Variant report

Variant	esv1803745
Chromosome Location	chr3:101196030-101230330
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:191)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:191 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:101230180-101230380	K562	blood:	n/a	chr3:101230220-101230236
2	BACH1	chr3:101203693-101203950	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr3:101203730-101203896	K562	blood:	n/a	n/a
4	BHLHE40	chr3:101198195-101198424	K562	blood:	n/a	n/a
5	BHLHE40	chr3:101230025-101230401	K562	blood:	n/a	n/a
6	CEBPB	chr3:101228713-101229032	IMR90	lung:	n/a	n/a
7	CEBPB	chr3:101200609-101200824	IMR90	lung:	n/a	chr3:101200645-101200656
8	CEBPB	chr3:101228734-101229011	K562	blood:	n/a	n/a
9	CEBPB	chr3:101200534-101200829	A549	lung:	n/a	chr3:101200645-101200656
10	CEBPB	chr3:101200619-101200839	K562	blood:	n/a	chr3:101200645-101200656
11	CEBPB	chr3:101228699-101229048	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr3:101200546-101200825	Hela-S3	cervix:	n/a	chr3:101200645-101200656
13	CEBPB	chr3:101200501-101200834	HepG2	liver:	n/a	chr3:101200645-101200656
14	CTCF	chr3:101214480-101214630	HA-sp	spinal cord:	n/a	n/a
15	CTCF	chr3:101214560-101214710	HepG2	liver:	n/a	n/a
16	CTCF	chr3:101214505-101214697	HUVEC	blood vessel:	n/a	n/a
17	CTCF	chr3:101203420-101203570	GM12864	blood:	n/a	n/a
18	CTCF	chr3:101214500-101214650	HepG2	liver:	n/a	n/a
19	CTCF	chr3:101223520-101223670	GM12873	blood:	n/a	n/a
20	CTCF	chr3:101214421-101214769	K562	blood:	n/a	n/a
21	CTCF	chr3:101214394-101214681	HepG2	liver:	n/a	n/a
22	CTCF	chr3:101214520-101214670	K562	blood:	n/a	n/a
23	CTCF	chr3:101214520-101214670	HMEC	breast:	n/a	n/a
24	CTCF	chr3:101205678-101205760	GM13976	blood:	n/a	n/a
25	CTCF	chr3:101214540-101214690	HRE	kidney:	n/a	n/a
26	CTCF	chr3:101214480-101214630	HMF	breast:	n/a	n/a
27	CTCF	chr3:101214500-101214650	GM12874	blood:	n/a	n/a
28	CTCF	chr3:101214540-101214690	HMF	breast:	n/a	n/a
29	CTCF	chr3:101214520-101214670	HAc	cerebellar:	n/a	n/a
30	CTCF	chr3:101214520-101214670	HVMF	connective:	n/a	n/a
31	CTCF	chr3:101214540-101214690	SAEC	small airway:	n/a	n/a
32	CTCF	chr3:101214520-101214670	NHEK	skin:	n/a	n/a
33	CTCF	chr3:101214495-101214680	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr3:101214481-101214714	K562	blood:	n/a	n/a
35	CTCF	chr3:101224060-101224103	GM13977	blood:	n/a	n/a
36	CTCF	chr3:101214540-101214690	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr3:101214504-101214844	MCF-7	breast:	n/a	n/a
38	CTCF	chr3:101214540-101214690	WI-38	lung:	n/a	n/a
39	CTCF	chr3:101214500-101214650	AG04450	lung:	n/a	n/a
40	CTCF	chr3:101214520-101214670	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr3:101214540-101214690	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr3:101214366-101214865	A549	lung:	n/a	n/a
43	CTCF	chr3:101214600-101214750	HVMF	connective:	n/a	n/a
44	CTCF	chr3:101214493-101214696	HepG2	liver:	n/a	n/a
45	CTCF	chr3:101214480-101214630	Caco-2	colon:	n/a	n/a
46	CTCF	chr3:101214520-101214670	GM06990	blood:	n/a	n/a
47	CTCF	chr3:101214540-101214690	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr3:101214580-101214730	A549	lung:	n/a	n/a
49	CTCF	chr3:101214520-101214670	GM12874	blood:	n/a	n/a
50	CTCF	chr3:101214480-101214630	RPTEC	kidney:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:101228308-101228358	CMK	blood:	n/a
2	chr3:101228308-101228358	SK-N-SH_RA	brain:	n/a
3	chr3:101228308-101228358	AG04449	skin:	fetal
4	chr3:101228308-101228358	NHBE	bronchial:	n/a
5	chr3:101228308-101228358	MCF10A-Er-Src	breast:	n/a
6	chr3:101228308-101228358	Caco-2	colon:	n/a
7	chr3:101228308-101228358	HCPEpiC	choroid plexus:	n/a
8	chr3:101228308-101228358	SK-N-MC	brain:	n/a
9	chr3:101228308-101228358	BJ	skin:	n/a
10	chr3:101228308-101228358	ECC-1	luminal epithelium:	n/a
11	chr3:101228308-101228358	HCM	heart:	n/a
12	chr3:101228308-101228358	MCF-7	breast:	n/a
13	chr3:101228308-101228358	IMR90	lung:	fetal
14	chr3:101228308-101228358	HUVEC	blood vessel:	n/a
15	chr3:101228308-101228358	AoSMC	blood vessel:	n/a
16	chr3:101228308-101228358	GM12878	blood:	n/a
17	chr3:101228308-101228358	HEK293	kidney:	embryo
18	chr3:101228308-101228358	GM12891	blood:	n/a
