Variant report
| Variant | nsv549464 |
|---|---|
| Chromosome Location | chr1:242411114-242842300 |
| allele | n/a |
| Outlinks | Ensembl   UCSC |
- TF binding region (count:1861)
- CpG islands (count:1589)
- Chromatin interactive region (count:41)
- LncRNA region (count:12)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr1:242688523-242688573 | T-47D | breast: | n/a |
| 2 | chr1:242749065-242749115 | NT2-D1 | testis: | n/a |
| 3 | chr1:242612787-242612837 | HCT-116 | colon: | n/a |
| 4 | chr1:242688523-242688573 | T-47D | breast: | n/a |
| 5 | chr1:242749065-242749115 | NT2-D1 | testis: | n/a |
| 6 | chr1:242612787-242612837 | HCT-116 | colon: | n/a |
| 7 | chr1:242683142-242683192 | PrEC | prostate: | n/a |
| 8 | chr1:242688591-242688641 | ECC-1 | luminal epithelium: | n/a |
| 9 | chr1:242688226-242688276 | NB4 | blood: | n/a |
| 10 | chr1:242611826-242611876 | HMEC | breast: | n/a |
| 11 | chr1:242613203-242613253 | HPAEpiC | pulmonary alveolar: | n/a |
| 12 | chr1:242688591-242688641 | Jurkat | blood: | n/a |
| 13 | chr1:242688591-242688641 | HEK293 | kidney: | embryo |
| 14 | chr1:242687018-242687068 | HNPCEpiC | eye: | n/a |
| 15 | chr1:242613245-242613295 | T-47D | breast: | n/a |
| 16 | chr1:242653362-242653412 | HEK293 | kidney: | embryo |
| 17 | chr1:242688320-242688370 | AoSMC | blood vessel: | n/a |
| 18 | chr1:242687527-242687577 | MCF-7 | breast: | n/a |
| 19 | chr1:242749065-242749115 | BJ | skin: | n/a |
| 20 | chr1:242687018-242687068 | HEK293 | kidney: | embryo |
| 21 | chr1:242684042-242684092 | Jurkat | blood: | n/a |
| 22 | chr1:242612787-242612837 | PrEC | prostate: | n/a |
| 23 | chr1:242688591-242688641 | SK-N-SH | brain: | n/a |
| 24 | chr1:242767727-242767777 | HCM | heart: | n/a |
| 25 | chr1:242688523-242688573 | U87 | brain: | n/a |
| 26 | chr1:242613203-242613253 | HL-60 | blood: | n/a |
| 27 | chr1:242653362-242653412 | BE2_C | brain: | n/a |
| 28 | chr1:242690593-242690643 | AG09319 | gingival: | n/a |
| 29 | chr1:242687465-242687515 | HEK293 | kidney: | embryo |
| 30 | chr1:242688523-242688573 | HAEpiC | amniotic membrane: | n/a |
| 31 | chr1:242688681-242688731 | PrEC | prostate: | n/a |
| 32 | chr1:242605061-242605111 | HNPCEpiC | eye: | n/a |
| 33 | chr1:242687412-242687462 | HEEpiC | esophagus: | n/a |
| 34 | chr1:242686709-242686759 | SKMC | muscle: | n/a |
| 35 | chr1:242611826-242611876 | IMR90 | lung: | fetal |
| 36 | chr1:242690593-242690643 | ECC-1 | luminal epithelium: | n/a |
| 37 | chr1:242687412-242687462 | AG10803 | skin: | n/a |
| 38 | chr1:242767942-242767992 | MCF-7 | breast: | n/a |
| 39 | chr1:242688681-242688731 | HCF | heart: | n/a |
| 40 | chr1:242686709-242686759 | T-47D | breast: | n/a |
| 41 | chr1:242684042-242684092 | T-47D | breast: | n/a |
| 42 | chr1:242613245-242613295 | HMEC | breast: | n/a |
| 43 | chr1:242767942-242767992 | U87 | brain: | n/a |
| 44 | chr1:242690733-242690783 | HRCEpiC | kidney: | n/a |
| 45 | chr1:242686709-242686759 | HL-60 | blood: | n/a |
| 46 | chr1:242686709-242686759 | H1-hESC | embryonic stem cell: | embryo |
| 47 | chr1:242687412-242687462 | K562 | blood: | n/a |
| 48 | chr1:242611826-242611876 | GM06990 | blood: | n/a |
| 49 | chr1:242684042-242684092 | Hela-S3 | cervix: | n/a |
| 50 | chr1:242684042-242684092 | ProgFib | skin: | n/a |
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| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr1:242594168..242597872-chr1:242601027..242602906,3 | K562 | blood: | |
| 2 | chr1:242630619..242631512-chr1:244436093..244436950,3 | MCF-7 | breast: | |
| 3 | chr1:242687782..242688282-chr7:140396130..140396992,2 | MCF-7 | breast: | |
| 4 | chr1:242731452..242733233-chr1:242737501..242739906,2 | K562 | blood: | |
| 5 | chr1:242590294..242592687-chr1:242593690..242595305,2 | K562 | blood: | |
| 6 | chr1:242595107..242597872-chr1:242601027..242602558,2 | K562 | blood: | |
| 7 | chr1:242690016..242691872-chr1:242693633..242696620,2 | K562 | blood: | |
| 8 | chr1:242292163..242292685-chr1:242427746..242428399,2 | MCF-7 | breast: | |
| 9 | chr1:242183008..242183632-chr1:242588513..242589035,2 | MCF-7 | breast: | |
| 10 | chr1:242617811..242618559-chr1:242630673..242631426,2 | MCF-7 | breast: | |
| 11 | chr1:242579229..242580899-chr1:242592362..242595019,2 | K562 | blood: | |
