Variant report
| Variant | nsv515671 |
|---|---|
| Chromosome Location | chr8:127798574-127823662 |
| allele | n/a |
| Outlinks | Ensembl UCSC |
- TF binding region (count:252)
- CpG islands (count:61)
- Chromatin interactive region (count:11)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr8:127822176-127822226 | HRPEpiC | eye: | n/a |
| 2 | chr8:127822176-127822226 | AG09309 | skin: | n/a |
| 3 | chr8:127822176-127822226 | AG10803 | skin: | n/a |
| 4 | chr8:127822176-127822226 | BJ | skin: | n/a |
| 5 | chr8:127822176-127822226 | HepG2 | liver: | n/a |
| 6 | chr8:127822176-127822226 | T-47D | breast: | n/a |
| 7 | chr8:127822176-127822226 | BE2_C | brain: | n/a |
| 8 | chr8:127822176-127822226 | NT2-D1 | testis: | n/a |
| 9 | chr8:127822176-127822226 | ovcar-3 | ovarian: | n/a |
| 10 | chr8:127822176-127822226 | HAEpiC | amniotic membrane: | n/a |
| 11 | chr8:127822176-127822226 | CMK | blood: | n/a |
| 12 | chr8:127822176-127822226 | SK-N-SH | brain: | n/a |
| 13 | chr8:127822176-127822226 | HEEpiC | esophagus: | n/a |
| 14 | chr8:127822176-127822226 | ProgFib | skin: | n/a |
| 15 | chr8:127822176-127822226 | Hepatocyte | liver: | n/a |
| 16 | chr8:127822176-127822226 | NB4 | blood: | n/a |
| 17 | chr8:127822176-127822226 | LNCaP | prostate: | n/a |
| 18 | chr8:127822176-127822226 | SK-N-SH_RA | brain: | n/a |
| 19 | chr8:127822176-127822226 | AG04450 | lung: | fetal |
| 20 | chr8:127822176-127822226 | U87 | brain: | n/a |
| 21 | chr8:127822176-127822226 | MCF10A-Er-Src | breast: | n/a |
| 22 | chr8:127822176-127822226 | GM12878 | blood: | n/a |
| 23 | chr8:127822176-127822226 | RPTEC | kidney: | n/a |
| 24 | chr8:127822176-127822226 | HCM | heart: | n/a |
| 25 | chr8:127822176-127822226 | SK-N-MC | brain: | n/a |
| 26 | chr8:127822176-127822226 | HIPEpiC | eye: | n/a |
| 27 | chr8:127822176-127822226 | GM19239 | blood: | n/a |
| 28 | chr8:127822176-127822226 | K562 | blood: | n/a |
| 29 | chr8:127822176-127822226 | IMR90 | lung: | fetal |
| 30 | chr8:127822176-127822226 | NHBE | bronchial: | n/a |
| 31 | chr8:127822176-127822226 | PFSK-1 | brain: | n/a |
| 32 | chr8:127822176-127822226 | HRE | kidney: | n/a |
| 33 | chr8:127822176-127822226 | GM06990 | blood: | n/a |
| 34 | chr8:127822176-127822226 | H1-hESC | embryonic stem cell: | embryo |
| 35 | chr8:127822176-127822226 | GM12892 | blood: | n/a |
| 36 | chr8:127822176-127822226 | GM12891 | blood: | n/a |
| 37 | chr8:127822176-127822226 | HRCEpiC | kidney: | n/a |
| 38 | chr8:127822176-127822226 | HUVEC | blood vessel: | n/a |
| 39 | chr8:127822176-127822226 | SAEC | small airway: | n/a |
| 40 | chr8:127822176-127822226 | AG09319 | gingival: | n/a |
| 41 | chr8:127822176-127822226 | Hela-S3 | cervix: | n/a |
| 42 | chr8:127822176-127822226 | ECC-1 | luminal epithelium: | n/a |
| 43 | chr8:127822176-127822226 | HCPEpiC | choroid plexus: | n/a |
| 44 | chr8:127822176-127822226 | A549 | lung: | n/a |
| 45 | chr8:127822176-127822226 | HMEC | breast: | n/a |
| 46 | chr8:127822176-127822226 | AoSMC | blood vessel: | n/a |
| 47 | chr8:127822176-127822226 | HPAEpiC | pulmonary alveolar: | n/a |
| 48 | chr8:127822176-127822226 | PANC-1 | pancreas: | n/a |
| 49 | chr8:127822176-127822226 | HCT-116 | colon: | n/a |
| 50 | chr8:127822176-127822226 | AG04449 | skin: | fetal |
(count:11 , 50 per page) page:
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| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr8:127805192..127807275-chr8:127809122..127812118,2 | MCF-7 | breast: | |
| 2 | chr8:127805192..127807275-chr8:127809122..127812118,2 | MCF-7 | breast: | |
| 3 | chr8:127798629..127800610-chr8:127804346..127806668,2 | K562 | blood: | |
| 4 | chr8:127522237..127522942-chr8:127821828..127822807,3 | MCF-7 | breast: | |
| 5 | chr8:127562999..127565215-chr8:127820226..127822358,2 | MCF-7 | breast: | |
| 6 | chr8:126969649..126970327-chr8:127821699..127822564,2 | MCF-7 | breast: | |
