Variant report

Variant	nsv589843
Chromosome Location	chr3:17412690-17525505
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1096)
CpG islands
(count:0)
Chromatin interactive
region (count:70)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1096 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:17454500-17454738	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:17462080-17462754	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:17506407-17506512	K562	blood:	n/a	n/a
4	ARID3A	chr3:17484122-17484922	K562	blood:	n/a	n/a
5	ARID3A	chr3:17414297-17414619	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:17486399-17486776	K562	blood:	n/a	n/a
7	ARID3A	chr3:17472416-17472770	K562	blood:	n/a	n/a
8	ATF1	chr3:17486434-17486698	K562	blood:	n/a	n/a
9	ATF1	chr3:17520229-17520516	K562	blood:	n/a	n/a
10	ATF1	chr3:17472550-17472822	K562	blood:	n/a	n/a
11	ATF1	chr3:17484669-17484932	K562	blood:	n/a	n/a
12	ATF1	chr3:17484018-17484387	K562	blood:	n/a	n/a
13	ATF2	chr3:17440529-17441152	GM12878	blood:	n/a	n/a
14	ATF2	chr3:17440604-17441083	GM12878	blood:	n/a	n/a
15	ATF3	chr3:17484214-17484440	K562	blood:	n/a	n/a
16	ATF3	chr3:17520011-17520619	A549	lung:	n/a	n/a
17	ATF3	chr3:17486331-17486754	K562	blood:	n/a	n/a
18	ATF3	chr3:17484191-17484365	K562	blood:	n/a	n/a
19	ATF3	chr3:17520058-17520526	A549	lung:	n/a	n/a
20	BACH1	chr3:17473755-17474077	H1-hESC	embryonic stem cell:	n/a	chr3:17473906-17473920
21	BACH1	chr3:17474299-17474445	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr3:17473751-17474065	K562	blood:	n/a	chr3:17473906-17473920
23	BATF	chr3:17440584-17441027	GM12878	blood:	n/a	n/a
24	BATF	chr3:17440687-17441050	GM12878	blood:	n/a	n/a
25	BCL11A	chr3:17440636-17441099	GM12878	blood:	n/a	chr3:17440792-17440801
26	BCL11A	chr3:17440655-17441034	GM12878	blood:	n/a	chr3:17440792-17440801
27	BCL3	chr3:17520027-17520714	A549	lung:	n/a	n/a
28	BCLAF1	chr3:17440619-17441234	GM12878	blood:	n/a	chr3:17440792-17440801
29	BCLAF1	chr3:17440538-17441322	GM12878	blood:	n/a	chr3:17440792-17440801
30	BHLHE40	chr3:17462223-17462521	HepG2	liver:	n/a	n/a
31	BHLHE40	chr3:17428087-17428202	K562	blood:	n/a	n/a
32	BHLHE40	chr3:17462222-17462436	K562	blood:	n/a	n/a
33	BHLHE40	chr3:17484668-17485011	K562	blood:	n/a	n/a
34	BHLHE40	chr3:17520199-17520344	HepG2	liver:	n/a	n/a
35	BHLHE40	chr3:17440644-17441042	GM12878	blood:	n/a	n/a
36	BRCA1	chr3:17454624-17454755	HepG2	liver:	n/a	n/a
37	BRCA1	chr3:17519940-17520632	Hela-S3	cervix:	n/a	n/a
38	CBX3	chr3:17484569-17485167	K562	blood:	n/a	n/a
39	CBX3	chr3:17484048-17484463	K562	blood:	n/a	n/a
40	CCNT2	chr3:17472494-17472658	K562	blood:	n/a	n/a
41	CEBPB	chr3:17414249-17415071	Hela-S3	cervix:	n/a	chr3:17414916-17414927 chr3:17414298-17414309
42	CEBPB	chr3:17414275-17415060	IMR90	lung:	n/a	chr3:17414916-17414927 chr3:17414298-17414309
43	CEBPB	chr3:17517015-17517321	A549	lung:	n/a	n/a
44	CEBPB	chr3:17514883-17514974	A549	lung:	n/a	chr3:17514942-17514953
45	CEBPB	chr3:17470084-17470101	A549	lung:	n/a	n/a
46	CEBPB	chr3:17414823-17415085	A549	lung:	n/a	chr3:17414916-17414927
47	CEBPB	chr3:17475286-17475428	A549	lung:	n/a	n/a
48	CEBPB	chr3:17426381-17426797	A549	lung:	n/a	chr3:17426557-17426568 chr3:17426594-17426605 chr3:17426573-17426584
49	CEBPB	chr3:17486293-17486646	IMR90	lung:	n/a	n/a
50	CEBPB	chr3:17520038-17520681	A549	lung:	n/a	n/a

