Variant report
Variant | nsv1046923 |
---|---|
Chromosome Location | chr13:64321869-64419179 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:170)
- CpG islands (count:1038)
- Chromatin interactive region (count:0)
- LncRNA region (count:16)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | CEBPB | chr13:64409212-64409411 | IMR90 | lung: | n/a | chr13:64409350-64409361 |
2 | CEBPB | chr13:64409209-64409369 | HepG2 | liver: | n/a | chr13:64409350-64409361 |
3 | CEBPB | chr13:64409210-64409420 | A549 | lung: | n/a | chr13:64409350-64409361 |
4 | CHD2 | chr13:64385983-64386021 | K562 | blood: | n/a | n/a |
5 | CTCF | chr13:64324133-64324244 | ProgFib | skin: | n/a | n/a |
6 | CTCF | chr13:64403907-64404012 | HUVEC | blood vessel: | n/a | n/a |
7 | CTCF | chr13:64403823-64404050 | MCF-7 | breast: | n/a | n/a |
8 | CTCF | chr13:64324126-64324196 | HUVEC | blood vessel: | n/a | n/a |
9 | CTCF | chr13:64403812-64404067 | MCF-7 | breast: | n/a | n/a |
10 | CTCF | chr13:64338648-64338715 | Kidney_OC | kidney: | n/a | n/a |
11 | CTCF | chr13:64388012-64388076 | MCF-7 | breast: | n/a | n/a |
12 | CTCF | chr13:64324118-64324236 | GM13977 | blood: | n/a | n/a |
13 | CTCF | chr13:64324094-64324161 | K562 | blood: | n/a | n/a |
14 | CTCF | chr13:64403833-64404058 | Medullo | brain: | n/a | n/a |
15 | CTCF | chr13:64404781-64404867 | LNCaP | prostate: | n/a | n/a |
16 | CTCF | chr13:64377845-64377936 | GM13976 | blood: | n/a | n/a |
17 | CTCF | chr13:64324117-64324248 | GM10266 | blood: | n/a | n/a |
18 | CTCF | chr13:64403849-64403978 | MCF-7 | breast: | n/a | n/a |
19 | CTCF | chr13:64403878-64404005 | Pancreas_OC | pancreas: | n/a | n/a |
20 | CTCF | chr13:64324024-64324308 | K562 | blood: | n/a | n/a |
21 | CTCF | chr13:64324052-64324317 | LNCaP | prostate: | n/a | n/a |
22 | CTCF | chr13:64403870-64403967 | GM19240 | blood: | n/a | n/a |
23 | CTCF | chr13:64338496-64338540 | ProgFib | skin: | n/a | n/a |
24 | CTCF | chr13:64338485-64338489 | ProgFib | skin: | n/a | n/a |
25 | CTCF | chr13:64403907-64403977 | K562 | blood: | n/a | n/a |
26 | CTCF | chr13:64403881-64404014 | GM13976 | blood: | n/a | n/a |
27 | CTCF | chr13:64324097-64324217 | Spleen_OC | spleen: | n/a | n/a |
28 | CTCF | chr13:64403936-64403999 | Spleen_OC | spleen: | n/a | n/a |
29 | CTCF | chr13:64334444-64334532 | Spleen_OC | spleen: | n/a | n/a |
30 | CTCF | chr13:64324040-64324265 | HepG2 | liver: | n/a | n/a |
31 | CTCF | chr13:64338203-64338280 | GM13976 | blood: | n/a | n/a |
32 | CTCF | chr13:64415903-64415950 | LNCaP | prostate: | n/a | n/a |
33 | CTCF | chr13:64324092-64324260 | MCF-7 | breast: | n/a | n/a |
34 | CTCF | chr13:64330862-64330927 | Medullo | brain: | n/a | n/a |
35 | CTCF | chr13:64403878-64404020 | GM13977 | blood: | n/a | n/a |
36 | CTCF | chr13:64384593-64384675 | Lung_OC | lung: | n/a | n/a |
37 | CTCF | chr13:64324080-64324269 | Kidney_OC | kidney: | n/a | n/a |
38 | CTCF | chr13:64388076-64388141 | Fibrobl | skin: | n/a | n/a |
39 | CTCF | chr13:64403897-64403955 | H1-hESC | embryonic stem cell: | n/a | n/a |
40 | CTCF | chr13:64324197-64324224 | GM19240 | blood: | n/a | n/a |
41 | CTCF | chr13:64324125-64324255 | Fibrobl | skin: | n/a | n/a |
42 | CTCF | chr13:64403855-64404062 | Kidney_OC | kidney: | n/a | n/a |
43 | CTCF | chr13:64403767-64404058 | A549 | lung: | n/a | n/a |
44 | CTCF | chr13:64408429-64408453 | H1-hESC | embryonic stem cell: | n/a | n/a |
45 | CTCF | chr13:64339091-64339163 | Lung_OC | lung: | n/a | n/a |
46 | CTCF | chr13:64324142-64324254 | A549 | lung: | n/a | n/a |
47 | CTCF | chr13:64324108-64324265 | MCF-7 | breast: | n/a | n/a |
