Tag | Content |
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EnhancerAtlas ID | HS101-38762 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr6:144670250-144671390 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr6:144671128-144671142 | GGAAGATGACTCAT | + | 6.77 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_00127 | chr6:144667622-144687584 | Adipose_Nuclei | SE_09965 | chr6:144667150-144676515 | CD14 | SE_10740 | chr6:144670118-144673365 | CD19_Primary | SE_12337 | chr6:144670397-144674042 | CD3 | SE_13279 | chr6:144670348-144672143 | CD34_Primary_RO01480 | SE_16847 | chr6:144670603-144673643 | CD4_Naive_Primary_8pool | SE_18900 | chr6:144663590-144677537 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20379 | chr6:144667238-144680806 | CD56 | SE_22651 | chr6:144662837-144680967 | CD8_primiary | SE_63161 | chr6:144654983-144686398 | 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 |
GH06I144346 | chr6 | 144667326 | 144677972 |
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Enhancer Sequence | TCTCCTGCCT CAGCCTTCCG AGTAGCTGGG ACTACAGGCG CCCGCCATCA CGCCCGGCTA 60 ATTTTTTGTA TTTTTAGTAG AGACGGGGTT TCCCCGTGTT AGCCAGGATG GTCTGGATCT 120 CCTGACCTCG TGATCCGCCC GCCTCAGCCT CCCAAAGTGC TGGGATTACA GGCATGAGCC 180 ACGGCGCCTG GCCCTGAGCA GTTCTTTAAG GGATGAGACT TGGCCCTCAA GATCTGGGTT 240 TCCATTACCC CTGCCATCGT CAGGGTAAGT CACTGAACCT CTGAGAAGGG GACTCCCAAC 300 CAGGAGGATC ACAGGATCTC CCAACCAGGG AGGATGCCCC GGGAGAGTGT GGTCAGGATT 360 CATGATGTTA CACATTTTAA AGTTCTTTGC AAGCTATAGT AATAGTTCCA GGTAAATAAA 420 TGGAATAATA AATTCTGTAA AAATTATAAA AACCTAGTCT GTTGATAATG GGCTCTTTTA 480 GGTAGAGTCT AGGGTAGGAA ATCAAACATT ATATTCATCA TGGTACTTGA AATATATTTA 540 AGCTGAAGCT GTGCACTCCA TCATGTTTTT GATATATTTT TCCTTGGCAT TACTTGAAAG 600 GCATGCTCAT GAAACTGGAT TTGGATCTGT TTCATGTTTT CACTTGCGTT CTCTGACCCC 660 TACTTAGAGG GCACCAGGTG CTTCCTATTC TAACCGTTTG CAAATTCAAG ACTTGGTTGG 720 AGGGCCATTC AGGGGACTGG TGTGGGGTTA GATAGGATCT GGACACAGCG ACTCCCTCGC 780 TCCTGCTCCA GTATTTTGAC CTTAATTTGA ACAGTTCAAT GAACTGGCAA CTGAAGTCGT 840 TTTTTCCCAC TGAACTAGAC CTTTCATTGT TTTGCAGAGG AAGATGACTC ATAGCCAGGT 900 TCTACCATTG TGCTAAAGTG AAATTTTAGT CTAGGACTAA AGGAACACAG GCCAAACTTT 960 CTGTCTGAGC TGCAGAGTAT TGAAACTTAG ATTGTGAGCT GGGCAGGAAT TCCTGTGGCC 1020 CTCTGTGTGG AGTTGCTCTC AAGGAAAAGG AGCATTTAAA TACGTTTTTG ACTCCAAATT 1080 TAATTTTTAG TAATATAGTT CAAATGTCCT TTAAAATATC TTAAGTAATC AGACTGTTTT 1140
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