Variant report

Variant	esv1825225
Chromosome Location	chr16:30258820-30303402
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1902)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1902 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr16:30289855-30290073	K562	blood:	n/a	n/a
2	BATF	chr16:30299474-30300218	GM12878	blood:	n/a	n/a
3	BATF	chr16:30302951-30303210	GM12878	blood:	n/a	n/a
4	BATF	chr16:30298130-30298375	GM12878	blood:	n/a	n/a
5	BATF	chr16:30258549-30259033	GM12878	blood:	n/a	n/a
6	BATF	chr16:30289863-30290214	GM12878	blood:	n/a	chr16:30290044-30290055
7	BATF	chr16:30281694-30281983	GM12878	blood:	n/a	n/a
8	BATF	chr16:30299549-30300244	GM12878	blood:	n/a	n/a
9	BATF	chr16:30289456-30289664	GM12878	blood:	n/a	n/a
10	BATF	chr16:30300748-30300974	GM12878	blood:	n/a	n/a
11	BATF	chr16:30274122-30274547	GM12878	blood:	n/a	n/a
12	BATF	chr16:30300762-30300954	GM12878	blood:	n/a	n/a
13	BATF	chr16:30300239-30300587	GM12878	blood:	n/a	n/a
14	BATF	chr16:30280187-30280431	GM12878	blood:	n/a	n/a
15	BATF	chr16:30298135-30298343	GM12878	blood:	n/a	n/a
16	BATF	chr16:30297566-30297916	GM12878	blood:	n/a	n/a
17	BATF	chr16:30276188-30276522	GM12878	blood:	n/a	chr16:30276391-30276402
18	BATF	chr16:30277514-30277795	GM12878	blood:	n/a	n/a
19	BATF	chr16:30259201-30259411	GM12878	blood:	n/a	n/a
20	BATF	chr16:30268107-30268387	GM12878	blood:	n/a	n/a
21	BATF	chr16:30289459-30289741	GM12878	blood:	n/a	n/a
22	BATF	chr16:30274116-30274392	GM12878	blood:	n/a	n/a
23	BATF	chr16:30281598-30281838	GM12878	blood:	n/a	n/a
24	BATF	chr16:30288532-30288733	GM12878	blood:	n/a	n/a
25	BATF	chr16:30283247-30283707	GM12878	blood:	n/a	n/a
26	BATF	chr16:30300298-30300596	GM12878	blood:	n/a	n/a
27	BATF	chr16:30288879-30289097	GM12878	blood:	n/a	n/a
28	BATF	chr16:30268701-30268945	GM12878	blood:	n/a	n/a
29	BATF	chr16:30277626-30277987	GM12878	blood:	n/a	n/a
30	BATF	chr16:30297523-30297979	GM12878	blood:	n/a	n/a
31	BATF	chr16:30287185-30287579	GM12878	blood:	n/a	n/a
32	BATF	chr16:30292841-30293135	GM12878	blood:	n/a	n/a
33	BATF	chr16:30296504-30296687	GM12878	blood:	n/a	n/a
34	BATF	chr16:30289827-30290210	GM12878	blood:	n/a	chr16:30290044-30290055
35	BCL11A	chr16:30276155-30276510	GM12878	blood:	n/a	chr16:30276462-30276471
36	BCL11A	chr16:30272893-30273062	GM12878	blood:	n/a	n/a
37	BCL11A	chr16:30268492-30268693	GM12878	blood:	n/a	n/a
38	BCL11A	chr16:30278360-30278686	GM12878	blood:	n/a	n/a
39	BCL11A	chr16:30283520-30283675	GM12878	blood:	n/a	n/a
40	BCL11A	chr16:30288560-30288762	GM12878	blood:	n/a	n/a
41	BCL11A	chr16:30289460-30289663	GM12878	blood:	n/a	n/a
42	BCL11A	chr16:30300749-30301042	GM12878	blood:	n/a	n/a
43	BCL11A	chr16:30292806-30293135	GM12878	blood:	n/a	n/a
44	BCL11A	chr16:30281467-30281965	GM12878	blood:	n/a	n/a