48 | CTCF | chr13:64388099-64388105 | MCF-7 | breast: | n/a | n/a |
49 | CTCF | chr13:64324173-64324251 | GM12878 | blood: | n/a | n/a |
50 | CTCF | chr13:64324072-64324260 | Hela-S3 | cervix: | n/a | n/a |
No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr13:64418337-64418387 | LNCaP | prostate: | n/a |
2 | chr13:64418337-64418387 | LNCaP | prostate: | n/a |
3 | chr13:64382075-64382125 | H1-hESC | embryonic stem cell: | embryo |
4 | chr13:64415303-64415353 | Hepatocyte | liver: | n/a |
5 | chr13:64415303-64415353 | Caco-2 | colon: | n/a |
6 | chr13:64388106-64388156 | HRPEpiC | eye: | n/a |
7 | chr13:64384119-64384169 | Jurkat | blood: | n/a |
8 | chr13:64388106-64388156 | SK-N-SH_RA | brain: | n/a |
9 | chr13:64418345-64418395 | SK-N-MC | brain: | n/a |
10 | chr13:64418337-64418387 | HL-60 | blood: | n/a |
11 | chr13:64385720-64385770 | NHDF-neo | bronchial: | n/a |
12 | chr13:64386020-64386070 | AG09319 | gingival: | n/a |
13 | chr13:64385881-64385931 | HPAEpiC | pulmonary alveolar: | n/a |
14 | chr13:64418345-64418395 | AG04450 | lung: | fetal |
15 | chr13:64418345-64418395 | NHDF-neo | bronchial: | n/a |
16 | chr13:64418676-64418726 | HRPEpiC | eye: | n/a |
17 | chr13:64418676-64418726 | BJ | skin: | n/a |
18 | chr13:64418676-64418726 | HCPEpiC | choroid plexus: | n/a |
19 | chr13:64385881-64385931 | BJ | skin: | n/a |
20 | chr13:64412172-64412222 | HNPCEpiC | eye: | n/a |
21 | chr13:64416816-64416866 | ovcar-3 | ovarian: | n/a |
22 | chr13:64418279-64418329 | SK-N-MC | brain: | n/a |
23 | chr13:64385720-64385770 | Caco-2 | colon: | n/a |
24 | chr13:64411884-64411934 | HAEpiC | amniotic membrane: | n/a |
25 | chr13:64418345-64418395 | ProgFib | skin: | n/a |
26 | chr13:64408172-64408222 | HRE | kidney: | n/a |
27 | chr13:64412172-64412222 | AG09309 | skin: | n/a |
28 | chr13:64416816-64416866 | SK-N-SH | brain: | n/a |
29 | chr13:64386291-64386341 | HepG2 | liver: | n/a |
30 | chr13:64386020-64386070 | RPTEC | kidney: | n/a |
31 | chr13:64416816-64416866 | NHBE | bronchial: | n/a |
32 | chr13:64411884-64411934 | ECC-1 | luminal epithelium: | n/a |
33 | chr13:64418279-64418329 | MCF-7 | breast: | n/a |
34 | chr13:64382075-64382125 | HMEC | breast: | n/a |
35 | chr13:64412172-64412222 | CMK | blood: | n/a |
36 | chr13:64412172-64412222 | AG10803 | skin: | n/a |
37 | chr13:64411884-64411934 | SKMC | muscle: | n/a |
38 | chr13:64418279-64418329 | LNCaP | prostate: | n/a |
39 | chr13:64418678-64418728 | HNPCEpiC | eye: | n/a |
40 | chr13:64382075-64382125 | HCT-116 | colon: | n/a |
41 | chr13:64412172-64412222 | HPAEpiC | pulmonary alveolar: | n/a |
42 | chr13:64382075-64382125 | SK-N-SH | brain: | n/a |
43 | chr13:64418676-64418726 | GM19239 | blood: | n/a |
44 | chr13:64418279-64418329 | SAEC | small airway: | n/a |
45 | chr13:64418337-64418387 | AoSMC | blood vessel: | n/a |
46 | chr13:64415303-64415353 | HEEpiC | esophagus: | n/a |
47 | chr13:64418676-64418726 | Jurkat | blood: | n/a |
48 | chr13:64418676-64418726 | MCF10A-Er-Src | breast: | n/a |
49 | chr13:64382075-64382125 | RPTEC | kidney: | n/a |
50 | chr13:64385720-64385770 | AG09319 | gingival: | n/a |
No data |
(count:16 , 50 per page) page:
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-PCDH20-10 | chr13:64405587-64405985 | ENSG00000219926.6 |
2 | lnc-PCDH20-10 | chr13:64402902-64403292 | ENSG00000219926.3 |
3 | lnc-PCDH20-10 | chr13:64402973-64403285 | ENSG00000219926.6 |
4 | lnc-AL445989.1-1 | chr13:64324837-64325213 | ENSG00000237378 |
5 | lnc-PCDH20-10 | chr13:64405587-64405985 | NONHSAT034184 |
6 | lnc-PCDH20-10 | chr13:64403127-64403285 | NONHSAT034184 |
