Tag | Content |
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EnhancerAtlas ID | HS197-02737 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr10:70985740-70986960 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LHX2 | MA0700.1 | chr10:70985880-70985890 | GTTAATTAGT | - | 6.02 | TBP | MA0108.2 | chr10:70985763-70985778 | GTATAAAAACAGGGC | + | 6.03 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27984 | chr10:70979065-70991295 | Fetal_Intestine | SE_28850 | chr10:70979061-70987098 | Fetal_Intestine_Large | SE_53047 | chr10:70984148-70986283 | Small_Intestine | SE_53047 | chr10:70986422-70990508 | Small_Intestine |
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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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Enhancer Sequence | ACCTGGAGGG TGGAGAGTGC TCAGTATAAA AACAGGGCTG GAAAGGACAG GGTGCATATG 60 CCCCTGTCTC TCCTCCTGCC CCCATCAATA ATCCATCCCA GTGAGCCCGG GCTCCAGACT 120 GCCAGCACCA ATTGATTAGT GTTAATTAGT GTGAGGGAGG AAGCTTTGCT GCCGTCCCTG 180 ATGTGACATA TTACCAACAA GAGGACTGAT TTTAGCCATA GTGATTTGTA TAACTTCCCT 240 CCTTTGGGTA TGGTCCTCTG TCCCCGTTTC CTGGTTACAT GAGTGACATC CACTCATTTT 300 CAATAGCAAT CTGAGCTGAC TTTAAAAATT CAGCTTTGTC TTAACTAGAA CAACTCAGTT 360 AAACCAAAAT GGACATTTAT GGCTGGGTGA GGTGGCTCAC GCCTGTAATC CCAGCACTTT 420 GGGAGGCCGA GGCGTGTGGA TCACTTGAGG TCTGGAGTTC AAGAACAGCC TGGCCAACAT 480 GGCGAAACCC CATCTCTACT AAAAATAAAA ATAAAAAAAA ATTAGTCGGG CCTGGTGGCA 540 CCTGCCTGTA ATACTAGCTA CTCAGAAGGC TGAGGCAGGA GGATGGCTTG AACCTGGGAG 600 GTGGAGGCTG CAGTGAGCCG AGATCTCATC ACTGCACTCC AGCCTGGGCG ACAGAGTGAG 660 ACTCTGTCTT AAAAAAAAAA AGGAGGGAAA TTTAAAGGGC TAGATTTAGG CATTGCTTTT 720 GGAAATGAAA TTTAGCTCTG AGCTTCCTAG CAGCCAGTAA ACAAAGAGAA ACCTGTCTAG 780 CTATATCTGT GGTCATCATT GGATGAAAGA AAGCTTCCAT GTTTAGAAAT CTACGATTCA 840 AGCTCTAGCT GGCCTTTTTT GGTGGAGAGG AATGGGACAC TGGTGAGGGC CCTGAACTGG 900 GAATCGGAAA CCCTGAATCC TTCTTAGTTT CTGCCTCTCC CTTGTCTCAT CAGAATAATG 960 GGAGAATCAT TTTCTCCTCA GATTCTGCCC TTCAGAGAAG TAACTCCACA CCTTCTCAGC 1020 CCTCCGTTCC ATTCTGCTTT CCTAACTCGC TTCCCTGTCC TCTGCCTGAG GAGGGGTCAG 1080 ATAGGGAGGC TTTGGGAATC CACATCTCAA TGCTGTCCCC AGAGTCAGGA ATGCAGCTTG 1140 CTGAGGGATG TCGGGGGTTA CAGCCTCGAC TGGAGGGTGA GGGCCCCCAG CAGCACCCCT 1200 TGGTGGCCGG TGTCTGTTCC 1220
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