Variant report

Variant	nsv591398
Chromosome Location	chr3:121046468-121154193
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:287)
CpG islands
(count:183)
Chromatin interactive
region (count:20)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:121150837-121151409	GM12878	blood:	n/a	n/a
2	ATF2	chr3:121150918-121151361	GM12878	blood:	n/a	n/a
3	BATF	chr3:121151014-121151263	GM12878	blood:	n/a	n/a
4	BCLAF1	chr3:121150752-121151398	GM12878	blood:	n/a	n/a
5	CCNT2	chr3:121132208-121132533	K562	blood:	n/a	n/a
6	CEBPB	chr3:121136957-121137462	A549	lung:	n/a	n/a
7	CEBPB	chr3:121137051-121137400	A549	lung:	n/a	n/a
8	CEBPB	chr3:121137029-121137429	A549	lung:	n/a	n/a
9	CEBPB	chr3:121133855-121133981	K562	blood:	n/a	n/a
10	CEBPB	chr3:121133819-121134072	IMR90	lung:	n/a	n/a
11	CEBPB	chr3:121137054-121137409	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr3:121137032-121137414	HepG2	liver:	n/a	n/a
13	CEBPB	chr3:121137097-121137339	HepG2	liver:	n/a	n/a
14	CEBPB	chr3:121137122-121137304	HepG2	liver:	n/a	n/a
15	CEBPB	chr3:121137025-121137334	MCF-7	breast:	n/a	n/a
16	CEBPB	chr3:121137053-121137413	IMR90	lung:	n/a	n/a
17	CEBPB	chr3:121137052-121137334	K562	blood:	n/a	n/a
18	CEBPB	chr3:121137038-121137374	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr3:121137032-121137414	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr3:121137031-121137348	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr3:121137090-121137411	MCF-7	breast:	n/a	n/a
22	CEBPB	chr3:121133848-121133998	A549	lung:	n/a	n/a
23	CEBPB	chr3:121137039-121137410	K562	blood:	n/a	n/a
24	CTCF	chr3:121048013-121048318	MCF-7	breast:	n/a	chr3:121048109-121048130
25	CTCF	chr3:121048080-121048230	HMF	breast:	n/a	chr3:121048109-121048130
26	CTCF	chr3:121150660-121150810	HCFaa	heart:	n/a	n/a
27	CTCF	chr3:121130880-121131030	HMF	breast:	n/a	chr3:121130967-121130985 chr3:121130962-121130983
28	CTCF	chr3:121107402-121107519	GM13976	blood:	n/a	n/a
29	CTCF	chr3:121072703-121072722	Pancreas_OC	pancreas:	n/a	n/a
30	CTCF	chr3:121048114-121048129	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr3:121048020-121048170	MCF-7	breast:	n/a	chr3:121048109-121048130
32	CTCF	chr3:121114673-121114696	Medullo	brain:	n/a	n/a
33	CTCF	chr3:121048028-121048210	MCF-7	breast:	n/a	chr3:121048109-121048130
34	CTCF	chr3:121150680-121150830	HMF	breast:	n/a	n/a
35	CTCF	chr3:121150660-121150810	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr3:121150640-121150790	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr3:121150820-121150970	NHLF	lung:	n/a	n/a
38	CTCF	chr3:121081220-121081370	GM12871	blood:	n/a	n/a
39	CTCF	chr3:121150660-121150810	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr3:121151154-121151185	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr3:121152700-121152850	GM12867	blood:	n/a	n/a
42	CTCF	chr3:121118780-121118930	GM12869	blood:	n/a	n/a
43	CTCF	chr3:121150580-121150730	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr3:121072654-121072758	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr3:121048077-121048187	MCF-7	breast:	n/a	chr3:121048109-121048130
46	CTCF	chr3:121130950-121131007	MCF-7	breast:	n/a	chr3:121130967-121130985 chr3:121130962-121130983
47	CTCF	chr3:121047960-121048110	MCF-7	breast:	n/a	n/a
48	CTCF	chr3:121048060-121048210	RPTEC	kidney:	n/a	chr3:121048109-121048130
49	CTCF	chr3:121092691-121092774	ProgFib	skin:	n/a	n/a
50	CTCF	chr3:121150680-121150830	HCPEpiC	choroid plexus:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:121142525-121142575	HepG2	liver:	n/a
2	chr3:121142525-121142575	HCPEpiC	choroid plexus:	n/a
3	chr3:121142525-121142575	HRCEpiC	kidney:	n/a
4	chr3:121142525-121142575	HMEC	breast:	n/a
