Tag | Content |
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EnhancerAtlas ID | HS131-00503 |
Organism | Homo sapiens |
Tissue/cell | ME-1 |
Coordinate | chr1:120665970-120667140 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU4F2 | MA0683.1 | chr1:120666259-120666275 | TTGCATAATAAATTAT | + | 6.44 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_09137 | chr1:120657976-120676855 | CD14 | SE_10518 | chr1:120663764-120667960 | CD19_Primary | SE_30199 | chr1:120664402-120667164 | Fetal_Muscle | SE_37175 | chr1:120665860-120667844 | HSMMtube | SE_43507 | chr1:120649245-120667929 | MM1S | SE_45569 | chr1:120652986-120668944 | Osteoblasts | SE_55738 | chr1:120664236-120667847 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I120121 | chr1 | 120664371 | 120666999 |
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Enhancer Sequence | TTACTAATTA CAAGAAACAG CATTCCCCCA CTCCACCCCT TCATTTCCCA CTCCTCAGAG 60 GAAATCACTT TCAATGCTTT CACTAAATCT TTTTTTAGGG GGAGGAGGGA AATCATTGTA 120 TCTCTAAATA GCTACTTCTT AGTTTTCTCT ATTGACTTTC CACTGTGGAA GATGGGGATT 180 CAGTTTTCGC CTCTTCCTAT ACCACATGGG CTTATATTTC TATGTCATTA TTAAACTGAC 240 ACTCAGTGTT TATATTACTA TGATCAAATA AATACTATTC ACACCTGTGT TGCATAATAA 300 ATTATGATCA CTTTCTTCAA AACTATTTTG CTTCCTCTGG AGTTAATAAT TGTCTCATTT 360 TTCATTTGCC TAGTTTTTCT ATGCATATGC CACTAATTTA ATCCATACTC CTCTGTAGTT 420 GTTTAAGTCT CCTCTCAATA TGTCCAAACA AACTTGGTAT TCCATCAGTT TCATCTGGAA 480 GAGAGCTCTT CCAGAGCCTA CTGATCTGCT CCTCTCTGGG CTAACTGACC TCTAGGCCTG 540 CTGTGCATCT GTCATCTTGG GACTTCCCTT TACCCACATC CTGGGGACTC TCTTCACCTC 600 TGTGTTGAGT GCTCTGGTTC CTGAATTCCA CCTCTTCCTC TTTCTTGACT CACAACACTG 660 TTTTGGTGGA GCACATTCTT CAGTAGTTTC CTAAGAGAGA GTGCAGGGAA GATATAGCAT 720 TTGCCATCAG TGCCCTGCCC AAATTCTCTT GGCACTTAAC ATCCAGGCCT TCAAAACTGC 780 CAGCACATAT GTCTGTTTGC CTGAGGGCTT TTTCTAGCTA CTGAAAGTTT GCTCAGGAAG 840 TGTTGGGGAA TTAACCCCCT TTTCCCTGGG AGAGACCCTT AACCAATGAC TGATGAGAGT 900 TAGTAGATAA ATATCCCAGC TTGCTCAACC ATGAGGGGGT TTAACCCTGA AGCATGCTTT 960 CTACACAGGT CTCCCAGAGT TCCCCGATGG AGTCAAGTTC CACTGGTTCA CAGTAACTTG 1020 CAAGATATAT TAACTTCCGT AGGATCCTTT TCTCGTTACT TTACTCCCGT ACAGATGTTT 1080 ACTGGGGTCA TCTCCCAAAT AAACTAATTT TGCTCTTATA TTTTTTATTT TCCATCTGTT 1140 ATCTTTCTGC TTTCCTTTCT ACTTTCCAAA 1170
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