Variant report

Variant	esv14657
Chromosome Location	chr16:70234205-70284981
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1441)
CpG islands
(count:244)
Chromatin interactive
region (count:17)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1441 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr16:70252521-70252845	GM12878	blood:	n/a	chr16:70252736-70252746
2	BATF	chr16:70275352-70275629	GM12878	blood:	n/a	n/a
3	BATF	chr16:70266143-70266490	GM12878	blood:	n/a	n/a
4	BATF	chr16:70275330-70275612	GM12878	blood:	n/a	n/a
5	BATF	chr16:70242991-70243230	GM12878	blood:	n/a	n/a
6	BATF	chr16:70259711-70260057	GM12878	blood:	n/a	n/a
7	BATF	chr16:70269207-70269408	GM12878	blood:	n/a	n/a
8	BATF	chr16:70265769-70265977	GM12878	blood:	n/a	n/a
9	BATF	chr16:70266179-70266523	GM12878	blood:	n/a	n/a
10	BATF	chr16:70243288-70243494	GM12878	blood:	n/a	n/a
11	BATF	chr16:70270340-70270551	GM12878	blood:	n/a	n/a
12	BATF	chr16:70272693-70272978	GM12878	blood:	n/a	n/a
13	BATF	chr16:70277954-70278184	GM12878	blood:	n/a	n/a
14	BATF	chr16:70249268-70249471	GM12878	blood:	n/a	n/a
15	BATF	chr16:70251010-70251261	GM12878	blood:	n/a	n/a
16	BATF	chr16:70251089-70251362	GM12878	blood:	n/a	n/a
17	BATF	chr16:70274761-70275229	GM12878	blood:	n/a	n/a
18	BATF	chr16:70274531-70275234	GM12878	blood:	n/a	n/a
19	BATF	chr16:70272645-70272986	GM12878	blood:	n/a	n/a
20	BATF	chr16:70269196-70269455	GM12878	blood:	n/a	n/a
21	BCL11A	chr16:70272703-70272967	GM12878	blood:	n/a	n/a
22	BCL11A	chr16:70275340-70275579	GM12878	blood:	n/a	n/a
23	BCL11A	chr16:70274796-70275305	GM12878	blood:	n/a	n/a
24	BCL11A	chr16:70274569-70274791	GM12878	blood:	n/a	n/a
25	BCL11A	chr16:70272603-70273149	GM12878	blood:	n/a	n/a
26	BCL11A	chr16:70266128-70266474	GM12878	blood:	n/a	n/a
27	BCL11A	chr16:70260079-70260328	GM12878	blood:	n/a	n/a
28	BCL11A	chr16:70265235-70265407	GM12878	blood:	n/a	n/a
29	BCL11A	chr16:70256901-70257158	GM12878	blood:	n/a	n/a
30	BCL11A	chr16:70247717-70247954	GM12878	blood:	n/a	n/a
31	BCL11A	chr16:70249059-70249253	GM12878	blood:	n/a	n/a
32	BCL11A	chr16:70256507-70256821	GM12878	blood:	n/a	n/a
33	BCL11A	chr16:70253466-70253640	GM12878	blood:	n/a	n/a
34	BCL11A	chr16:70267253-70267439	GM12878	blood:	n/a	n/a
35	BCL11A	chr16:70266040-70266508	GM12878	blood:	n/a	n/a
36	BCL11A	chr16:70252607-70252876	GM12878	blood:	n/a	n/a
37	BCL11A	chr16:70274544-70275641	GM12878	blood:	n/a	n/a
38	BCL11A	chr16:70256979-70257253	GM12878	blood:	n/a	n/a
39	BCL11A	chr16:70252674-70252910	GM12878	blood:	n/a	n/a
40	BCL11A	chr16:70273183-70273430	GM12878	blood:	n/a	n/a
41	BCL11A	chr16:70242982-70243227	GM12878	blood:	n/a	n/a
42	BCL11A	chr16:70264796-70265164	GM12878	blood:	n/a	n/a
43	BHLHE40	chr16:70247348-70248139	HepG2	liver:	n/a	n/a
44	BHLHE40	chr16:70242201-70242419	HepG2	liver:	n/a	n/a
45	BHLHE40	chr16:70284901-70285174	K562	blood:	n/a	n/a
46	BHLHE40	chr16:70256452-70256822	HepG2	liver:	n/a	n/a
47	BHLHE40	chr16:70260045-70260625	HepG2	liver:	n/a	n/a
48	BHLHE40	chr16:70249020-70249505	HepG2	liver:	n/a	n/a
49	BHLHE40	chr16:70254937-70255237	HepG2	liver:	n/a	n/a
50	BHLHE40	chr16:70242942-70243167	HepG2	liver:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70283421-70283471	HCF	heart:	n/a
2	chr16:70284928-70284978	SAEC	small airway:	n/a
3	chr16:70284893-70284943	HCM	heart:	n/a
4	chr16:70284893-70284943	MCF-7	breast:	n/a
5	chr16:70284928-70284978	HCPEpiC	choroid plexus:	n/a
6	chr16:70284893-70284943	GM12878	blood:	n/a
7	chr16:70284928-70284978	MCF10A-Er-Src	breast:	n/a
8	chr16:70284893-70284943	NHDF-neo	bronchial:	n/a
9	chr16:70259186-70259236	MCF-7	breast:	n/a
10	chr16:70259186-70259236	HEEpiC	esophagus:	n/a
11	chr16:70283421-70283471	BJ	skin:	n/a
12	chr16:70284928-70284978	MCF-7	breast:	n/a
13	chr16:70284928-70284978	BJ	skin:	n/a
14	chr16:70259186-70259236	IMR90	lung:	fetal
15	chr16:70284928-70284978	AG10803	skin:	n/a
16	chr16:70284893-70284943	AG10803	skin:	n/a
17	chr16:70284893-70284943	ECC-1	luminal epithelium:	n/a