19	chr3:101228308-101228358	BE2_C	brain:	n/a
20	chr3:101228308-101228358	NB4	blood:	n/a
21	chr3:101228308-101228358	PrEC	prostate:	n/a
22	chr3:101228308-101228358	HMEC	breast:	n/a
23	chr3:101228308-101228358	GM19239	blood:	n/a
24	chr3:101228308-101228358	HL-60	blood:	n/a
25	chr3:101228308-101228358	GM12892	blood:	n/a
26	chr3:101228308-101228358	U87	brain:	n/a
27	chr3:101228308-101228358	HAEpiC	amniotic membrane:	n/a
28	chr3:101228308-101228358	SKMC	muscle:	n/a
29	chr3:101228308-101228358	HRE	kidney:	n/a
30	chr3:101228308-101228358	ProgFib	skin:	n/a
31	chr3:101228308-101228358	AG09319	gingival:	n/a
32	chr3:101228308-101228358	AG10803	skin:	n/a
33	chr3:101228308-101228358	HPAEpiC	pulmonary alveolar:	n/a
34	chr3:101228308-101228358	AG09309	skin:	n/a
35	chr3:101228308-101228358	H1-hESC	embryonic stem cell:	embryo
36	chr3:101228308-101228358	A549	lung:	n/a
37	chr3:101228308-101228358	PFSK-1	brain:	n/a
38	chr3:101228308-101228358	NH-A	brain:	n/a
39	chr3:101228308-101228358	HEEpiC	esophagus:	n/a
40	chr3:101228308-101228358	Hela-S3	cervix:	n/a
41	chr3:101228308-101228358	NT2-D1	testis:	n/a
42	chr3:101228308-101228358	AG04450	lung:	fetal
43	chr3:101228308-101228358	SAEC	small airway:	n/a
44	chr3:101228308-101228358	Jurkat	blood:	n/a
45	chr3:101228308-101228358	NHDF-neo	bronchial:	n/a
46	chr3:101228308-101228358	PANC-1	pancreas:	n/a
47	chr3:101228308-101228358	SK-N-SH	brain:	n/a
48	chr3:101228308-101228358	LNCaP	prostate:	n/a
49	chr3:101228308-101228358	RPTEC	kidney:	n/a
50	chr3:101228308-101228358	HRCEpiC	kidney:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:101217352..101220548-chr3:101224005..101228442,4	K562	blood:
2	chr3:101221906..101224392-chr3:101228561..101230240,2	K562	blood:
3	chr17:56707800..56709501-chr3:101229613..101232436,2	MCF-7	breast:
4	chr3:101212560..101214999-chr3:101290197..101292554,2	K562	blood:
5	chr3:101218206..101221093-chr3:101229989..101232899,2	K562	blood:
6	chr3:101217352..101220548-chr3:101224005..101228442,4	K562	blood:
7	chr3:101227390..101230508-chr3:101230667..101234015,4	K562	blood:
8	chr3:100118496..100120943-chr3:101229402..101232050,2	K562	blood:
9	chr3:101221906..101224392-chr3:101228561..101230240,2	K562	blood:
10	chr3:101214465..101215044-chr3:101263439..101263951,2	MCF-7	breast:
11	chr3:101227815..101230190-chr3:101280039..101282322,2	K562	blood:
12	chr3:101220719..101222487-chr3:101223167..101226043,2	K562	blood:
13	chr3:101210866..101213029-chr3:101217079..101219050,2	K562	blood:
14	chr3:101195493..101197893-chr3:101224668..101226171,2	MCF-7	breast:
15	chr3:101225556..101229482-chr3:101230162..101232900,3	MCF-7	breast:
16	chr3:101230038..101233245-chr3:101289410..101293829,6	MCF-7	breast:
17	chr3:101208401..101210494-chr3:101226740..101229607,2	MCF-7	breast:
18	chr3:101222133..101223732-chr3:101291929..101294188,2	K562	blood:
19	chr3:101195493..101197893-chr3:101224668..101226171,2	MCF-7	breast:
20	chr3:101208401..101210494-chr3:101226740..101229607,2	MCF-7	breast:
21	chr3:101230224..101236227-chr3:101287209..101294479,8	K562	blood:
22	chr3:101219595..101222487-chr3:101223167..101225401,2	K562	blood:
23	chr3:101210866..101213029-chr3:101217079..101219050,2	K562	blood:
24	chr3:101225102..101229003-chr3:101290348..101293915,4	K562	blood:
25	chr3:101227907..101233845-chr3:101279162..101282528,7	K562	blood:
26	chr3:101224426..101226291-chr3:101233090..101235403,2	K562	blood:
27	chr3:101218206..101221093-chr3:101229989..101232899,2	K562	blood:
28	chr3:101229711..101231940-chr3:101430823..101433136,2	MCF-7	breast:
29	chr3:101230042..101231916-chr3:101297585..101299542,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000238525	TF binding region
ENSG00000238525	CpG island
ENSG00000174173	chromatin interactions
ENSG00000238525	chromatin interactions
ENSG00000244119	chromatin interactions
ENSG00000081154	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000206535	chromatin interactions
ENSG00000138468	chromatin interactions
ENSG00000154174	chromatin interactions

Extended variants