7 | lnc-PCDH20-10 | chr13:64413882-64414219 | NONHSAT034181 |
8 | lnc-AL445989.1-21 | chr13:64411166-64411589 | NONHSAT034186 |
9 | lnc-PCDH20-10 | chr13:64412293-64412877 | NONHSAT034185 |
10 | lnc-PCDH20-10 | chr13:64413203-64413330 | NONHSAT034187 |
11 | lnc-PCDH20-10 | chr13:64411124-64411575 | NONHSAT034185 |
12 | lnc-PCDH20-10 | chr13:64405587-64405660 | NONHSAT034181 |
13 | lnc-PCDH20-10 | chr13:64412250-64412371 | NONHSAT034187 |
14 | lnc-PCDH20-10 | chr13:64402967-64403285 | NONHSAT034181 |
15 | lnc-PCDH20-10 | chr13:64405587-64405985 | ENSG00000219926.3 |
16 | lnc-AL445989.1-1 | chr13:64322132-64322530 | ENSG00000237378 |
No data |
No data |
Variant related genes | Relation type |
---|---|
RNU6-81P | TF binding region |
ENSG00000272299 | TF binding region |
ENSG00000219926 | TF binding region |
PPP1R2P10 | TF binding region |
ENSG00000237378 | TF binding region |
OR7E104P | TF binding region |
RNU6-81P | CpG island |
ENSG00000272299 | CpG island |
ENSG00000219926 | CpG island |
PPP1R2P10 | CpG island |
ENSG00000237378 | CpG island |
OR7E104P | CpG island |
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs535987476 | chr13:64322266-64322267 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
2 | rs535489980 | chr13:64322348-64322349 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
3 | rs370758458 | chr13:64322378-64322379 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
4 | rs9571029 | chr13:64322382-64322383 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
5 | rs572064067 | chr13:64322395-64322396 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
6 | rs545905703 | chr13:64322400-64322401 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
7 | rs2635894 | chr13:64322420-64322421 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
8 | rs564595236 | chr13:64322426-64322427 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
9 | rs9571030 | chr13:64322473-64322474 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
10 | rs2635895 | chr13:64322489-64322490 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
11 | rs9564106 | chr13:64347431-64347432 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
12 | rs538567018 | chr13:64347434-64347435 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
13 | rs557213231 | chr13:64347439-64347440 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
14 | rs74090257 | chr13:64347533-64347534 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
15 | rs535825286 | chr13:64347567-64347568 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
16 | rs550545831 | chr13:64347613-64347614 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
17 | rs554282042 | chr13:64347645-64347646 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
18 | rs143513652 | chr13:64347677-64347678 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
19 | rs192288794 | chr13:64347748-64347749 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
20 | rs12864852 | chr13:64347789-64347790 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
21 | rs114696459 | chr13:64347802-64347803 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
22 | rs185094595 | chr13:64347805-64347806 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
23 | rs140508967 | chr13:64347811-64347812 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
24 | rs12864850 | chr13:64347820-64347821 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
25 | rs144169968 | chr13:64347856-64347857 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
26 | rs545416251 | chr13:64347861-64347862 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