18	chr16:70259186-70259236	PrEC	prostate:	n/a
19	chr16:70284893-70284943	AG04450	lung:	fetal
20	chr16:70284928-70284978	HUVEC	blood vessel:	n/a
21	chr16:70284893-70284943	AG09319	gingival:	n/a
22	chr16:70283421-70283471	K562	blood:	n/a
23	chr16:70283421-70283471	HNPCEpiC	eye:	n/a
24	chr16:70283421-70283471	GM06990	blood:	n/a
25	chr16:70284928-70284978	HAEpiC	amniotic membrane:	n/a
26	chr16:70259186-70259236	BJ	skin:	n/a
27	chr16:70284893-70284943	HRPEpiC	eye:	n/a
28	chr16:70259186-70259236	LNCaP	prostate:	n/a
29	chr16:70284893-70284943	GM06990	blood:	n/a
30	chr16:70259186-70259236	Hepatocyte	liver:	n/a
31	chr16:70284893-70284943	Jurkat	blood:	n/a
32	chr16:70259186-70259236	NHDF-neo	bronchial:	n/a
33	chr16:70283421-70283471	GM12878	blood:	n/a
34	chr16:70284928-70284978	AG04450	lung:	fetal
35	chr16:70283421-70283471	NH-A	brain:	n/a
36	chr16:70284928-70284978	AG09309	skin:	n/a
37	chr16:70284928-70284978	HRCEpiC	kidney:	n/a
38	chr16:70284893-70284943	HRCEpiC	kidney:	n/a
39	chr16:70284893-70284943	GM19239	blood:	n/a
40	chr16:70284893-70284943	Hela-S3	cervix:	n/a
41	chr16:70284928-70284978	NH-A	brain:	n/a
42	chr16:70283421-70283471	HepG2	liver:	n/a
43	chr16:70284893-70284943	HPAEpiC	pulmonary alveolar:	n/a
44	chr16:70284928-70284978	NB4	blood:	n/a
45	chr16:70283421-70283471	CMK	blood:	n/a
46	chr16:70259186-70259236	ovcar-3	ovarian:	n/a
47	chr16:70259186-70259236	T-47D	breast:	n/a
48	chr16:70259186-70259236	AG04450	lung:	fetal
49	chr16:70283421-70283471	HCT-116	colon:	n/a
50	chr16:70284928-70284978	PFSK-1	brain:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:70284511..70286776-chr16:70330314..70334173,3	MCF-7	breast:
2	chr16:70279244..70282169-chr16:70284255..70286230,4	K562	blood:
3	chr16:70284251..70286200-chr16:70298122..70301114,5	MCF-7	breast:
4	chr16:70279273..70282169-chr16:70284255..70286204,3	K562	blood:
5	chr16:70283799..70285737-chr6:44213868..44216847,2	K562	blood:
6	chr16:70284271..70287113-chr16:70301564..70303205,2	MCF-7	breast:
7	chr16:70283625..70285831-chr16:70321379..70323186,2	K562	blood:
8	chr16:70279244..70282169-chr16:70284255..70286230,4	K562	blood:
9	chr16:70278247..70283453-chr16:70284015..70287841,6	MCF-7	breast:
10	chr16:70284942..70287057-chr16:70291525..70294943,4	K562	blood:
11	chr16:70279273..70282169-chr16:70284255..70286204,3	K562	blood:
12	chr16:70284207..70286196-chr16:70321648..70323975,3	MCF-7	breast:
13	chr16:70283970..70285913-chr16:70380669..70382950,2	K562	blood:
14	chr16:70284505..70286615-chr16:70556732..70559559,2	MCF-7	breast:
15	chr16:70278247..70283453-chr16:70284015..70287841,6	MCF-7	breast:
16	chr16:70245449..70247912-chr16:70284379..70285973,2	MCF-7	breast:
17	chr16:70191657..70193675-chr16:70283732..70285560,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DDX19B-2	chr16:70280560-70282018	NONHSAT143414
2	lnc-DDX19B-2	chr16:70273803-70273904	NONHSAT143414

No data

Variant related genes	Relation type
ENSG00000238734	TF binding region
ENSG00000269866	TF binding region
ENSG00000269746	TF binding region
ENSG00000261145	TF binding region
ENSG00000261556	TF binding region
ENSG00000238734	CpG island
ENSG00000269866	CpG island
ENSG00000269746	CpG island
ENSG00000261145	CpG island
ENSG00000261556	CpG island
ENSG00000157349	chromatin interactions
ENSG00000103051	chromatin interactions
ENSG00000168872	chromatin interactions
ENSG00000096384	chromatin interactions
ENSG00000261556	chromatin interactions
ENSG00000265230	chromatin interactions
ENSG00000260537	chromatin interactions
ENSG00000223496	chromatin interactions
ENSG00000189091	chromatin interactions
ENSG00000090861	chromatin interactions

Extended variants