information (count: 1172 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1172 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6771561	chr3:101196087-101196088	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs376957235	chr3:101196093-101196094	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs35015213	chr3:101196172-101196173	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs534795558	chr3:101196178-101196179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553017038	chr3:101196184-101196185	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568235504	chr3:101196313-101196314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs77322387	chr3:101196323-101196324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs60916302	chr3:101196343-101196344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs397752759	chr3:101196351-101196352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554349798	chr3:101196352-101196353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575678812	chr3:101196367-101196368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576244632	chr3:101196403-101196404	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537398193	chr3:101196417-101196418	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558245100	chr3:101196463-101196464	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576805556	chr3:101196466-101196467	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138945147	chr3:101196493-101196494	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs559446146	chr3:101196554-101196555	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574595927	chr3:101196592-101196593	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542433974	chr3:101196605-101196606	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563954725	chr3:101196651-101196652	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531092172	chr3:101196652-101196653	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs59085990	chr3:101196663-101196664	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs564644071	chr3:101196667-101196668	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528441863	chr3:101196678-101196679	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78801313	chr3:101196694-101196695	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75875088	chr3:101196695-101196696	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201860020	chr3:101196706-101196707	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112898887	chr3:101196708-101196709	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79217631	chr3:101196716-101196717	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs72944104	chr3:101196755-101196756	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs55774498	chr3:101196785-101196786	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs547975067	chr3:101196797-101196798	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538042881	chr3:101196800-101196801	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562688901	chr3:101196801-101196802	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569861292	chr3:101196851-101196852	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528517618	chr3:101196901-101196902	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs536931043	chr3:101196929-101196930	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs143880389	chr3:101196951-101196952	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182865875	chr3:101196952-101196953	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs148620585	chr3:101196983-101196984	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs553046362	chr3:101196994-101196995	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs574582995	chr3:101197003-101197004	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541974680	chr3:101197007-101197008	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563718635	chr3:101197013-101197014	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575762898	chr3:101197044-101197045	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs143244120	chr3:101197058-101197059	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146226663	chr3:101197109-101197110	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529958073	chr3:101197112-101197113	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528766626	chr3:101197114-101197115	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs567967320	chr3:101197150-101197151	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	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
Neurodevelopmental disorder	22521361	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
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21785460	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:824 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:101160200-101210800	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr3:101161400-101196800	Weak transcription	Thymus	Thymus
3	chr3:101161400-101207600	Weak transcription	Aorta	Aorta
4	chr3:101171200-101230400	Weak transcription	Brain Substantia Nigra	brain
5	chr3:101171400-101207800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr3:101174000-101202000	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr3:101174600-101211000	Weak transcription	Duodenum Mucosa	Duodenum
8	chr3:101176000-101211200	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr3:101176600-101211600	Weak transcription	HSMM	muscle
10	chr3:101176800-101203200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr3:101176800-101211200	Weak transcription	Stomach Smooth Muscle	stomach
12	chr3:101176800-101211400	Weak transcription	Colon Smooth Muscle	Colon
13	chr3:101177600-101210800	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr3:101177800-101202000	Weak transcription	Dnd41	blood
15	chr3:101177800-101202800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr3:101178200-101207000	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr3:101184200-101197000	Weak transcription	Small Intestine	intestine
18	chr3:101184400-101203200	Weak transcription	Ovary	ovary
19	chr3:101185800-101197800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr3:101186000-101211000	Weak transcription	Brain Anterior Caudate	brain
21	chr3:101186000-101211000	Weak transcription	Pancreas	Pancrea
22	chr3:101186000-101211000	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr3:101186200-101203200	Weak transcription	Left Ventricle	heart
24	chr3:101186200-101203400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr3:101186200-101203600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr3:101186200-101211200	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr3:101186400-101199400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr3:101186400-101202600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr3:101186400-101210600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr3:101186400-101223600	Weak transcription	Gastric	stomach
31	chr3:101186800-101196200	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr3:101186800-101196800	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr3:101186800-101197600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr3:101186800-101198000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr3:101186800-101203400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr3:101187000-101198000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr3:101187000-101211200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr3:101188200-101206800	Weak transcription	Adipose Nuclei	Adipose
39	chr3:101189000-101207000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr3:101190200-101200200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr3:101190800-101207200	Weak transcription	Fetal Intestine Large	intestine
42	chr3:101191000-101206800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr3:101191200-101201600	Weak transcription	Fetal Kidney	kidney
44	chr3:101191400-101201800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:101193200-101230400	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr3:101193600-101211400	Weak transcription	Fetal Brain Male	brain
47	chr3:101193800-101196400	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr3:101193800-101197200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr3:101193800-101201000	Weak transcription	Fetal Muscle Trunk	muscle
50	chr3:101194400-101204200	Weak transcription	Monocytes-CD14+_RO01746	blood

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