45	BCL11A	chr16:30282579-30282749	GM12878	blood:	n/a	n/a
46	BCL11A	chr16:30282125-30282350	GM12878	blood:	n/a	n/a
47	BCL11A	chr16:30289814-30290161	GM12878	blood:	n/a	n/a
48	BCL11A	chr16:30297600-30297978	GM12878	blood:	n/a	n/a
49	BCL11A	chr16:30281534-30281971	GM12878	blood:	n/a	n/a
50	BCL11A	chr16:30289424-30289742	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:30293906-30293956	NHBE	bronchial:	n/a
2	chr16:30293906-30293956	HPAEpiC	pulmonary alveolar:	n/a
3	chr16:30293906-30293956	MCF10A-Er-Src	breast:	n/a
4	chr16:30293906-30293956	Jurkat	blood:	n/a
5	chr16:30293906-30293956	ECC-1	luminal epithelium:	n/a
6	chr16:30293906-30293956	HNPCEpiC	eye:	n/a
7	chr16:30293906-30293956	Caco-2	colon:	n/a
8	chr16:30293906-30293956	HCM	heart:	n/a
9	chr16:30293906-30293956	K562	blood:	n/a
10	chr16:30293906-30293956	AG04450	lung:	fetal
11	chr16:30293906-30293956	T-47D	breast:	n/a
12	chr16:30293906-30293956	HEEpiC	esophagus:	n/a
13	chr16:30293906-30293956	PANC-1	pancreas:	n/a
14	chr16:30293906-30293956	HCT-116	colon:	n/a
15	chr16:30293906-30293956	SAEC	small airway:	n/a
16	chr16:30293906-30293956	PrEC	prostate:	n/a
17	chr16:30293906-30293956	GM19239	blood:	n/a
18	chr16:30293906-30293956	HIPEpiC	eye:	n/a
19	chr16:30293906-30293956	Hela-S3	cervix:	n/a
20	chr16:30293906-30293956	HCPEpiC	choroid plexus:	n/a
21	chr16:30293906-30293956	H1-hESC	embryonic stem cell:	embryo
22	chr16:30293906-30293956	AG09309	skin:	n/a
23	chr16:30293906-30293956	NB4	blood:	n/a
24	chr16:30293906-30293956	HEK293	kidney:	embryo
25	chr16:30293906-30293956	HRE	kidney:	n/a
26	chr16:30293906-30293956	GM12891	blood:	n/a
27	chr16:30293906-30293956	Hepatocyte	liver:	n/a
28	chr16:30293906-30293956	MCF-7	breast:	n/a
29	chr16:30293906-30293956	HRCEpiC	kidney:	n/a
30	chr16:30293906-30293956	ovcar-3	ovarian:	n/a
31	chr16:30293906-30293956	GM12892	blood:	n/a
32	chr16:30293906-30293956	AG10803	skin:	n/a
33	chr16:30293906-30293956	HUVEC	blood vessel:	n/a
34	chr16:30293906-30293956	ProgFib	skin:	n/a
35	chr16:30293906-30293956	HL-60	blood:	n/a
36	chr16:30293906-30293956	PFSK-1	brain:	n/a
37	chr16:30293906-30293956	BE2_C	brain:	n/a
38	chr16:30293906-30293956	AG09319	gingival:	n/a
39	chr16:30293906-30293956	CMK	blood:	n/a
40	chr16:30293906-30293956	HRPEpiC	eye:	n/a
41	chr16:30293906-30293956	AoSMC	blood vessel:	n/a
42	chr16:30293906-30293956	NHDF-neo	bronchial:	n/a
43	chr16:30293906-30293956	AG04449	skin:	fetal
44	chr16:30293906-30293956	SKMC	muscle:	n/a
45	chr16:30293906-30293956	SK-N-SH_RA	brain:	n/a
46	chr16:30293906-30293956	NH-A	brain:	n/a
47	chr16:30293906-30293956	GM12878	blood:	n/a
48	chr16:30293906-30293956	HCF	heart:	n/a
49	chr16:30293906-30293956	HAEpiC	amniotic membrane:	n/a
50	chr16:30293906-30293956	IMR90	lung:	fetal