| 7 | chr8:127615907..127617116-chr8:127821861..127822821,4 | K562 | blood: | |
| 8 | chr8:127798629..127800610-chr8:127804346..127806668,2 | K562 | blood: | |
| 9 | chr8:127808316..127811261-chr8:132840398..132845431,4 | MCF-7 | breast: | |
| 10 | chr8:127569143..127571492-chr8:127820912..127823847,3 | MCF-7 | breast: | |
| 11 | chr8:127570025..127572998-chr8:127803359..127806177,2 | MCF-7 | breast: |
(count:1 , 50 per page) page:
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| No. | lncRNA name | Chromosome Location | lncRNA alias |
|---|---|---|---|
| 1 | lnc-FAM84B-3 | chr8:127802813-127802882 | ENSG00000253573 |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000253573 | TF binding region |
| ENSG00000253573 | CpG island |
| ENSG00000254286 | chromatin interactions |
| ENSG00000168672 | chromatin interactions |
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs189045549 | chr8:127802815-127802816 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 2 | rs556699659 | chr8:127802826-127802827 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
| 3 | rs545299003 | chr8:127803224-127803225 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
| 4 | rs565460435 | chr8:127803229-127803230 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
| 5 | rs528015311 | chr8:127803274-127803275 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
| 6 | rs548106824 | chr8:127803283-127803284 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
| 7 | rs567912326 | chr8:127803379-127803380 | ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 8 | rs143238280 | chr8:127803400-127803401 | ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 9 | rs79519490 | chr8:127803424-127803425 | ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 10 | rs183087536 | chr8:127803426-127803427 | ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 11 | rs148759446 | chr8:127803434-127803435 | ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 12 | rs549254588 | chr8:127803533-127803534 | ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 13 | rs565859576 | chr8:127803540-127803541 | ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 14 | rs187414851 | chr8:127803597-127803598 | ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 15 | rs554449735 | chr8:127803619-127803620 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 16 | rs112311204 | chr8:127803629-127803630 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 17 | rs191789174 | chr8:127803635-127803636 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 18 | rs375939739 | chr8:127803667-127803668 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 19 | rs183999400 | chr8:127803695-127803696 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 20 | rs556893431 | chr8:127803711-127803712 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 21 | rs576898060 | chr8:127803744-127803745 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 22 | rs561235352 | chr8:127803795-127803796 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 23 | rs187732186 | chr8:127803804-127803805 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 24 | rs118079201 | chr8:127803857-127803858 | Weak transcription | TF binding regionChromatin interactive region | 3 gene(s) | Overlapped CNVs | n/a |
| 25 | rs565384391 | chr8:127803906-127803907 | Weak transcription | TF binding regionChromatin interactive region | 3 gene(s) | Overlapped CNVs | n/a |
| 26 | rs192702465 | chr8:127803961-127803962 | Weak transcription | TF binding regionChromatin interactive region | 3 gene(s) | Overlapped CNVs | n/a |
| 27 | rs142399273 | chr8:127803977-127803978 | Weak transcription | TF binding regionChromatin interactive region | 3 gene(s) | Overlapped CNVs | n/a |
| 28 | rs561585164 | chr8:127803985-127803986 | Weak transcription | TF binding regionChromatin interactive region | 3 gene(s) | Overlapped CNVs | n/a |