No data

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:17497865..17499392-chr3:17503466..17506313,2	K562	blood:
2	chr3:17348706..17349625-chr3:17454224..17455498,4	K562	blood:
3	chr3:17497521..17499126-chr3:17503539..17506247,2	MCF-7	breast:
4	chr3:17426084..17429101-chr3:17432439..17434660,3	MCF-7	breast:
5	chr3:17472273..17475803-chr3:17482384..17484152,3	K562	blood:
6	chr3:17520321..17522399-chr3:17522640..17525341,2	K562	blood:
7	chr3:17455901..17458583-chr3:17462176..17465120,2	K562	blood:
8	chr3:17352641..17354178-chr3:17468928..17471565,2	MCF-7	breast:
9	chr3:17485709..17487231-chr3:17783472..17786007,2	MCF-7	breast:
10	chr3:17419146..17421913-chr3:17422228..17424571,2	K562	blood:
11	chr3:17460223..17462241-chr3:17894481..17896425,2	K562	blood:
12	chr3:17348477..17349876-chr3:17454198..17455145,8	MCF-7	breast:
13	chr3:17472087..17473109-chr3:17882519..17883281,4	MCF-7	breast:
14	chr3:17472682..17474282-chr3:17477579..17479223,2	K562	blood:
15	chr3:17472139..17473280-chr3:17881966..17883098,4	MCF-7	breast:
16	chr3:17422120..17423958-chr3:17425722..17427286,2	MCF-7	breast:
17	chr3:17447638..17450232-chr3:17453263..17456160,3	K562	blood:
18	chr3:17459732..17461276-chr3:17463158..17466015,2	MCF-7	breast:
19	chr3:17463498..17465841-chr3:17880192..17882882,2	MCF-7	breast:
20	chr3:17507187..17509434-chr3:17516355..17517975,2	MCF-7	breast:
21	chr3:17472326..17472977-chr3:17727996..17728715,2	MCF-7	breast:
22	chr3:17300011..17301671-chr3:17454009..17455084,9	MCF-7	breast:
23	chr3:17415575..17418642-chr3:17419331..17422264,3	MCF-7	breast:
24	chr3:17484535..17486940-chr3:17491207..17493318,2	MCF-7	breast:
25	chr3:17468044..17471008-chr3:17472912..17474863,2	MCF-7	breast:
26	chr3:17426084..17429101-chr3:17432439..17434660,3	MCF-7	breast:
27	chr3:17497865..17499392-chr3:17503466..17506313,2	K562	blood:
28	chr3:17463709..17467146-chr3:17467192..17469844,3	K562	blood:
29	chr3:17454330..17455065-chr3:17882486..17883391,2	K562	blood:
30	chr3:17472375..17473059-chr3:17727721..17728808,3	MCF-7	breast:
31	chr3:17459732..17461276-chr3:17463158..17466015,2	MCF-7	breast:
32	chr3:17514624..17515516-chr3:17727784..17728694,2	MCF-7	breast:
33	chr3:17472374..17472992-chr3:18020408..18021268,3	MCF-7	breast:
34	chr3:17322980..17323870-chr3:17472180..17472688,2	K562	blood:
35	chr3:17444789..17447315-chr3:17447509..17449518,2	K562	blood:
36	chr3:17415575..17418642-chr3:17419331..17422264,3	MCF-7	breast:
37	chr3:17299624..17302842-chr3:17453304..17456180,3	MCF-7	breast:
38	chr3:17484813..17486609-chr3:17782332..17783917,2	MCF-7	breast:
39	chr3:17497521..17499126-chr3:17503539..17506247,2	MCF-7	breast:
40	chr3:17464487..17468576-chr3:17470106..17473767,3	K562	blood:
41	chr3:17468044..17471008-chr3:17472912..17474863,2	MCF-7	breast:
42	chr3:17454364..17456492-chr3:17782379..17784281,3	MCF-7	breast:
43	chr3:17518313..17520629-chr3:17521648..17524012,2	MCF-7	breast:
44	chr3:17464487..17468576-chr3:17470106..17473767,3	K562	blood:
45	chr3:17510239..17513029-chr3:190165164..190166664,2	MCF-7	breast:
46	chr3:17515336..17515883-chr3:17728199..17729050,2	MCF-7	breast:
47	chr3:17463709..17467146-chr3:17467192..17469844,3	K562	blood:
48	chr3:17348679..17349303-chr3:17454556..17455118,3	MCF-7	breast:
49	chr3:17520321..17522399-chr3:17522640..17525341,2	K562	blood:
50	chr3:17300330..17301004-chr3:17455425..17455933,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLCL2-8	chr3:17506642-17507002	NONHSAT088548
2	lnc-DAZL-5	chr3:17413567-17413626	NONHSAT088543

No data

Variant related genes	Relation type
ENSG00000227309	TF binding region
TBC1D5	TF binding region
ENSG00000131374	chromatin interactions