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SULT1A3.1-5	chr16:30275575-30275822	expReg_chr16_4358_+

No data

Variant related genes	Relation type
ENSG00000198064	TF binding region
ENSG00000239114	TF binding region
ENSG00000183604	TF binding region
ENSG00000198064	CpG island
ENSG00000239114	CpG island
ENSG00000183604	CpG island

Extended variants
information (count: 195 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:195 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11860311	chr16:30260495-30260496	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs370694817	chr16:30266880-30266881	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs375549137	chr16:30267309-30267310	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs568791873	chr16:30268720-30268721	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs536269476	chr16:30268775-30268776	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs554522974	chr16:30268781-30268782	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs566770124	chr16:30268796-30268797	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs533731714	chr16:30268839-30268840	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs368409051	chr16:30268963-30268964	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs374506260	chr16:30269016-30269017	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs113343335	chr16:30269161-30269162	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs112124150	chr16:30270751-30270752	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs111813001	chr16:30273957-30273958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs62055398	chr16:30274131-30274132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs62055399	chr16:30274138-30274139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377449278	chr16:30274623-30274624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371240215	chr16:30274690-30274691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374990914	chr16:30274947-30274948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560580969	chr16:30274966-30274967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528030776	chr16:30274978-30274979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs199590967	chr16:30275009-30275010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372189428	chr16:30275154-30275155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546413522	chr16:30275192-30275193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200413075	chr16:30275244-30275245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564695484	chr16:30275441-30275442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200952637	chr16:30275456-30275457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145245502	chr16:30275471-30275472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532226115	chr16:30275490-30275491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550367441	chr16:30275525-30275526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs3874469	chr16:30276139-30276140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568939507	chr16:30278656-30278657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529620437	chr16:30278747-30278748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375050412	chr16:30278810-30278811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368515388	chr16:30278826-30278827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111654517	chr16:30278843-30278844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs202240976	chr16:30280782-30280783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375165011	chr16:30280818-30280819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566653382	chr16:30280835-30280836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533864928	chr16:30280852-30280853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558316034	chr16:30280876-30280877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570278186	chr16:30282992-30282993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs199850092	chr16:30283284-30283285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537670717	chr16:30283364-30283365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112740439	chr16:30284304-30284305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112925912	chr16:30285338-30285339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556335860	chr16:30285710-30285711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574885040	chr16:30286065-30286066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541848362	chr16:30286303-30286304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562894424	chr16:30286365-30286366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139357160	chr16:30286387-30286388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:126)

Disease	PMID	Source
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic myeloid leukemia	21384125	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30273600-30295400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr16:30277200-30288000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr16:30277800-30287400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr16:30277800-30287600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr16:30277800-30287600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr16:30277800-30287600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr16:30277800-30287600	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr16:30277800-30287600	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr16:30277800-30287600	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr16:30277800-30287600	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr16:30277800-30287600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr16:30277800-30287600	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr16:30277800-30287600	Weak transcription	Fetal Brain Female	brain
14	chr16:30277800-30287600	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr16:30278000-30287800	Weak transcription	Adipose Nuclei	Adipose
16	chr16:30278000-30289600	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr16:30278000-30289600	Weak transcription	Fetal Thymus	thymus
18	chr16:30278000-30289600	Weak transcription	Left Ventricle	heart
19	chr16:30278000-30290200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr16:30278000-30294200	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr16:30278000-30295800	Weak transcription	Thymus	Thymus
22	chr16:30278000-30314800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr16:30278000-30319600	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr16:30278000-30319800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr16:30278000-30320200	Weak transcription	Primary B cells from peripheral blood	blood
26	chr16:30278200-30287600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr16:30278200-30289600	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr16:30278200-30290000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr16:30278200-30290000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr16:30278600-30319600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr16:30281200-30287600	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr16:30286000-30287600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr16:30286000-30288000	Weak transcription	Placenta	Placenta
34	chr16:30286000-30345400	Weak transcription	Fetal Stomach	stomach
35	chr16:30286200-30287800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr16:30286200-30287800	Weak transcription	Duodenum Mucosa	Duodenum
37	chr16:30286200-30289600	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr16:30286200-30295200	Weak transcription	Fetal Muscle Trunk	muscle
39	chr16:30286200-30297000	Weak transcription	Stomach Smooth Muscle	stomach
40	chr16:30286200-30317600	Weak transcription	Brain Cingulate Gyrus	brain
41	chr16:30286400-30288000	Weak transcription	Colon Smooth Muscle	Colon
42	chr16:30286400-30289600	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr16:30286400-30327800	Weak transcription	Fetal Intestine Small	intestine
44	chr16:30286600-30289200	Weak transcription	Brain Germinal Matrix	brain
45	chr16:30286600-30294600	Weak transcription	Colonic Mucosa	Colon
46	chr16:30286600-30295800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr16:30286600-30297800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr16:30286800-30289000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr16:30286800-30289000	Weak transcription	Fetal Intestine Large	intestine
50	chr16:30287000-30289400	Weak transcription	Brain Anterior Caudate	brain

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