| 29 | rs35666938 | chr8:127804001-127804002 | Weak transcription | TF binding regionChromatin interactive region | 3 gene(s) | Overlapped CNVs | n/a |
| 30 | rs185655567 | chr8:127804087-127804088 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 31 | rs550228503 | chr8:127804088-127804089 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 32 | rs112940388 | chr8:127804111-127804112 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 33 | rs532540742 | chr8:127804115-127804116 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 34 | rs528117030 | chr8:127804128-127804129 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 35 | rs565997212 | chr8:127804164-127804165 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 36 | rs534521936 | chr8:127804169-127804170 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 37 | rs547950977 | chr8:127804174-127804175 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 38 | rs546561526 | chr8:127804199-127804200 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 39 | rs568041258 | chr8:127804213-127804214 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 40 | rs75924973 | chr8:127804234-127804235 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 41 | rs190584109 | chr8:127804240-127804241 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 42 | rs114822374 | chr8:127804253-127804254 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 43 | rs539016772 | chr8:127804259-127804260 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 44 | rs184417975 | chr8:127804270-127804271 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 45 | rs188763764 | chr8:127804288-127804289 | Weak transcription | Chromatin interactive region | 2 gene(s) | Overlapped CNVs | n/a |
| 46 | rs140591459 | chr8:127804297-127804298 | Weak transcription | TF binding regionChromatin interactive region | 3 gene(s) | Overlapped CNVs | n/a |
| 47 | rs541668239 | chr8:127804307-127804308 | Weak transcription | TF binding regionChromatin interactive region | 3 gene(s) | Overlapped CNVs | n/a |
| 48 | rs561447432 | chr8:127804312-127804313 | Weak transcription | TF binding regionChromatin interactive region | 3 gene(s) | Overlapped CNVs | n/a |
| 49 | rs147044781 | chr8:127804315-127804316 | Weak transcription | TF binding regionChromatin interactive region | 3 gene(s) | Overlapped CNVs | n/a |
| 50 | rs575245814 | chr8:127804342-127804343 | Weak transcription | TF binding regionChromatin interactive region | 3 gene(s) | Overlapped CNVs | n/a |
Variant related diseases (count:156)
| Disease | PMID | Source |
|---|---|---|
| Medulloblastoma | 21979893 | CNVD |
| Ewing''s sarcoma | 21437220 | CNVD |
| Autism | 19415332 | CNVD |
| Malaria | 21533027 | CNVD |
| Non-syndromic sensorineural hearing loss | 22037309 | CNVD |
| Esophageal cancer | 21851588 | CNVD |
| Gastric cancer | 17908304 | CNVD |
| Acute promyelocytic leukemia | 19109227 | CNVD |
| Breast cancer | 21245420 | CNVD |
| T-cell prolymphocytic leukemia | 19278963 | CNVD |
| Liver carcinoma | 19366792 | CNVD |
| Seminomas | 18059402 | CNVD |
| Acute lymphoblastic leukemia | 21390130 | CNVD |
| Pancreatic cancer | 21811587 | CNVD |
| Thyroid cancer | 19087340 | CNVD |
| Myelofibrosis | 22110671 | CNVD |
| Testicular cancer | 18059402 | CNVD |
| Breast cancer | 17133270 | CNVD |
| Breast cancer | 21509527 | CNVD |
| Breast cancer | 21858162 | CNVD |
| Acute lymphoblastic leukemia | 20435627 | CNVD |
| Acute lymphoblastic leukemia | 21248843 | CNVD |
| abnormal development | 18461090 | CNVD |
| Oral cancer | 21386901 | CNVD |
| Uveal melanoma | 21693616 | CNVD |
| Langer-Giedion syndrome | 22283845 | CNVD |
| Cancer | 21637783 | CNVD |
| Splenic marginal zone lymphoma | 21957467 | CNVD |
| Breast cancer | 20632083 | CNVD |
| Breast cancer | 17603634 | CNVD |
| Breast cancer | 19602461 | CNVD |
| Cancer | 22429812 | CNVD |
| Endometrial cancer | 22040021 | CNVD |