| 12 | chr1:242616929..242619643-chr1:242629672..242631653,2 | K562 | blood: | |
| 13 | chr1:242817323..242819787-chr1:242897350..242900264,2 | K562 | blood: | |
| 14 | chr1:242590294..242592687-chr1:242593690..242595305,2 | K562 | blood: | |
| 15 | chr1:242608265..242609787-chr20:56286531..56288293,2 | MCF-7 | breast: | |
| 16 | chr1:242617851..242618670-chr1:243488347..243489044,3 | K562 | blood: | |
| 17 | chr1:242616929..242619643-chr1:242629672..242631653,2 | K562 | blood: | |
| 18 | chr1:242687074..242690257-chr1:242691020..242695095,4 | K562 | blood: | |
| 19 | chr1:242570206..242572074-chr1:242586277..242589124,2 | K562 | blood: | |
| 20 | chr1:242725284..242727359-chr1:242740097..242742633,2 | K562 | blood: | |
| 21 | chr1:242182892..242183793-chr1:242638283..242638859,2 | MCF-7 | breast: | |
| 22 | chr1:242692263..242693064-chr17:56708576..56709248,2 | MCF-7 | breast: | |
| 23 | chr1:242626775..242629510-chr1:242632318..242634678,2 | K562 | blood: | |
| 24 | chr1:242579229..242580899-chr1:242592362..242595019,2 | K562 | blood: | |
| 25 | chr1:242690016..242691872-chr1:242693633..242696620,2 | K562 | blood: | |
| 26 | chr1:242725284..242727359-chr1:242740097..242742633,2 | K562 | blood: | |
| 27 | chr1:242570206..242572074-chr1:242586277..242589124,2 | K562 | blood: | |
| 28 | chr1:242617838..242618342-chr1:242955947..242956813,2 | MCF-7 | breast: | |
| 29 | chr1:242617811..242618559-chr1:242630673..242631426,2 | MCF-7 | breast: | |
| 30 | chr1:242626775..242629510-chr1:242632318..242634678,2 | K562 | blood: | |
| 31 | chr1:242594168..242597872-chr1:242601027..242602906,3 | K562 | blood: | |
| 32 | chr1:242595107..242597872-chr1:242601027..242602558,2 | K562 | blood: | |
| 33 | chr1:242532755..242535089-chr1:242538620..242540939,2 | MCF-7 | breast: | |
| 34 | chr1:242731452..242733233-chr1:242737501..242739906,2 | K562 | blood: | |
| 35 | chr1:242536607..242538996-chr1:242545702..242547462,2 | MCF-7 | breast: | |
| 36 | chr1:242595852..242597675-chr1:242599631..242602192,2 | MCF-7 | breast: | |
| 37 | chr1:242687461..242689938-chr1:242691020..242693615,2 | K562 | blood: | |
| 38 | chr1:242576728..242577460-chr2:3592302..3593192,2 | MCF-7 | breast: | |
| 39 | chr1:242536607..242538996-chr1:242545702..242547462,2 | MCF-7 | breast: | |
| 40 | chr1:242680127..242681627-chr2:114917951..114919998,2 | K562 | blood: | |
| 41 | chr1:242595852..242597675-chr1:242599631..242602192,2 | MCF-7 | breast: |
(count:12 , 50 per page) page:
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| No. | lncRNA name | Chromosome Location | lncRNA alias |
|---|---|---|---|
| 1 | lnc-MAP1LC3C-3 | chr1:242654490-242654577 | NONHSAT010568 |
| 2 | lnc-PLD5-1 | chr1:242690923-242691021 | NONHSAT010569 |
| 3 | lnc-SDCCAG8-4 | chr1:242834442-242834878 | NONHSAT010573 |
| 4 | lnc-MAP1LC3C-4 | chr1:242654836-242655140 | expReg_chr1_22645_- |
| 5 | lnc-PLD5-2 | chr1:242717724-242718022 | XLOC_001281 |
| 6 | lnc-MAP1LC3C-5 | chr1:242676012-242676332 | expReg_chr1_22653_- |
| 7 | lnc-PLD5-2 | chr1:242717038-242717147 | XLOC_001281 |
| 8 | lnc-MAP1LC3C-7 | chr1:242681118-242681325 | expReg_chr1_22661_- |
| 9 | lnc-MAP1LC3C-6 | chr1:242680432-242680918 | expReg_chr1_22659_- |
| 10 | lnc-PLD5-1 | chr1:242693049-242693341 | NONHSAT010569 |
| 11 | lnc-MAP1LC3C-3 | chr1:242652877-242653660 | NONHSAT010568 |
| 12 | lnc-PLD5-1 | chr1:242692647-242692740 | NONHSAT010569 |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000270859 | TF binding region |
| ENSG00000235467 | TF binding region |
| PLD5 | TF binding region |
| ENSG00000213690 | TF binding region |
| ENSG00000226750 | TF binding region |
| ENSG00000270859 | CpG island |
| ENSG00000235467 | CpG island |
| PLD5 | CpG island |
| ENSG00000213690 | CpG island |
| ENSG00000226750 | CpG island |
| ENSG00000180287 | chromatin interactions |
| ENSG00000240889 | chromatin interactions |
| ENSG00000090266 | chromatin interactions |
| ENSG00000213690 | chromatin interactions |
| ENSG00000124225 | chromatin interactions |
| ENSG00000212195 | chromatin interactions |
| DAB2IP | miRNA target sites |
| DACT1 | miRNA target sites |
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs316901 | chr1:242411114-242411115 | Weak transcription Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | mRNA abundance |