information (count: 1975 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1975 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547586697	chr16:70234222-70234223	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs565601149	chr16:70234242-70234243	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs539526457	chr16:70234262-70234263	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs551083880	chr16:70234286-70234287	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs147097777	chr16:70234290-70234291	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs4011567	chr16:70234302-70234303	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs143469552	chr16:70234303-70234304	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs569349555	chr16:70234359-70234360	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs113558590	chr16:70234471-70234472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368361451	chr16:70234497-70234498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537331596	chr16:70234557-70234558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555666105	chr16:70234640-70234641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574015729	chr16:70234644-70234645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113472492	chr16:70234952-70234953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369343494	chr16:70234969-70234970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs75957471	chr16:70235080-70235081	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs568232845	chr16:70235145-70235146	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs199544972	chr16:70235187-70235188	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs534870839	chr16:70235516-70235517	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs192870936	chr16:70235521-70235522	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs553541487	chr16:70235546-70235547	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs111514643	chr16:70235682-70235683	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs146294586	chr16:70235720-70235721	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs545526032	chr16:70235728-70235729	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs369788978	chr16:70235743-70235744	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs563658119	chr16:70235760-70235761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373463516	chr16:70235870-70235871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs556303444	chr16:70235893-70235894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs377315560	chr16:70235894-70235895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575738493	chr16:70235898-70235899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376911274	chr16:70235922-70235923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543068090	chr16:70235929-70235930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561932640	chr16:70235971-70235972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs3874602	chr16:70235983-70235984	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
35	rs547231800	chr16:70235984-70235985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559542956	chr16:70235992-70235993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556402798	chr16:70236041-70236042	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs532873968	chr16:70236061-70236062	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs570462984	chr16:70236094-70236095	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs569287008	chr16:70236101-70236102	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs536620125	chr16:70236220-70236221	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs548583813	chr16:70236287-70236288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs62049374	chr16:70236299-70236300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567578471	chr16:70236308-70236309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535329269	chr16:70236340-70236341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553282953	chr16:70236352-70236353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377543473	chr16:70236377-70236378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs578150298	chr16:70236403-70236404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370811271	chr16:70236412-70236413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538736693	chr16:70236439-70236440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	21909424	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	20841430	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70226600-70252600	Weak transcription	Adipose Nuclei	Adipose
