Tag | Content |
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EnhancerAtlas ID | HS141-00935 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:117533060-117534370 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:117534002-117534020 | CTATCCAGCCTTCCTTCC | - | 6.38 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_09895 | chr1:117531489-117538208 | CD14 | SE_56636 | chr1:117529960-117535257 | u87 |
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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 |
GH01I116986 | chr1 | 117529027 | 117534708 |
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Enhancer Sequence | TTTAGCACCT TCTGATCTCT TTGAATCCTG TAAAAGCATT GCAGATTTTC ACTAATGATA 60 AGAGAAGAAA TGGATTTGAT GGGATCAATG TTGAAGTTCC CACCGGGTGG AAAGGTGAGG 120 GCTAGGATCC TATTGTTTAC AGAAGGCCTC CTGCTCTTTC AGGGAATTCC CATGACCTTA 180 CAGGACTCCT CTCAGGAAAG AGAGAAGTTA GATATTGTTC CTCTCTGCAG TTGAGGAAAC 240 ACCAAAGTTC TGTGACCATA TCGTGACTGG AACGGAGTGG TTTTTCTGAC TCATGATGCA 300 GTCTGGGGCC AAATCAGTCC AGAAGGTAGC AGCCCCTGTA ATAGAAAAAC AATCGTCTTC 360 CCTAGGCCGC TGGCGTCAGC AGGCCTGGGC AGGAGTGAAT ACCGAGAACC CAACTCCCTG 420 CGGGCCCCTG GAACAGCTGC TTGCCCTTGG CTGGCCTCCG CCATTCACTC TCCTCTTGGC 480 CTCGTTTGCA TTCTCTGTCT TTTGTGTCCT TTCCAGGGAC CAACTTCATG TTGTGGAGTT 540 ATTCAAGGGC TGGGTCCGTG TCCCAGTCAC TAACATTACC CAATGACTGG CACTCTTCCA 600 GGCATGTAGA AGGCACTTGC ACTTTGTAAA TGCACAGTTA ATGCTCTGCT CTAGGAAATG 660 AGCCATCATT GCATGCTTCT TAGCGAACCG GGAGGGTTCC ACTCATGTCA CAACGGTAAC 720 ACGGTCAGAG CTGGTCATTA GCAATCCTCC ACCTATTTCT GAACCCATTC CTGCCTAAAA 780 TTTAAGTTAT AAATTTATAT TAATAACATT AAACTAAATT AAAAACAAAA CAGGAACTTA 840 CTTGCATACT TATTGTGTGC CCAGGCATTG TGCTAAGCAC AATTGCTGCT GAGTTGTCTG 900 TAGGCCTTGG CACATAGTAT CTGCTTGCCT AGAAACTTAT TTCTATCCAG CCTTCCTTCC 960 TCCTAACTTG TACTTCTCTT TCAGGACCCA GGGGTCATCT TCTCCTTCTC TAGGCAAAGT 1020 GAAGGTCCCT TGACAGATGG TCTGATAGTC TGAAAATGAT GGGAGGATAG GAACCATTCA 1080 TTGCTGTGGC TTCAGTACCA AATTGTGAAT TGGACTCTTA CAATGTGCCA TGCACTAAGA 1140 CAAGTACCTC ATAGATGTGA TTGCAATCTT AAGTGACCCA AAGGGATTTA CAGCAGAAGC 1200 ACTCTTGCCT GTTCTTCACA AAACTGGATC ATTCAAAAAA TACCACTCAC TTCCTCTAAC 1260 CCACAGACCA GTGTGTGTGA CACACTTTTA AAATGAAAGT TTTAGTATTA 1310
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