| 2 | rs565710662 | chr1:242411132-242411133 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 3 | rs557286203 | chr1:242411146-242411147 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 4 | rs184883435 | chr1:242411187-242411188 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 5 | rs531232792 | chr1:242411228-242411229 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 6 | rs551253156 | chr1:242411236-242411237 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 7 | rs149166807 | chr1:242411305-242411306 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 8 | rs536827177 | chr1:242411306-242411307 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 9 | rs553268891 | chr1:242411349-242411350 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 10 | rs189755295 | chr1:242411426-242411427 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 11 | rs181404769 | chr1:242411471-242411472 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 12 | rs115576468 | chr1:242411508-242411509 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 13 | rs3001661 | chr1:242411519-242411520 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 14 | rs557334541 | chr1:242411538-242411539 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 15 | rs577177762 | chr1:242411543-242411544 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 16 | rs74450980 | chr1:242411581-242411582 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 17 | rs367834542 | chr1:242411589-242411590 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 18 | rs370365740 | chr1:242411603-242411604 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 19 | rs543329875 | chr1:242411608-242411609 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 20 | rs556811127 | chr1:242411654-242411655 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 21 | rs372188038 | chr1:242411676-242411677 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 22 | rs316900 | chr1:242411685-242411686 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 23 | rs542844451 | chr1:242411686-242411687 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 24 | rs61845480 | chr1:242411716-242411717 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 25 | rs559277015 | chr1:242411742-242411743 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 26 | rs3001662 | chr1:242411744-242411745 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 27 | rs528629102 | chr1:242411748-242411749 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 28 | rs55896046 | chr1:242411784-242411785 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 29 | rs78029206 | chr1:242411793-242411794 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 30 | rs199739509 | chr1:242411795-242411796 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 31 | rs545122934 | chr1:242411811-242411812 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 32 | rs148355824 | chr1:242411815-242411816 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 33 | rs530890296 | chr1:242411816-242411817 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 34 | rs186548474 | chr1:242411818-242411819 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 35 | rs2917447 | chr1:242411836-242411837 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 36 | rs567987482 | chr1:242411848-242411849 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 37 | rs2917446 | chr1:242411870-242411871 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 38 | rs56328111 | chr1:242411873-242411874 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 39 | rs112975289 | chr1:242411887-242411888 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 40 | rs138595715 | chr1:242412052-242412053 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 41 | rs12726773 | chr1:242412060-242412061 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 42 | rs557398235 | chr1:242412086-242412087 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 43 | rs570933340 | chr1:242412092-242412093 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 44 | rs316899 | chr1:242412136-242412137 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 45 | rs71498891 | chr1:242412173-242412174 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 46 | rs556525908 | chr1:242412198-242412199 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 47 | rs573921430 | chr1:242412201-242412202 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 48 | rs542552444 | chr1:242412204-242412205 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 49 | rs139445479 | chr1:242412206-242412207 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 50 | rs572908668 | chr1:242412219-242412220 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| Disease | PMID | Source |