5	chr3:121142525-121142575	T-47D	breast:	n/a
6	chr3:121151186-121151236	T-47D	breast:	n/a
7	chr3:121150715-121150765	PrEC	prostate:	n/a
8	chr3:121142525-121142575	GM12878	blood:	n/a
9	chr3:121142525-121142575	GM19239	blood:	n/a
10	chr3:121142525-121142575	CMK	blood:	n/a
11	chr3:121142525-121142575	SK-N-SH_RA	brain:	n/a
12	chr3:121150715-121150765	AG09309	skin:	n/a
13	chr3:121150715-121150765	HRPEpiC	eye:	n/a
14	chr3:121151186-121151236	H1-hESC	embryonic stem cell:	embryo
15	chr3:121150715-121150765	Hepatocyte	liver:	n/a
16	chr3:121151186-121151236	BJ	skin:	n/a
17	chr3:121142525-121142575	AG09309	skin:	n/a
18	chr3:121150715-121150765	GM06990	blood:	n/a
19	chr3:121150715-121150765	NB4	blood:	n/a
20	chr3:121151186-121151236	HCT-116	colon:	n/a
21	chr3:121151186-121151236	HCF	heart:	n/a
22	chr3:121142525-121142575	GM12891	blood:	n/a
23	chr3:121151186-121151236	SKMC	muscle:	n/a
24	chr3:121151186-121151236	NHBE	bronchial:	n/a
25	chr3:121150715-121150765	NT2-D1	testis:	n/a
26	chr3:121151186-121151236	HAEpiC	amniotic membrane:	n/a
27	chr3:121150715-121150765	BE2_C	brain:	n/a
28	chr3:121142525-121142575	RPTEC	kidney:	n/a
29	chr3:121150715-121150765	AoSMC	blood vessel:	n/a
30	chr3:121151186-121151236	GM12891	blood:	n/a
31	chr3:121150715-121150765	SK-N-SH	brain:	n/a
32	chr3:121151186-121151236	HRPEpiC	eye:	n/a
33	chr3:121142525-121142575	HCT-116	colon:	n/a
34	chr3:121150715-121150765	AG09319	gingival:	n/a
35	chr3:121150715-121150765	HNPCEpiC	eye:	n/a
36	chr3:121142525-121142575	NHDF-neo	bronchial:	n/a
37	chr3:121150715-121150765	SKMC	muscle:	n/a
38	chr3:121150715-121150765	HEK293	kidney:	embryo
39	chr3:121151186-121151236	U87	brain:	n/a
40	chr3:121150715-121150765	U87	brain:	n/a
41	chr3:121142525-121142575	ECC-1	luminal epithelium:	n/a
42	chr3:121151186-121151236	Caco-2	colon:	n/a
43	chr3:121142525-121142575	ovcar-3	ovarian:	n/a
44	chr3:121151186-121151236	HNPCEpiC	eye:	n/a
45	chr3:121150715-121150765	HL-60	blood:	n/a
46	chr3:121142525-121142575	SKMC	muscle:	n/a
47	chr3:121150715-121150765	NH-A	brain:	n/a
48	chr3:121150715-121150765	Jurkat	blood:	n/a
49	chr3:121142525-121142575	SK-N-SH	brain:	n/a
50	chr3:121150715-121150765	MCF10A-Er-Src	breast:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:121047561..121048621-chr3:121247919..121248785,3	MCF-7	breast:
2	chr3:121134688..121138349-chr3:121139086..121141700,5	K562	blood:
3	chr3:121143314..121145833-chr3:121149976..121152815,2	MCF-7	breast:
4	chr20:17868453..17869206-chr3:121103732..121104423,2	MCF-7	breast:
5	chr3:121129952..121132930-chr3:121134868..121138546,3	K562	blood:
6	chr3:121121830..121124199-chr3:121125934..121129748,5	K562	blood:
7	chr3:121150437..121151324-chr3:121212003..121212905,2	MCF-7	breast:
8	chr3:121125400..121127225-chr3:121128769..121131952,3	K562	blood:
9	chr3:121125400..121127225-chr3:121128769..121131952,3	K562	blood:
10	chr3:121152541..121155166-chr3:121158856..121160501,2	K562	blood:
11	chr3:121121830..121124199-chr3:121125934..121129748,5	K562	blood:
12	chr3:121138259..121140292-chr3:121185745..121188174,2	K562	blood:
13	chr3:121135285..121138210-chr3:121139443..121141521,3	K562	blood:
14	chr3:121122561..121125182-chr3:121127949..121129748,3	K562	blood:
15	chr3:121122561..121125182-chr3:121127949..121129748,3	K562	blood:
16	chr3:121134688..121138349-chr3:121139086..121141700,5	K562	blood:
17	chr3:121143314..121145833-chr3:121149976..121152815,2	MCF-7	breast:
18	chr3:121135285..121138210-chr3:121139443..121141521,3	K562	blood:
19	chr3:121152758..121154352-chr3:121155971..121158501,2	MCF-7	breast:
20	chr3:121129952..121132930-chr3:121134868..121138546,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARGFX-1	chr3:121075838-121076787	NONHSAT091471

