Tag | Content |
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EnhancerAtlas ID | HS113-37482 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr9:33150930-33152200 |
Target genes | Number: 13 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr9:33150982-33151000 | GGAAGGAAATAAGTAAGG | + | 6.5 | EWSR1-FLI1 | MA0149.1 | chr9:33150978-33150996 | GGAAGGAAGGAAATAAGT | + | 6.7 | EWSR1-FLI1 | MA0149.1 | chr9:33150962-33150980 | GGATGGAAAGAAGGAAGG | + | 7.73 | EWSR1-FLI1 | MA0149.1 | chr9:33150974-33150992 | GGAAGGAAGGAAGGAAAT | + | 9.03 | EWSR1-FLI1 | MA0149.1 | chr9:33150970-33150988 | AGAAGGAAGGAAGGAAGG | + | 9.09 | EWSR1-FLI1 | MA0149.1 | chr9:33150966-33150984 | GGAAAGAAGGAAGGAAGG | + | 9.47 |
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| Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
SE_00330 | chr9:33150154-33152533 | Adipose_Nuclei | SE_00992 | chr9:33150845-33151621 | Adrenal_Gland | SE_03080 | chr9:33150830-33151209 | Bladder | SE_09459 | chr9:33150683-33152077 | CD14 | SE_10229 | chr9:33150691-33152191 | CD19_Primary | SE_10912 | chr9:33119344-33169982 | CD20 | SE_19329 | chr9:33150695-33152114 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20045 | chr9:33150690-33152312 | CD56 | SE_22416 | chr9:33150710-33152253 | CD8_primiary | SE_23687 | chr9:33150875-33151683 | Colon_Crypt_1 | SE_26031 | chr9:33150287-33152385 | Duodenum_Smooth_Muscle | SE_26859 | chr9:33150779-33151670 | Esophagus | SE_27770 | chr9:33149455-33152321 | Fetal_Intestine | SE_28724 | chr9:33149325-33152320 | Fetal_Intestine_Large | SE_29800 | chr9:33150488-33152194 | Fetal_Muscle | SE_31534 | chr9:33150777-33151683 | Gastric | SE_34775 | chr9:33150487-33152230 | HeLa | SE_40894 | chr9:33150769-33152080 | Left_Ventricle | SE_41831 | chr9:33150862-33151334 | LNCaP | SE_42236 | chr9:33150804-33151823 | Lung | SE_44340 | chr9:33150635-33152125 | NHDF-Ad | SE_45447 | chr9:33150452-33151912 | NHLF | SE_45731 | chr9:33149399-33152178 | Osteoblasts | SE_46917 | chr9:33150883-33151589 | Ovary | SE_47814 | chr9:33151298-33151559 | Pancreas | SE_48426 | chr9:33150761-33152145 | Psoas_Muscle | SE_48738 | chr9:33150773-33151797 | Right_Atrium | SE_50176 | chr9:33150800-33151701 | Sigmoid_Colon | SE_51651 | chr9:33149245-33152315 | Skeletal_Muscle | SE_52621 | chr9:33150782-33151822 | Small_Intestine | SE_53402 | chr9:33150804-33151863 | Spleen | SE_56627 | chr9:33150139-33152742 | u87 | SE_58985 | chr9:33124740-33168862 | Ly3 | SE_62118 | chr9:33106994-33169093 | Toledo | SE_62346 | chr9:33106942-33169226 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I033149 | chr9 | 33149003 | 33152397 |
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Enhancer Sequence | GATTATTGGC CATGAAAGGA AGCTTGATGG CTGGATGGAA AGAAGGAAGG AAGGAAGGAA 60 ATAAGTAAGG GAGAGATGGC GGATGGAGCT GGATGTGTCC TTCCAGGGCT GTACAAAGGA 120 GGGGGACCCC AACCCCTAGT CCAGACAAAG GTCCCTAAGG CAGGTGTACA GTATTGTGGG 180 GATGAATTCA TCAGCCACGA GAGACTGACC CATCTAATGT TAAATTCACT TCCCTGCTCT 240 GACTGCTGAC TCACCAGCAG TTAGCTTATC CTGCGGCTTC CCTTGCAGTG AATTCAGCCA 300 GAGATTTCTA AGCTACTCAA TAACAGTTCT AATCTTCCCA GTAAAGCTGC AACTTTGCAT 360 TCCAGTATGT AAGTAAGTCT CCTGGGAGTT TTATTACTGA GTCAGCTGCC CCTCTAATCA 420 GTTTTGGAGC CCCAGCAGAT TTTCTGGAGC TGCGGTGCTG ACTACGAGCA CATCCTTCTC 480 TCTCCACCTA GAACCAGACC TTGGACTGTG GAGGGCCCAC TACTCCTATG GGCCATCTGG 540 GCACTCAGCC AGCCAAGTAC TCCTGGCAAT ATCTCTCTGG TGTCAGGACT ACTTTAAATG 600 TAGCCAGCTC CAATTTCCTT CTCTAAGGAG TGGGGATAAT TATGCCTTCC TTTCAGATGT 660 AAGTGAAATA ATACATATAC ATACTTATCG CATGTTCTTA TTGAGCTAAT AGATGTTCAA 720 TAAATGTTAC TTTCCCTTCT CCCCTGACTC CTTAGAACTT CAGAGCTTAC AAATTACTAC 780 AGCTCTATCA GCACACATGG CTAAATTTTC ACATTTCTAC TCTTAGCCAC TAGAATCACT 840 GATAGATTTG GAGGAAAACT CTGGGACCTT AAAGGGTCCC TGGAGTATTA CATAAAGCTT 900 CTTGCAGCAT GAGAGTTGAA CAGAAATTCT GTTCATCTTT TGCTGTCGAA GCCAAGTTGG 960 TGGCTTCTAA AGAACCAACT TAGAAGAAAA CTCAGGAGAA AAATTTTATC ATTTTGGGAT 1020 GGTGAAGACC TGCTTAAGTA TGAAAGCAAC CTGAAGTCAT AAAGGAAAAC ATAGATTTAA 1080 ACACATAAAA ATTCAAAACT TCTGGCCGAG TGCAGTGGCT CACGCCTGTA ACCCCAGCAC 1140 TTTGGGAGGA TCATTTGAGA TCAGGAGTTT GAGATCAGCT TGACCTACAT AGTGAAACCC 1200 CGTCTCTACT AAAACACAAA AATTAGCTGG GTGTGGTGGC GGGTGCCTGT AATCACAGCT 1260 TCTCGGGAAG 1270
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