|---|---|---|
| Esophageal squamous carcinoma | 21637470 | CNVD |
| HIV/AIDS | 22032296 | CNVD |
| Schizophrenia | 19415332 | CNVD |
| Melanoma | 18172304 | CNVD |
| Rett syndrome | 21593744 | CNVD |
| Medulloblastoma | 21979893 | CNVD |
| Cancer | 20164919 | CNVD |
| Wilms tumour | 21544195 | CNVD |
| Breast cancer | 17133270 | CNVD |
| Non-small cell lung cancer | 21044232 | CNVD |
| Cervical cancer | 21063398 | CNVD |
| Acute lymphoblastic leukemia | 20435627 | CNVD |
| Astrocytoma | 17387387 | CNVD |
| Breast cancer | 20632083 | CNVD |
| Endometrial cancer | 22040021 | CNVD |
| Ewing''s sarcoma | 21437220 | CNVD |
| Gastrointestinal stromal cancer | 20470368 | CNVD |
| Glioblastoma multiforme | 19960244 | CNVD |
| Glioblastoma multiforme | 21080181 | CNVD |
| Hepatocellular carcinoma | 22174799 | CNVD |
| Medulloblastoma | 21292688 | CNVD |
| Phyllodes tumor | 17334353 | CNVD |
| Breast cancer | 21264507 | CNVD |
| Liposarcoma | 21253554 | CNVD |
| Multiple myeloma | 21628407 | CNVD |
| Cancer | 16751803 | CNVD |
| Prostate cancer | 16705090 | CNVD |
| Neuroblastoma | 19435921 | CNVD |
| Breast cancer | 17850661 | CNVD |
| Breast cancer | 16461572 | CNVD |
| Intracranial tumor | 16823260 | CNVD |
| Medulloblastoma | 18056178 | CNVD |
| Monoclonal gammopathy of undetermined significance | 17077331 | CNVD |
| Primary mediastinal b-cell lymphoma | 17728785 | CNVD |
| Colorectal cancer | 16272173 | CNVD |
| Neuroblastoma | 21899760 | CNVD |
| Breast cancer | 21858162 | CNVD |
| Acute lymphoblastic leukemia | 21980252 | CNVD |
| Breast cancer | 16608533 | CNVD |
| Ewing''s sarcoma | 22429812 | CNVD |
| Acute promyelocytic leukemia | 19109227 | CNVD |
| Basal cell lymphoma | 16317097 | CNVD |
| Diffuse large b-cell lymphoma | 16317097 | CNVD |
| Breast cancer | 17001317 | CNVD |
| Acute myeloid leukemia | 21251322 | CNVD |
| Multiple myeloma | 17550852 | CNVD |
| Acute myeloid leukemia | 20729466 | CNVD |
| Hodgkin''s lymphoma | 17606441 | CNVD |
| Testicular germ cell tumor | 18059402 | CNVD |
| Ependymoma | 18628472 | CNVD |
| Leukemia | 18628472 | CNVD |
| Neuroblastoma | 18923191 | CNVD |
| Acute lymphoblastic leukemia | 19100363 | CNVD |
| Breast cancer | 21509527 | CNVD |
| Urothelial carcinoma | 21177765 | CNVD |
| Acute lymphoblastic leukemia | 20067559 | CNVD |
| Chordoma | 18071362 | CNVD |
| T-cell prolymphocytic leukemia | 19278963 | CNVD |
| Hepatocellular carcinoma | 18803288 | CNVD |
| Urothelial tumor | 18831757 | CNVD |
| Lung cancer | 18438408 | CNVD |
| Medulloblastoma | 16783165 | CNVD |
| Basal cell lymphoma | 17170743 | CNVD |
| Basal cell lymphoma | 17053054 | CNVD |
| Chronic lymphocytic leukemia | 21546498 | CNVD |
| Congenital abnormalities | 21549014 | CNVD |
| Developmental delay | 21549014 | CNVD |
| Mental retardation | 21549014 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| Cancer | 20164920 | CNVD |
| Cancer | 17060936 | CNVD |
| abnormal development | 18461090 | CNVD |
| Acute lymphoblastic leukemia | 22237106 | CNVD |
| Non-small cell lung cancer | 21829676 | CNVD |
| Hepatocellular carcinoma | 16750200 | CNVD |
| Arrhythmogenic right ventricular cardiomyopathy | 17576883 | CNVD |
| Multiple myeloma | 16616336 | CNVD |
| Developmental delay | 21147756 | CNVD |
| Ovarian cancer | 21720365 | CNVD |
| Glioblastoma multiforme | 22291905 | CNVD |
| Myelofibrosis | 22110671 | CNVD |
| Disease | 21936942 | CNVD |
| laryngomalacia | 21936942 | CNVD |
| GLUT3 deficiency syndrome | 20509907 | CNVD |
| Developmental delay | 21373258 | CNVD |
| Acute lymphoblastic leukemia | 17443227 | CNVD |
| Developmental delay | 19490664 | CNVD |
| Acute lymphoblastic leukemia | 21098271 | CNVD |
| Acute lymphoblastic leukemia | 21339820 | CNVD |
| Pancreatic cancer | 17952125 | CNVD |
| Non-syndromic sensorineural hearing loss | 18451855 | CNVD |
| Breast cancer | 22522925 | CNVD |
