Tag | Content |
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EnhancerAtlas ID | HS187-13395 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:70001500-70003010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr2:70001861-70001872 | CTCTGTGGTTT | + | 6.14 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27649 | chr2:70001945-70012834 | Fetal_Intestine | SE_28548 | chr2:70001663-70014048 | Fetal_Intestine_Large | SE_31933 | chr2:70001543-70003068 | Gastric | SE_53176 | chr2:70002283-70002956 | 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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I069761 | chr2 | 69988613 | 70010508 |
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Enhancer Sequence | GCTCTTGTTG CCCAGGTTGG AGAGCAGTGG CGCAATCTCA GCTCACTGCA ACCTCCGCCT 60 CCCAGGTTCA AGTGATTCTT CTGCCTCAGC CTTCCGAGTA GCTGGGATTA CAGGCACCCG 120 CCACCATGCC TGACTAATTG TTTGTATATT TAGTAGAGAC GGGGTTTCAT CAGGTTGGCC 180 AGGCTGGTCT CAAACTCCTG ACCTCAGGTA GTCCACCCAC CTCGGCCTCC CAAAGTGCAG 240 AGATTACAGG CGTGAGCCAC CGCGTCCAGC CAAAAGGAGC CCCCTTAATC ACAGCGTTTA 300 CCATGACCTG GGTAACAGGC ATATTCAGCA GACAAATACC CCGATGATCA TCAAGCCAGT 360 CCTCTGTGGT TTGCATATGA AGCACATCAG CTGCTTCATC AGGGGTATTC TACTTGGCAT 420 TTATAAGGGG AGAGGAACAG TCCCCCTTCT CAGGGTAAAC AGACCTTAGT GTGGCTTTTG 480 TCCAGTCCAC CAGGCTGGAT GTTCTCTCAG GAATAACCTC CTATGTGTCT GGACCACCTG 540 AAACATCTGC GATTGCTCCA TAGAGAGCTG TGGGTCCTGC ATCAACCCAA ACATGAATGC 600 TAGCATTTTG AATACTCTGC AGTGTTCGAA ACCTAAGACA CTGTCACTCA CTTAGTTACT 660 CACACAACCC ATTTGAATAA AGGTTCTTCA GGAAGTTTAT GATACTGATC TACAAAATGA 720 AATAACTTCT TCACACTATA CCCTGTGGTT TCAATCGTTT CATGGTTTGC CTTCCACCCC 780 ACATAAACTG CCTTCTTGGT TACCAGAGTT CTTAGTGATA TTGTCTAATC TCAGCATGAT 840 TTTGCCATTG GTGGGTGGCT TTGCAGTTAC TGGCTAGAGC GCAGACTCAC TGAAATCTGA 900 GCTTGGTCTG ACCCAGCACT CTCTTTTAAT TTTATTTTAT CTGTTACAGA TAATAACCAA 960 GGGACTGAAT ATATCGCCTT TTCTTATTAG TTTGCATTTC CTTATGCTTC CAGTGAGCCA 1020 ACACCTTGGG GTAGCTTTTA CCTTTACTAA CAGATCTCAG CATGGTATGC TACTCCGTAC 1080 CATGAGTGGC TGTTACCAAT GCCATGGGTT CTTGTAATCA CCCAGGATAG AAATCAAGAG 1140 CAATCACCAT ACATAGCAGC AAAGAGAAAG TTTGTTTTGG CTCATGCACA AGGGAGCCAG 1200 TGCTGAGAAA GGAAAAGAAA CAGACTGCTA TCGGAGGATA GTGTGTGGGT TAGTTTTATA 1260 GGGTCTTTCC ATGGGAAAGG GTTACATCAG AGCATGTATA GGAGAGGCTT TTCTAGCACT 1320 CATGCTTCTT CATGCATCAT ATGCAACATT AGTATTTTAA ATCTCCACCC CATGCATTTT 1380 TAGCCTTAAA ATGAGGAAGG GTAACTGTAG GTTGGACTTT AAGTCTAGCT ATGCATGCAG 1440 GGCTCCAGGG AAGTCCCCAG CCCCCTGAAA TAGGAACTCG TGGTTAATAA GCTTCTTGGG 1500 TCTTTTGTTA 1510
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