27 | rs151205991 | chr13:64347872-64347873 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
28 | rs188823978 | chr13:64347876-64347877 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
29 | rs530954703 | chr13:64347877-64347878 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
30 | rs543027450 | chr13:64347881-64347882 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
31 | rs370821649 | chr13:64347882-64347883 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
32 | rs561232159 | chr13:64347902-64347903 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
33 | rs193221880 | chr13:64347904-64347905 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
34 | rs117384155 | chr13:64347995-64347996 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
35 | rs12866269 | chr13:64347996-64347997 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
36 | rs377206704 | chr13:64348007-64348008 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
37 | rs572525693 | chr13:64348076-64348077 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
38 | rs572029713 | chr13:64348084-64348085 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
39 | rs145182241 | chr13:64356163-64356164 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
40 | rs570476050 | chr13:64356182-64356183 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
41 | rs9539863 | chr13:64356201-64356202 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
42 | rs142171074 | chr13:64356202-64356203 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
43 | rs574603702 | chr13:64356265-64356266 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
44 | rs369716801 | chr13:64356273-64356274 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
45 | rs7985606 | chr13:64356296-64356297 | Inactive region | TF binding region | 1 gene(s) | LD-proxies of rSNPOverlapped rCNV | n/a |
46 | rs572393446 | chr13:64356318-64356319 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
47 | rs535794826 | chr13:64356366-64356367 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
48 | rs546078654 | chr13:64356392-64356393 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
49 | rs184630470 | chr13:64356417-64356418 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
50 | rs149598639 | chr13:64356424-64356425 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Esophageal squamous carcinoma | 21637470 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
HIV/AIDS | 22032296 | CNVD |
Prostate cancer | 16705090 | CNVD |
High-proliferative meningiomas | 17937814 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
Intellectual disability | 22102821 | CNVD |
Cancer | 20164919 | CNVD |
Autism | 22495311 | CNVD |
Chordoma | 21602918 | CNVD |
Bladder cancer | 21949216 | CNVD |
Acute myeloid leukemia | 16864856 | CNVD |
Burkitt''s lymphoma | 18698080 | CNVD |
Cancer | 21637783 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Chronic lymphocytic leukemia | 21518781 | CNVD |
colon cancer | 17210682 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Colorectal cancer | 20709793 | CNVD |
Astrocytoma | 17387387 | CNVD |
Breast cancer | 21264507 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Glioblastoma multiforme | 17387387 | CNVD |
Hepatocellular carcinoma | 22174799 | CNVD |
Ovarian cancer | 20844748 | CNVD |
Colorectal cancer | 19359472 | CNVD |
Intracranial aneurysm | 19064780 | CNVD |
Breast cancer | 19287154 | CNVD |
Acute myeloid leukemia | 18379011 | CNVD |
Human rectal carcinomas | 16397240 | CNVD |
Olfactory neuroblastoma | 18408657 | CNVD |
