Tag | Content |
---|
EnhancerAtlas ID | HS052-00471 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:20800700-20801950 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6 | MA0677.1 | chr1:20801321-20801335 | TGACCTTTGAGCTC | - | 6.6 | Rxra | MA0512.2 | chr1:20801321-20801335 | TGACCTTTGAGCTC | - | 6.3 |
|
| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_05163 | chr1:20797832-20802020 | Brain_Cingulate_Gyrus | SE_06168 | chr1:20800960-20809454 | Brain_Hippocampus_Middle | SE_06941 | chr1:20801073-20814394 | Brain_Hippocampus_Middle_150 | SE_23263 | chr1:20801049-20801940 | Colon_Crypt_1 | SE_24162 | chr1:20801308-20801917 | Colon_Crypt_2 | SE_24976 | chr1:20801507-20801966 | Colon_Crypt_3 | SE_27987 | chr1:20800622-20814579 | Fetal_Intestine | SE_28809 | chr1:20799528-20814863 | Fetal_Intestine_Large |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAGCCTAGGA AGTTGAGGCT GCAGTGAACT GTGATCACGC CAGTACACTC CAGCCTGGAC 60 AACACAGCGA GACTGTGTCT CTCAAAACAA AAAATAAAAA CAAACAAAAA AAGAGCTTAG 120 TGCAGGGCCT GGCACTTCAT AAGTGCCCAC AGAGACTTGG TAGTGGTGTA GTAGTAGCAA 180 TCCTCAGTGG GCTATAAGGA CTGGATGAGA TAACACACAT AAAGAATTTA GGGTTGTAAC 240 TGGCACACAG TACTCATGAA ATATATGGCA GTGATTTCCT TAAATGCCGT TAGCTGTTAC 300 ATCAGCCCAT TTTAGAGAGA AGGGAACTGA GGAATGAGAA CTTAAGTGAC TTGCCCTAAA 360 TCTCACTTTA AAGGCTCTTA AGCAGGCTCT AAACTAGTAT TTCCTAACCT CAGCACATTG 420 CTGTTTGAGG CTGAATCATT CTTTGCAGTG GGGCTGTCCT GTGCACTCTA GGATGTTTAG 480 CAGTATCCCT GGCCTCCGCC CACCAGATGC CAGTAGCACT AGCCCTCTCC CCAGCATTTT 540 GACAACCAAA AATGTCTCCA GACATTGCCA AAGTCCCCTG GGGGGCCAAA TCAGCCCCAG 600 CTGAGAAGCA CTGCTCTAAA CTGACCTTTG AGCTCATATA TGAAAAACCT CCTGATCTAG 660 CCCTAACCTC CTTTCCCCCA GTCCCAACAC CACCACAAAT GCCTTGTTCC AACCAGCCCC 720 TAAAGGACTG CCCTTTCTCA AGCAAACCCC AAACTTACCA ACATCTGTCC CTCTGCTCAA 780 GAGTGACCTT GCCACCCCAT CCCCTTCTCC AAGGCCCCGC TGAAATCCCG CCCACTCATT 840 AAATGGTCTC CTCACCCCCC AGAACACGTT GTTTGTCTGT GCCCAGCCTT CATCATGATG 900 GGCATTTCAT TTTATATCGC ATCTGATCGT GAGCATATTC ATGCTTCCCT GTTCCCTGTC 960 CCTCATACCC ACCCCCAACT CCAGGGGAGG GGCTGTGCCT GACTCACCCC TGTGTCCCCG 1020 GCACCCTGCA TGGGGCCAGG CACACAGGCC GGGTCATCAC TCTGTGCAGA TGGTTGTCAT 1080 AGATGAGACT GGTGCCCAAG CAGCCTCTTG GATGCTGGTG AAGGACCCCC AGGTTAGAAG 1140 GCAATGTGGC ATGGAATTTA GGAGTGGTTA AGAGTTCAGA GTGGGGGCCG GGCGTGGTGG 1200 TTCACGCCTG TAATCCTAGC ACTTTGGGAG GCCAAGGCGG GCGGATCACC 1250
|