| Non-syndromic sensorineural hearing loss | 22037309 | CNVD |
| Non-syndromic sensorineural hearing loss | 21293372 | CNVD |
| Non-syndromic sensorineural hearing loss | 17122850 | CNVD |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:242383400-242420600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 2 | chr1:242401000-242411200 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
| 3 | chr1:242401200-242420000 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 4 | chr1:242401800-242429400 | Weak transcription | Aorta | Aorta |
| 5 | chr1:242402000-242417600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 6 | chr1:242406600-242411400 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 7 | chr1:242408200-242425000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 8 | chr1:242409200-242412800 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 9 | chr1:242409800-242413600 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 10 | chr1:242411200-242411400 | Enhancers | iPS DF 6.9 Cell Line | embryonic stem cell |
| 11 | chr1:242422000-242422600 | Enhancers | A549 | lung |
| 12 | chr1:242422600-242427600 | Weak transcription | A549 | lung |
| 13 | chr1:242425000-242426000 | Strong transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 14 | chr1:242426000-242427400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 15 | chr1:242427400-242428000 | Strong transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 16 | chr1:242427600-242428000 | Enhancers | A549 | lung |
| 17 | chr1:242428000-242472200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 18 | chr1:242435400-242481400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 19 | chr1:242439000-242439400 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
| 20 | chr1:242444000-242444600 | Enhancers | H9 Cell Line | embryonic stem cell |
| 21 | chr1:242444000-242444600 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
| 22 | chr1:242447600-242448000 | Enhancers | HUES6 Cell Line | embryonic stem cell |
| 23 | chr1:242458200-242458800 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
| 24 | chr1:242458400-242458800 | Enhancers | Ovary | ovary |
| 25 | chr1:242462600-242463400 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 26 | chr1:242466400-242466800 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
| 27 | chr1:242466800-242467200 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
| 28 | chr1:242467200-242467400 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
| 29 | chr1:242467400-242468200 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
| 30 | chr1:242468200-242468400 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
| 31 | chr1:242472000-242472600 | Enhancers | HMEC | breast |
| 32 | chr1:242472200-242472600 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 33 | chr1:242472200-242472600 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 34 | chr1:242472200-242472800 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 35 | chr1:242472600-242477200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 36 | chr1:242472600-242477400 | Weak transcription | HMEC | breast |
| 37 | chr1:242472600-242485400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 38 | chr1:242476000-242481400 | Weak transcription | Aorta | Aorta |
| 39 | chr1:242477200-242477800 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 40 | chr1:242477400-242477800 | Enhancers | HMEC | breast |
| 41 | chr1:242477400-242478400 | Enhancers | Fetal Heart | heart |
| 42 | chr1:242477800-242481400 | Weak transcription | HMEC | breast |
| 43 | chr1:242477800-242485400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 44 | chr1:242481200-242481400 | Enhancers | Brain Hippocampus Middle | brain |
| 45 | chr1:242481200-242481600 | Enhancers | Cortex derived primary cultured neurospheres | brain |
| 46 | chr1:242481200-242481800 | Enhancers | Fetal Brain Male | brain |
| 47 | chr1:242481400-242481600 | Bivalent Enhancer | Brain Hippocampus Middle | brain |
| 48 | chr1:242481400-242481800 | Enhancers | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 49 | chr1:242481400-242481800 | ZNF genes & repeats | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 50 | chr1:242481400-242481800 | Enhancers | Aorta | Aorta |