No data

Variant related genes	Relation type
ENSG00000242103	TF binding region
ENSG00000242103	CpG island
ENSG00000233625	chromatin interactions

Extended variants
information (count: 2757 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2757 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1355452	chr3:121046468-121046469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs545891495	chr3:121046470-121046471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556329425	chr3:121046471-121046472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190480746	chr3:121046546-121046547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs193102950	chr3:121046595-121046596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112002154	chr3:121046631-121046632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535974653	chr3:121046652-121046653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555924413	chr3:121046654-121046655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185885930	chr3:121046668-121046669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs61796934	chr3:121046670-121046671	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs6793427	chr3:121046673-121046674	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs189948719	chr3:121046798-121046799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181652908	chr3:121046849-121046850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538277203	chr3:121046880-121046881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562194111	chr3:121046890-121046891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185383514	chr3:121046987-121046988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188636035	chr3:121046993-121046994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112503938	chr3:121047004-121047005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561486023	chr3:121047029-121047030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371876775	chr3:121047092-121047093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532273167	chr3:121047100-121047101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142019540	chr3:121047134-121047135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185964277	chr3:121047164-121047165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs58491112	chr3:121047183-121047184	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs533273192	chr3:121047185-121047186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs367597997	chr3:121047313-121047314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549778676	chr3:121047317-121047318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569943610	chr3:121047318-121047319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376209600	chr3:121047320-121047321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191213051	chr3:121047361-121047362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565694017	chr3:121047393-121047394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571522015	chr3:121047405-121047406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567547552	chr3:121047425-121047426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536498944	chr3:121047453-121047454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183827142	chr3:121047454-121047455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558143107	chr3:121047469-121047470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577927593	chr3:121047550-121047551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376420252	chr3:121047558-121047559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544120273	chr3:121047567-121047568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372371703	chr3:121047581-121047582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187598014	chr3:121047626-121047627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191485404	chr3:121047632-121047633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183103568	chr3:121047637-121047638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559471864	chr3:121047662-121047663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548467742	chr3:121047694-121047695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs77707938	chr3:121047717-121047718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540731657	chr3:121047737-121047738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564130331	chr3:121047746-121047747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532817450	chr3:121047779-121047780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187035919	chr3:121047852-121047853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	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
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	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
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	22241247	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	17953491	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:371 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:121033600-121052200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr3:121043200-121049000	Weak transcription	Ovary	ovary
3	chr3:121048400-121049400	Enhancers	Fetal Heart	heart
4	chr3:121049000-121050000	Strong transcription	Ovary	ovary
5	chr3:121049000-121050000	Enhancers	HSMMtube	muscle
6	chr3:121049400-121049600	Flanking Active TSS	Fetal Heart	heart
7	chr3:121049600-121049800	Enhancers	Fetal Heart	heart
8	chr3:121049600-121050000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
9	chr3:121049800-121050000	Flanking Active TSS	Fetal Heart	heart
10	chr3:121050000-121050600	Enhancers	Fetal Heart	heart
11	chr3:121050000-121051600	Weak transcription	Ovary	ovary
12	chr3:121051600-121052000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr3:121075800-121076200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
14	chr3:121081200-121081800	Enhancers	Hela-S3	cervix
15	chr3:121087600-121087800	Weak transcription	Ovary	ovary
16	chr3:121087600-121087800	Bivalent/Poised TSS	Right Atrium	heart
17	chr3:121087800-121088000	ZNF genes & repeats	Ovary	ovary
18	chr3:121088000-121092200	Weak transcription	Ovary	ovary
19	chr3:121088200-121099000	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr3:121089400-121091600	Weak transcription	Brain Cingulate Gyrus	brain
21	chr3:121090200-121090800	ZNF genes & repeats	Brain Hippocampus Middle	brain
22	chr3:121090200-121090800	ZNF genes & repeats	Pancreas	Pancrea
23	chr3:121090200-121091000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr3:121090800-121094200	Weak transcription	Brain Hippocampus Middle	brain
25	chr3:121091400-121092800	Weak transcription	Brain Anterior Caudate	brain
26	chr3:121092200-121093000	Strong transcription	Ovary	ovary
27	chr3:121092600-121093000	ZNF genes & repeats	Gastric	stomach
28	chr3:121093000-121117000	Weak transcription	Ovary	ovary
29	chr3:121099200-121099400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr3:121099400-121099800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr3:121099400-121102800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr3:121099800-121101800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr3:121102800-121103000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr3:121116800-121118000	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr3:121117000-121117400	Enhancers	Ovary	ovary
36	chr3:121117000-121117400	Enhancers	HUVEC	blood vessel
37	chr3:121117200-121117600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr3:121117400-121139400	Weak transcription	Ovary	ovary
39	chr3:121129000-121129200	Enhancers	GM12878-XiMat	blood
40	chr3:121129200-121148800	Weak transcription	GM12878-XiMat	blood
41	chr3:121130400-121130800	Enhancers	Muscle Satellite Cultured Cells	--
42	chr3:121130400-121130800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr3:121130400-121130800	Enhancers	HUVEC	blood vessel
44	chr3:121134200-121152600	Weak transcription	Hela-S3	cervix
45	chr3:121134400-121134600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr3:121134600-121146400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr3:121135400-121141200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr3:121135800-121139600	Weak transcription	Brain Germinal Matrix	brain
49	chr3:121135800-121148600	Weak transcription	Thymus	Thymus
50	chr3:121135800-121149000	Weak transcription	A549	lung

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