Extended variants
information (count: 4057 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:4057 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9868647	chr3:17412690-17412691	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs142600593	chr3:17412714-17412715	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566652069	chr3:17412720-17412721	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs527300527	chr3:17412724-17412725	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73156310	chr3:17412725-17412726	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs535843147	chr3:17412732-17412733	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73156313	chr3:17412773-17412774	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs181308255	chr3:17412778-17412779	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185443220	chr3:17412818-17412819	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538979650	chr3:17412848-17412849	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs555693262	chr3:17412858-17412859	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs554851560	chr3:17412911-17412912	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs77688720	chr3:17412923-17412924	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs79519650	chr3:17412927-17412928	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573344655	chr3:17412934-17412935	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562186702	chr3:17412999-17413000	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs150987298	chr3:17413000-17413001	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs374286723	chr3:17413001-17413002	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140767531	chr3:17413058-17413059	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150120825	chr3:17413070-17413071	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553948494	chr3:17413085-17413086	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs115273735	chr3:17413114-17413115	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565160167	chr3:17413139-17413140	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536474004	chr3:17413191-17413192	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561265037	chr3:17413229-17413230	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530159383	chr3:17413241-17413242	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536308826	chr3:17413244-17413245	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs374375474	chr3:17413300-17413301	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs112727545	chr3:17413356-17413357	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs201284450	chr3:17413374-17413375	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560389005	chr3:17413377-17413378	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532303958	chr3:17413396-17413397	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138380076	chr3:17413399-17413400	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs114426519	chr3:17413402-17413403	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs140256342	chr3:17413415-17413416	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs548124090	chr3:17413444-17413445	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs73156314	chr3:17413462-17413463	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs190978502	chr3:17413468-17413469	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs553782595	chr3:17413493-17413494	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs374684563	chr3:17413511-17413512	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs111455911	chr3:17413531-17413532	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs35196536	chr3:17413532-17413533	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs112189940	chr3:17413547-17413548	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs60259858	chr3:17413550-17413551	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs201769045	chr3:17413575-17413576	Strong transcription Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
46	rs113836346	chr3:17413618-17413619	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs373688612	chr3:17413626-17413627	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs377592062	chr3:17413640-17413641	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs149996834	chr3:17413666-17413667	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376409138	chr3:17413682-17413683	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	21364760	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:988 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:17339400-17442200	Weak transcription	Fetal Intestine Small	intestine
2	chr3:17344400-17439000	Weak transcription	Aorta	Aorta
3	chr3:17356200-17412800	Weak transcription	Left Ventricle	heart
4	chr3:17365600-17413000	Weak transcription	Primary hematopoietic stem cells	blood
5	chr3:17379800-17414400	Weak transcription	HSMM	muscle
6	chr3:17398400-17414600	Weak transcription	NHDF-Ad	bronchial
7	chr3:17398600-17414200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr3:17398800-17413000	Weak transcription	Ovary	ovary
9	chr3:17398800-17414600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr3:17398800-17430200	Weak transcription	Pancreas	Pancrea
11	chr3:17398800-17447000	Weak transcription	Fetal Stomach	stomach
12	chr3:17399200-17413000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr3:17401600-17432600	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr3:17402400-17443200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr3:17402600-17412800	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr3:17402600-17451000	Weak transcription	Gastric	stomach
17	chr3:17403000-17443000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr3:17403200-17413600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr3:17403200-17449200	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr3:17403400-17442200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr3:17404200-17449200	Weak transcription	Esophagus	oesophagus
22	chr3:17405000-17432400	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr3:17405200-17414200	Weak transcription	A549	lung
24	chr3:17406400-17442000	Weak transcription	Lung	lung
25	chr3:17407600-17443400	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr3:17407800-17419400	Weak transcription	Brain Hippocampus Middle	brain
27	chr3:17409200-17430800	Weak transcription	Fetal Muscle Leg	muscle
28	chr3:17409200-17435000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr3:17409400-17414400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr3:17409600-17413000	Weak transcription	HepG2	liver
31	chr3:17410000-17426800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr3:17410200-17445200	Weak transcription	Right Ventricle	heart
33	chr3:17410200-17445600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr3:17410200-17447200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr3:17410200-17451400	Weak transcription	Brain Angular Gyrus	brain
36	chr3:17410400-17443400	Weak transcription	Brain Cingulate Gyrus	brain
37	chr3:17410400-17447800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr3:17410600-17418400	Strong transcription	Primary monocytes fromperipheralblood	blood
39	chr3:17410800-17413200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr3:17410800-17414600	Strong transcription	Dnd41	blood
41	chr3:17411000-17413200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr3:17411000-17413800	Strong transcription	Primary neutrophils fromperipheralblood	blood
43	chr3:17411000-17418400	Strong transcription	Monocytes-CD14+_RO01746	blood
44	chr3:17411200-17412800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr3:17411200-17412800	Weak transcription	Placenta	Placenta
46	chr3:17411200-17414400	Weak transcription	Colon Smooth Muscle	Colon
47	chr3:17411200-17418400	Strong transcription	Primary B cells from peripheral blood	blood
48	chr3:17411200-17467400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr3:17411400-17413200	Weak transcription	Fetal Thymus	thymus
50	chr3:17411600-17414800	Weak transcription	Cortex derived primary cultured neurospheres	brain

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