| Esophageal squamous carcinoma | 21637470 | CNVD |
| Glioblastoma multiforme | 19960244 | CNVD |
| Glioblastoma multiforme | 21080181 | CNVD |
| Hepatocellular carcinoma | 22174799 | CNVD |
| Oral cancer | 19627613 | CNVD |
| Prostate cancer | 21088497 | CNVD |
| colon cancer | 17210682 | CNVD |
| Breast cancer | 21264507 | CNVD |
| Breast cancer | 22028636 | CNVD |
| Acute myeloid leukemia | 16864856 | CNVD |
| Cancer | 16751803 | CNVD |
| Esophageal squamous carcinoma | 18350619 | CNVD |
| Gastric cancer | 17167181 | CNVD |
| Colorectal cancer | 19359472 | CNVD |
| Breast cancer | 16461572 | CNVD |
| Human rectal carcinomas | 16397240 | CNVD |
| Medulloblastoma | 16968546 | CNVD |
| head and neck squamous cell carcinoma | 18028549 | CNVD |
| Breast cancer | 17001317 | CNVD |
| Chronic lymphocytic leukemia | 21546498 | CNVD |
| Acute myeloid leukemia | 20729466 | CNVD |
| Ewing''s sarcoma | 17952124 | CNVD |
| Urothelial carcinoma | 21177765 | CNVD |
| Lung cancer | 18438408 | CNVD |
| Breast cancer | 16608533 | CNVD |
| Metanephric adenoma | 20802469 | CNVD |
| Hepatocellular carcinoma | 18803288 | CNVD |
| Prostate cancer | 18632612 | CNVD |
| Ovarian cancer | 22174824 | CNVD |
| Prostate cancer | 16573809 | CNVD |
| Malignant peripheral nerve sheath tumor | 18522746 | CNVD |
| Adenocarcinoma | 21044232 | CNVD |
| Squamous cell cancer | 20885788 | CNVD |
| T-cell prolymphocytic leukemia | 17713554 | CNVD |
| Prostate cancer | 16461572 | CNVD |
| Breast cancer | 21399628 | CNVD |
| High-grade prostatic intraepithelial neoplasia | 16573809 | CNVD |
| Acute lymphoblastic leukemia | 17690704 | CNVD |
| Breast cancer | 17393978 | CNVD |
| Burkitt''s lymphoma | 18698080 | CNVD |
| Non-syndromic sensorineural hearing loss | 20606397 | CNVD |
| Breast cancer | 17899364 | CNVD |
| Acute myeloid leukemia | 21251322 | CNVD |
| lymphocytic leukemia | 21291569 | CNVD |
| Endometrioid adenocarcinoma | 16974079 | CNVD |
| Developmental delay | 21147756 | CNVD |
| Hodgkin''s lymphoma | 17606441 | CNVD |
| Congenital diaphragmatic hernia | 21525063 | CNVD |
| Non-small cell lung cancer | 19010865 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| Papillary thyroid cancer | 17515504 | CNVD |
| Basal cell lymphoma | 17053054 | CNVD |
| Breast cancer | 20932292 | CNVD |
| Gastric cancer | 21528007 | CNVD |
| Breast cancer | 22532251 | CNVD |
| Cervical cancer | 21062161 | CNVD |
| Cancer | 21129771 | CNVD |
| benign familial neonatal convulsions | 18472482 | CNVD |
| Breast cancer | 16417655 | CNVD |
| Astrocytoma | 17387387 | CNVD |
| Cancer | 21183584 | CNVD |
| Follicular lymphoma | 20505157 | CNVD |
| T-cell lymphomas | 19863542 | CNVD |
| Colorectal cancer | 20709793 | CNVD |
| Medulloblastoma | 20607354 | CNVD |
| Breast cancer | 20814816 | CNVD |
| Colorectal cancer | 22486879 | CNVD |
| Breast cancer | 17908964 | CNVD |
| Colorectal cancer | 20031965 | CNVD |
| Hepatocellular carcinoma | 16750200 | CNVD |
| Ovarian cancer | 17908964 | CNVD |
| Ovarian cancer | 20031965 | CNVD |
| Prostate cancer | 20031965 | CNVD |
| Non-small cell lung cancer | 17643093 | CNVD |
| Prostate cancer | 19242612 | CNVD |
| Colorectal cancer | 16774939 | CNVD |
| Glioblastoma multiforme | 18628472 | CNVD |
| Malignant melanoma | 17260012 | CNVD |
| Diffuse large b-cell lymphoma | 18287131 | CNVD |
| Breast cancer | 21364760 | CNVD |
| Burkitt''s lymphoma | 20823134 | CNVD |
| Acute myeloid leukemia | 17268525 | CNVD |
| Acute myeloid leukemia | 18379011 | CNVD |
| Esophageal squamous carcinoma | 18405350 | CNVD |
| Chronic lymphocytic leukemia | 20421269 | CNVD |
| Ductal carcinoma | 22052326 | CNVD |
| Gastric cancer | 18160780 | CNVD |
| Gastric cancer | 21635755 | CNVD |
| low-grade B-cell lymphoma tumor | 18367492 | CNVD |
| Acute lymphoblastic leukemia | 21339820 | CNVD |
| Sezary syndrome | 18413736 | CNVD |
| Breast cancer | 21611746 | CNVD |
| Breast cancer | 22048815 | CNVD |
