Tag | Content |
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EnhancerAtlas ID | HS042-34369 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr4:7935340-7936590 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr4:7936484-7936499 | GCTGACCTTGACCTC | - | 7.82 | RARA(var.2) | MA0730.1 | chr4:7936492-7936509 | TGACCTCTGACTGCCCT | - | 6.14 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27581 | chr4:7935781-7936564 | Esophagus | SE_36928 | chr4:7934754-7936972 | HSMMtube | SE_45546 | chr4:7935163-7938250 | Osteoblasts | SE_47152 | chr4:7934278-7936787 | Panc1 |
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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 |
GH04I007933 | chr4 | 7935248 | 7936548 |
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Enhancer Sequence | TGAAGAAGAG AAATGCGCCC AGGGGAATTG GAGGGCCTGA CCAGGTCCCT GGCCTAGCTA 60 GTCCTGAGCT GATGGGACCA CATGCAAAGA CCAGATAGAG GCCTCAGGAG CTGAGGACAG 120 CCCCCAACAG ATGGCCAGCA AGGGGACACC TCAGTCCTGC AACCACAAGG AACTATATTT 180 GGCCAAAAGT GCTTGGAAAC AATTCTCCAG TGAGGAATGC AGCCCAGCCC ACATGGTGAT 240 TTTTGCCCAG TGACACCCAC GTCAGACTTC TACCCCACAG AACTGTGAGA TGATACAATT 300 TCAATTATTT TAAGCCACTA AATTTGTGGA AATGTGTTAA AGCAGCAACA GAAATGAATA 360 TAGTGATTTA CGTGGAAATC CCTAGCGGAG TGTCTGGCAC GGTGTTGACA TCTGACAAGC 420 GTTTCCTGAT TTCCTTACAT CCAAAGGCAG GGCTGGCCAC ACTCCATCCA AAACAACAGA 480 TGATAGACTT GTTCTGACAG AACAGATACA GTGAATTATA AATGGCCCAG AACACCTACA 540 AATTTTAGGT TTCAGGTAAG TGATTGCCTT TCCTTTCACT TAGAAACCTC CCAATGCTTG 600 TCTTACTGAT AAGCTCTAAG TACCACACAG AAGACTAAAC ACCAGACTAA CCCGGCTCCA 660 GATGCCCCGA GGGAGCCCAA CCCAGCACTC ACTCTGCTGC ACTGAAATGA TGTCCAGGTC 720 GGTTTTTCCC ACTGGACCAC GAACTCCAGC TCTCCACGTG TGAGTCACGA GTCCCACTTC 780 TGCATCTCTG CTTCTAGAAC GGTGCCCCTG CACTTCACAG GAAATCTGTA TCCGTGTTTG 840 TCAACACTAT ATATGACAGT ATAACTTAGT ATGTGCACAG AAAACATAAA TTCTTCGAGG 900 ACCAGGGCCG GGTTTATTAG CCTTTGTACT CCCACTACCA CTGTCTGGGA TATCAGGGGC 960 ACTCAGGAGA AGTTGGTGAC GAGAAAGAAA AGGCAGAGGA GAGAGAGGAA AGCAGGCCCG 1020 ACACCGCACA CACAGCTTCT GAGGTGGCTG GAGGAGAGGC AGGTGCAGAG AAACTTCCTG 1080 GGTGCTGGAC TGGGGTTCAC TGTGATGCTG CTGCTGGATT TCAAATGTCA AAATGTGATG 1140 CTTTGCTGAC CTTGACCTCT GACTGCCCTT TAGTTTTCCC AGCCTCAAGA CAGGGCACTT 1200 AGAAACTGCA ATGTCAAGAA ATTACGCTTC GCTAAAGCAT GGGAATGCTA 1250
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