:143087103-143087104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs35440270	chr3:143087107-143087108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79532799	chr3:143087122-143087123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570923882	chr3:143087150-143087151	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538098781	chr3:143087158-143087159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539354742	chr3:143087160-143087161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557656734	chr3:143087166-143087167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570187738	chr3:143087204-143087205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539297954	chr3:143087209-143087210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575934920	chr3:143087217-143087218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115882251	chr3:143087236-143087237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529124231	chr3:143087305-143087306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555086741	chr3:143087324-143087325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540932384	chr3:143087331-143087332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112214792	chr3:143087336-143087337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559661575	chr3:143087376-143087377	Enhancers 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
Adrenocortical carcinoma	18281524	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:128 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143068200-143091800	Weak transcription	Lung	lung
2	chr3:143070200-143088600	Weak transcription	Aorta	Aorta
3	chr3:143071600-143102400	Weak transcription	Esophagus	oesophagus
4	chr3:143072000-143099400	Weak transcription	Ovary	ovary
5	chr3:143073400-143089600	Weak transcription	Psoas Muscle	Psoas
6	chr3:143077400-143104800	Weak transcription	Brain Hippocampus Middle	brain
7	chr3:143082200-143086400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr3:143082400-143102200	Weak transcription	Primary B cells from cord blood	blood
9	chr3:143083000-143096600	Weak transcription	Primary T cells from cord blood	blood
10	chr3:143083200-143096000	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr3:143083400-143087200	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr3:143083400-143098000	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr3:143084400-143086600	Enhancers	K562	blood
14	chr3:143084600-143087200	Weak transcription	Dnd41	blood
15	chr3:143085800-143103200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr3:143086200-143087400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr3:143086400-143086600	ZNF genes & repeats	Right Ventricle	heart
18	chr3:143087200-143087800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr3:143087200-143088400	Enhancers	Dnd41	blood
20	chr3:143088400-143096800	Weak transcription	Dnd41	blood
21	chr3:143088600-143088800	ZNF genes & repeats	Aorta	Aorta
22	chr3:143088800-143099800	Weak transcription	Aorta	Aorta
23	chr3:143092000-143092600	Enhancers	Liver	Liver
24	chr3:143094000-143099400	Weak transcription	Spleen	Spleen
25	chr3:143094000-143099600	Weak transcription	Adipose Nuclei	Adipose
26	chr3:143094800-143095000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
27	chr3:143095000-143096600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr3:143096000-143098200	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr3:143096600-143097800	Enhancers	H1 Cell Line	embryonic stem cell
30	chr3:143096600-143097800	Enhancers	Primary T cells from cord blood	blood
31	chr3:143096600-143097800	Enhancers	Fetal Thymus	thymus
32	chr3:143096800-143098600	Enhancers	Dnd41	blood
33	chr3:143097000-143100000	Weak transcription	Gastric	stomach
34	chr3:143097200-143097600	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr3:143097200-143097800	Enhancers	H9 Cell Line	embryonic stem cell
36	chr3:143097200-143097800	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr3:143097200-143097800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr3:143097200-143098000	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr3:143097200-143098200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr3:143097400-143097800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr3:143097600-143101000	Weak transcription	Fetal Lung	lung
42	chr3:143097800-143098200	Weak transcription	Fetal Thymus	thymus
43	chr3:143097800-143100000	Weak transcription	Primary T cells from cord blood	blood
44	chr3:143098000-143098400	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr3:143098200-143098400	Enhancers	Fetal Thymus	thymus
46	chr3:143098400-143099200	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr3:143098400-143101800	Weak transcription	Fetal Thymus	thymus
48	chr3:143098600-143099400	Weak transcription	Dnd41	blood
49	chr3:143099200-143099400	Weak transcription	GM12878-XiMat	blood
50	chr3:143099200-143100600	Strong transcription	Monocytes-CD14+_RO01746	blood

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