| Colorectal cancer | 16912164 | CNVD |
| Cutaneous T-cell lymphoma | 21881587 | CNVD |
| Lung adenocarcinoma | 21148746 | CNVD |
| Lung cancer | 21911935 | CNVD |
| Breast cancer | 20459607 | CNVD |
| Medulloblastoma | 19270706 | CNVD |
| Acute myeloid leukemia | 19651601 | CNVD |
| Colorectal cancer | 21645411 | CNVD |
| Congenital anomalies of the kidney and urinary tract | 18316590 | CNVD |
| Colorectal cancer | 19455253 | CNVD |
| Glioblastoma multiforme | 22286061 | CNVD |
| Colorectal cancer | 22860045 | CNVD |
| Esophageal squamous carcinoma | 17470683 | CNVD |
| Lung cancer | 17925434 | CNVD |
| Non-small cell lung cancer | 21829676 | CNVD |
| Prostate cancer | 17217626 | CNVD |
| Cancer | 17160897 | CNVD |
| Breast cancer | 16497871 | CNVD |
| Colorectal cancer | 16882699 | CNVD |
| Cystic fibrosis | 19273617 | CNVD |
| Chronic stroke | 19622162 | CNVD |
| Chordoma | 18071362 | CNVD |
| Breast cancer | 17850661 | CNVD |
| head and neck squamous cell carcinoma | 16740747 | CNVD |
| Gastric cancer | 22539939 | CNVD |
| Breast cancer | 16272173 | CNVD |
| Uveal melanoma | 20484589 | CNVD |
| Ovarian cancer | 20844748 | CNVD |
| Multiple myeloma | 16616336 | CNVD |
| Breast cancer | 16620391 | CNVD |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr8:127803200-127803600 | ZNF genes & repeats | Pancreas | Pancrea |
| 2 | chr8:127803600-127808600 | Weak transcription | Pancreas | Pancrea |
| 3 | chr8:127805600-127806000 | Weak transcription | Primary T regulatory cells fromperipheralblood | blood |
| 4 | chr8:127806400-127806800 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |
| 5 | chr8:127808000-127808800 | Enhancers | HMEC | breast |
| 6 | chr8:127808200-127808800 | Enhancers | Stomach Mucosa | stomach |
| 7 | chr8:127808200-127809000 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 8 | chr8:127808200-127809000 | Enhancers | NHEK | skin |
| 9 | chr8:127811600-127812000 | Enhancers | K562 | blood |
| 10 | chr8:127817200-127818000 | Active TSS | ES-I3 Cell Line | embryonic stem cell |
| 11 | chr8:127817200-127818200 | Active TSS | HUES6 Cell Line | embryonic stem cell |
| 12 | chr8:127817400-127817800 | Active TSS | H9 Cell Line | embryonic stem cell |
| 13 | chr8:127817400-127817800 | Active TSS | iPS-18 Cell Line | embryonic stem cell |
| 14 | chr8:127817400-127817800 | Active TSS | iPS DF 19.11 Cell Line | embryonic stem cell |
| 15 | chr8:127817400-127818000 | Active TSS | iPS-15b Cell Line | embryonic stem cell |
| 16 | chr8:127817400-127818200 | Active TSS | ES-WA7 Cell Line | embryonic stem cell |
| 17 | chr8:127817400-127818200 | Active TSS | K562 | blood |
| 18 | chr8:127817800-127821800 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
| 19 | chr8:127818200-127822000 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
| 20 | chr8:127821200-127821800 | Enhancers | Fetal Brain Male | brain |
| 21 | chr8:127821600-127822600 | Enhancers | HUES64 Cell Line | embryonic stem cell |
| 22 | chr8:127821800-127822200 | Enhancers | ES-WA7 Cell Line | embryonic stem cell |
| 23 | chr8:127821800-127822200 | Weak transcription | Fetal Brain Male | brain |
| 24 | chr8:127821800-127822600 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
| 25 | chr8:127822000-127822600 | Enhancers | HUES6 Cell Line | embryonic stem cell |
| 26 | chr8:127822000-127822600 | Enhancers | Cortex derived primary cultured neurospheres | brain |
| 27 | chr8:127822000-127822800 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
| 28 | chr8:127822200-127822600 | Enhancers | Primary T helper cells fromperipheralblood | blood |
| 29 | chr8:127822200-127822800 | Enhancers | Fetal Brain Male | brain |
| 30 | chr8:127822400-127822600 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
| 31 | chr8:127822800-127823600 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
| 32 | chr8:127823600-127824000 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
