Variant report

Variant	nsv967072
Chromosome Location	chr3:138543196-138550847
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	ARID3A	chr3:138542527-138543276	HepG2	liver:	n/a	n/a
2	ATF2	chr3:138542557-138543202	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr3:138542568-138543230	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr3:138550778-138550781	K562	blood:	n/a	n/a
5	CUX1	chr3:138544540-138544589	K562	blood:	n/a	n/a
6	EP300	chr3:138542425-138543205	ECC-1	luminal epithelium:	n/a	chr3:138542747-138542756
7	EP300	chr3:138542604-138543220	K562	blood:	n/a	chr3:138542747-138542756
8	FOXA2	chr3:138542377-138543318	HepG2	liver:	n/a	n/a
9	GATA3	chr3:138542422-138543200	A549	lung:	n/a	n/a
10	HEY1	chr3:138544219-138544537	K562	blood:	n/a	n/a
11	HEY1	chr3:138544671-138544895	K562	blood:	n/a	n/a
12	IRF1	chr3:138542593-138543251	K562	blood:	n/a	n/a
13	JUN	chr3:138542595-138543251	K562	blood:	n/a	chr3:138542747-138542755 chr3:138542747-138542754 chr3:138542747-138542755 chr3:138542745-138542757 chr3:138542746-138542756
14	JUND	chr3:138542464-138543362	SK-N-SH	brain:	n/a	chr3:138542747-138542755 chr3:138542747-138542754 chr3:138542745-138542756 chr3:138542747-138542755 chr3:138542745-138542757 chr3:138542746-138542756
15	JUND	chr3:138542550-138543273	H1-hESC	embryonic stem cell:	n/a	chr3:138542747-138542755 chr3:138542747-138542754 chr3:138542745-138542756 chr3:138542747-138542755 chr3:138542745-138542757 chr3:138542746-138542756
16	MAFK	chr3:138547992-138548303	HepG2	liver:	n/a	chr3:138548125-138548136
17	MAFK	chr3:138542571-138543199	H1-hESC	embryonic stem cell:	n/a	chr3:138543095-138543106 chr3:138542747-138542757 chr3:138542748-138542757 chr3:138542746-138542761
18	MAFK	chr3:138548056-138548295	IMR90	lung:	n/a	chr3:138548125-138548136
19	MEF2A	chr3:138548642-138548970	GM12878	blood:	n/a	n/a
20	POLR2A	chr3:138544334-138544535	K562	blood:	n/a	n/a
21	POLR2A	chr3:138544890-138544914	K562	blood:	n/a	n/a
22	POLR2A	chr3:138544270-138544414	GM12878	blood:	n/a	n/a
23	POLR2A	chr3:138544179-138544492	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr3:138544703-138544830	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr3:138542578-138543196	PANC-1	pancreas:	n/a	n/a
26	POLR2A	chr3:138544621-138544977	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr3:138549158-138549336	HepG2	liver:	n/a	n/a
28	POLR2A	chr3:138544141-138544508	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr3:138544516-138544530	MCF-7	breast:	n/a	n/a
30	POLR2A	chr3:138544628-138544923	GM12878	blood:	n/a	n/a
31	POLR2A	chr3:138544116-138544955	GM12878	blood:	n/a	n/a
32	POLR2A	chr3:138549424-138549431	K562	blood:	n/a	n/a
33	POLR2A	chr3:138544236-138544473	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr3:138544663-138544815	GM12878	blood:	n/a	n/a
35	POLR2A	chr3:138549288-138549343	MCF-7	breast:	n/a	n/a
36	POLR2A	chr3:138544538-138544586	MCF-7	breast:	n/a	n/a
37	POLR2A	chr3:138545621-138545783	HepG2	liver:	n/a	n/a
38	POLR2A	chr3:138550642-138554801	K562	blood:	n/a	n/a
39	POLR2A	chr3:138547438-138547492	K562	blood:	n/a	n/a
40	POLR2A	chr3:138550836-138550916	K562	blood:	n/a	n/a
41	POLR2A	chr3:138546015-138546341	K562	blood:	n/a	n/a
42	POLR2A	chr3:138544540-138544815	K562	blood:	n/a	n/a
43	POLR2A	chr3:138550636-138550743	HepG2	liver:	n/a	n/a
44	POLR2A	chr3:138543821-138544103	GM12878	blood:	n/a	n/a
45	POLR2A	chr3:138543650-138543684	K562	blood:	n/a	n/a
46	POLR2A	chr3:138543766-138544545	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr3:138544172-138544516	GM12878	blood:	n/a	n/a
48	POLR2A	chr3:138543755-138543859	K562	blood:	n/a	n/a
49	POLR2A	chr3:138542619-138545078	K562	blood:	n/a	n/a
50	POLR2A	chr3:138543822-138544724	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:138544244..138546193-chr3:138552425..138554988,2	MCF-7	breast:
2	chr3:138532061..138535019-chr3:138545611..138549640,3	K562	blood:
3	chr3:138542924..138545865-chr3:138546494..138548470,2	MCF-7	breast:
4	chr3:138525639..138527361-chr3:138540690..138543312,2	K562	blood:
5	chr3:138541276..138545209-chr3:138550830..138554565,5	MCF-7	breast:
6	chr3:138548916..138550963-chr3:138596429..138598640,2	K562	blood:
7	chr3:138535838..138538762-chr3:138546948..138549872,2	K562	blood:
8	chr3:138541873..138544767-chr3:138546803..138549506,3	K562	blood:
9	chr3:138541276..138545209-chr3:138550830..138554565,5	MCF-7	breast:
10	chr3:138547576..138550266-chr3:138633999..138636358,2	MCF-7	breast:
11	chr3:138546890..138548740-chr3:138633095..138635924,3	K562	blood:
12	chr3:138521559..138523746-chr3:138548742..138551638,2	K562	blood:
13	chr3:138539146..138542013-chr3:138544348..138547069,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C3orf72-4	chr3:138544861-138545200	NONHSAT092342
2	lnc-C3orf72-4	chr3:138543905-138545171	NONHSAT092341
3	lnc-C3orf72-4	chr3:138544653-138544666	NONHSAT092342
4	lnc-C3orf72-4	chr3:138544770-138544844	NONHSAT092342

Variant related genes	Relation type
EEF1A1P25	TF binding region
ENSG00000051382	chromatin interactions
ENSG00000241429	chromatin interactions

Extended variants
information (count: 291 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530136397	chr3:138543206-138543207	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs553415827	chr3:138543219-138543220	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs543835503	chr3:138543229-138543230	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs563813987	chr3:138543232-138543233	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs532612303	chr3:138543251-138543252	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs566840406	chr3:138543294-138543295	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs185111367	chr3:138543358-138543359	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs149218393	chr3:138543362-138543363	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs565854207	chr3:138543365-138543366	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs78430630	chr3:138543425-138543426	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs374663596	chr3:138543442-138543443	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs548496905	chr3:138543486-138543487	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs568240677	chr3:138543491-138543492	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs12631799	chr3:138543508-138543509	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs568559744	chr3:138543564-138543565	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs537094772	chr3:138543575-138543576	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs550149822	chr3:138543579-138543580	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs570220859	chr3:138543584-138543585	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs189993019	chr3:138543620-138543621	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs112460785	chr3:138543628-138543629	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs55751451	chr3:138543638-138543639	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs58172526	chr3:138543672-138543673	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs138954336	chr3:138543674-138543675	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs534884683	chr3:138543677-138543678	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs555291450	chr3:138543687-138543688	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs575024604	chr3:138543688-138543689	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs544388432	chr3:138543706-138543707	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs182264100	chr3:138543717-138543718	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs71312596	chr3:138543732-138543733	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs368995036	chr3:138543735-138543736	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs563629784	chr3:138543741-138543742	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs57342129	chr3:138543756-138543757	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs113118656	chr3:138543799-138543800	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs375627965	chr3:138543825-138543826	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs112240647	chr3:138543866-138543867	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs189456062	chr3:138543894-138543895	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs55718096	chr3:138543962-138543963	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs142061603	chr3:138544005-138544006	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs145672137	chr3:138544025-138544026	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs143023518	chr3:138544034-138544035	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs577877746	chr3:138544077-138544078	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs180762452	chr3:138544147-138544148	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs138220184	chr3:138544186-138544187	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs141814448	chr3:138544200-138544201	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs539162554	chr3:138544213-138544214	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs546316912	chr3:138544225-138544226	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs566441954	chr3:138544262-138544263	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs559737571	chr3:138544269-138544270	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs554825078	chr3:138544270-138544271	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs575082460	chr3:138544305-138544306	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Cancer	21129771	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
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	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
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	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
Developmental delay	21147756	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD

Chromatin state (count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:138504000-138552000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:138506000-138551800	Weak transcription	Primary B cells from cord blood	blood
3	chr3:138513400-138544400	Weak transcription	Fetal Muscle Leg	muscle
4	chr3:138528800-138552600	Weak transcription	Colonic Mucosa	Colon
5	chr3:138529400-138544400	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr3:138535000-138543200	Weak transcription	Thymus	Thymus
7	chr3:138535000-138544000	Weak transcription	Fetal Thymus	thymus
8	chr3:138535000-138544200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr3:138535200-138543600	Weak transcription	Dnd41	blood
10	chr3:138535200-138543800	Weak transcription	Primary T cells from cord blood	blood
11	chr3:138535200-138551600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr3:138537000-138552200	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr3:138537200-138544200	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr3:138537200-138544200	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr3:138537200-138548400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr3:138537200-138552000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr3:138537200-138552200	Weak transcription	Colon Smooth Muscle	Colon
18	chr3:138537400-138544000	Weak transcription	Primary hematopoietic stem cells	blood
19	chr3:138537400-138544400	Weak transcription	Spleen	Spleen
20	chr3:138537400-138551400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr3:138537400-138552200	Weak transcription	Brain Anterior Caudate	brain
22	chr3:138537600-138543800	Weak transcription	Gastric	stomach
23	chr3:138537600-138543800	Weak transcription	GM12878-XiMat	blood
24	chr3:138537600-138544000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr3:138537600-138544000	Weak transcription	Liver	Liver
26	chr3:138537600-138544200	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr3:138537600-138544200	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr3:138537600-138544200	Weak transcription	Duodenum Mucosa	Duodenum
29	chr3:138537600-138544400	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr3:138537600-138544400	Weak transcription	Stomach Smooth Muscle	stomach
31	chr3:138537600-138549000	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr3:138537600-138551200	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr3:138537600-138551400	Weak transcription	Primary B cells from peripheral blood	blood
34	chr3:138537600-138551400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr3:138537600-138552000	Weak transcription	Brain Hippocampus Middle	brain
36	chr3:138537600-138552200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr3:138537600-138552200	Weak transcription	Brain Substantia Nigra	brain
38	chr3:138537600-138552400	Weak transcription	Brain Angular Gyrus	brain
39	chr3:138537600-138552400	Weak transcription	Brain Cingulate Gyrus	brain
40	chr3:138537600-138552600	Weak transcription	Ovary	ovary
41	chr3:138538000-138544000	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr3:138538000-138544400	Weak transcription	Psoas Muscle	Psoas
43	chr3:138538200-138544200	Weak transcription	Right Atrium	heart
44	chr3:138538200-138544400	Weak transcription	Lung	lung
45	chr3:138538400-138544000	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr3:138539200-138543400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr3:138539200-138551200	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr3:138539200-138552200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr3:138539400-138544600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr3:138539400-138544600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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