2	chr16:70231200-70252000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr16:70231400-70258600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr16:70232400-70284800	Weak transcription	Spleen	Spleen
5	chr16:70232600-70241400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr16:70233200-70246600	Weak transcription	Fetal Stomach	stomach
7	chr16:70233200-70253600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr16:70233200-70283400	Weak transcription	Primary hematopoietic stem cells	blood
9	chr16:70233200-70283600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr16:70233400-70235400	Weak transcription	Brain Substantia Nigra	brain
11	chr16:70233600-70246600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr16:70233600-70253600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr16:70233800-70238600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr16:70233800-70252200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr16:70234800-70260800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr16:70235600-70241000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr16:70235600-70247400	Weak transcription	Fetal Intestine Small	intestine
18	chr16:70235600-70258600	Weak transcription	Pancreas	Pancrea
19	chr16:70235600-70284200	Weak transcription	Brain Cingulate Gyrus	brain
20	chr16:70236200-70258600	Weak transcription	Thymus	Thymus
21	chr16:70237000-70237200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr16:70237000-70237200	Enhancers	Sigmoid Colon	Sigmoid Colon
23	chr16:70237000-70258600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr16:70237000-70258800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr16:70237200-70247000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr16:70237200-70267200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr16:70237200-70284800	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr16:70238200-70240000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr16:70238400-70240000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr16:70238400-70246200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr16:70238400-70253400	Weak transcription	Duodenum Mucosa	Duodenum
32	chr16:70238400-70274600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr16:70238600-70247200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr16:70238600-70252200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr16:70238600-70284800	Weak transcription	Esophagus	oesophagus
36	chr16:70238800-70252200	Weak transcription	Primary B cells from peripheral blood	blood
37	chr16:70238800-70253400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr16:70238800-70260400	Weak transcription	Fetal Brain Female	brain
39	chr16:70238800-70283400	Weak transcription	NHEK	skin
40	chr16:70238800-70283600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr16:70239000-70260600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr16:70239000-70266800	Weak transcription	Aorta	Aorta
43	chr16:70239200-70256800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr16:70239200-70260600	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr16:70239600-70240000	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr16:70239600-70246200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr16:70239600-70246600	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr16:70239600-70247600	Weak transcription	Fetal Intestine Large	intestine
49	chr16:70239600-70283400	Weak transcription	Brain Angular Gyrus	brain
50	chr16:70239800-70247200	Weak transcription	Dnd41	blood

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