Multiple myeloma | 17077331 | CNVD |
Ependymoma | 16718352 | CNVD |
Oral squamous cell carcinoma | 17134496 | CNVD |
Colorectal cancer | 16272173 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Squamous cell cancer | 20885788 | CNVD |
Myeloproliferative neoplasm | 20015882 | CNVD |
Thyroid cancer | 19087340 | CNVD |
Gastrointestinal stromal cancer | 16982739 | CNVD |
Breast cancer | 16608533 | CNVD |
Neuroblastoma | 18923191 | CNVD |
Ovarian cancer | 22174824 | CNVD |
Breast cancer | 17133270 | CNVD |
Myoepithelioma | 18604193 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Acute lymphoblastic leukemia | 21098271 | CNVD |
Prostate cancer | 16573809 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
Paraganglioma | 21461997 | CNVD |
Pheochromocytoma | 21461997 | CNVD |
Acute lymphoblastic leukemia | 17690704 | CNVD |
Prostate cancer | 17245344 | CNVD |
Prostate cancer | 18632612 | CNVD |
Colorectal cancer | 21586687 | CNVD |
Small bowel adenocarcinoma | 21586687 | CNVD |
Retinoblastoma | 19183342 | CNVD |
Developmental delay | 21147756 | CNVD |
Melanoma | 18172304 | CNVD |
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Acute lymphoblastic leukemia | 22237106 | CNVD |
Merkel cell carcinoma | 19020549 | CNVD |
Basal cell lymphoma | 17053054 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Non-syndromic sensorineural hearing loss | 18496225 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Multiple myeloma | 17550852 | CNVD |
Breast cancer | 21858162 | CNVD |
Glioblastoma multiforme | 21922591 | CNVD |
Metanephric adenoma | 20802469 | CNVD |
High-grade prostatic intraepithelial neoplasia | 16573809 | CNVD |
Gastric cancer | 17908304 | CNVD |
Glioblastoma multiforme | 21750150 | CNVD |
Breast cancer | 17603634 | CNVD |
Cancer | 21183584 | CNVD |
Breast cancer | 17393978 | CNVD |
Splenic marginal zone lymphoma | 18492102 | CNVD |
Liposarcoma | 21253554 | CNVD |
Gastrointestinal stromal cancer | 20818650 | CNVD |
head and neck squamous cell carcinoma | 17671120 | CNVD |
Colorectal cancer | 16774939 | CNVD |
Adenoid cystic carcinoma | 17372589 | CNVD |
abnormal development | 18461090 | CNVD |
Acute promyelocytic leukemia | 19109227 | CNVD |
Chronic lymphocytic leukemia | 20421269 | CNVD |
Acute lymphoblastic leukemia | 21980252 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Lung cancer | 18438408 | CNVD |
Non-syndromic sensorineural hearing loss | 15273396 | CNVD |
Non-syndromic sensorineural hearing loss | 20606397 | CNVD |
early-passage human iPS cells | 21368824 | CNVD |
Non-syndromic sensorineural hearing loss | 22037309 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:64347400-64348200 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
2 | chr13:64384200-64386000 | Active TSS | HUES6 Cell Line | embryonic stem cell |
3 | chr13:64415000-64415200 | Enhancers | iPS DF 6.9 Cell Line | embryonic stem cell |
4 | chr13:64415000-64415600 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
5 | chr13:64415000-64415600 | ZNF genes & repeats | ES-UCSF4 Cell Line | embryonic stem cell |
6 | chr13:64415200-64415400 | ZNF genes & repeats | Foreskin Melanocyte Primary Cells skin01 | Skin |
7 | chr13:64415200-64415600 | ZNF genes & repeats | Foreskin Fibroblast Primary Cells skin02 | Skin |
8 | chr13:64415600-64418200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
9 | chr13:64415600-64419000 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
10 | chr13:64418200-64418600 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
11 | chr13:64418600-64420400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |