Tag | Content |
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EnhancerAtlas ID | HS187-10344 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:34393100-34394730 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2F1 | MA0017.2 | chr17:34393627-34393640 | CAAGGGTCAAGAG | + | 6.3 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_20564 | chr17:34391231-34398490 | CD56 |
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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 |
GH17I036065 | chr17 | 34393171 | 34394778 |
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Enhancer Sequence | ACAAAAGGAA CTAAGGAAGT CAGGCATTCA TCCTTGACTT TGAGTGTTTC TTTTAAATCT 60 CTGCCTCTGT CTTACTCTCA CTCCCTTGCT CCCTCTTCAG GGAGTATAGC TCTTGGAATG 120 GCTGGCCTTT GTTCCATCTC TTTTGGGTAG GAACTTCATT CAGTCTACAG AGACTTTTCC 180 CAGCAAGAGA CCATCATCTC TAAATCGCTG TAGGAGTAGA GCTTCTCAGG AGAACTGAAG 240 GAACTCTGCC ACTTCCTCAC CCTAGGAACC AACTAGACCC AGAGTTTGCA TCTTGTGAAT 300 GACTGAGTTA GGCCCCAGTT TTCCCAACTA ACAATGGGTC CTAGCCCTCT CCTGCCTTTC 360 AGATCTAGGT TAGATATCTA AGTCCTCAGA AAATAGCCCA GAACATTTTG AAACCTTTTG 420 TGAAGTTCTT TGATTTTACT TAGAGAATCT TAATCCACAA GAATTAAGTG ATATGGCTTA 480 AATGTCTGTC CAGAGCATAG GGAAACAACT CTAAAATGAA GAAAGGACAA GGGTCAAGAG 540 AGTCTCACGG GACAGATGAG ACTTGTGAGC TGAGGGCCAT GGAGAGGAGA TGGAGGGCAC 600 CAAAGAAGAC CTGTTCAGTG TTGGGCAGGC AGAGGAGTGT AGGCAATGCC AAAACAGGAC 660 TGGGCACTCA CTGCCACCTA CATCGTTCTG GGGTCCAAGC CATGTCCTCA ACCCTTTACA 720 GGCAACTCTA AACCATGAGG AGCTGGAGAC TGGGGATGAC CAGAGGGGAA GATGTTAAGT 780 GCATGGTGTC TTGCTCTGAG TTGTACATGT TGGGGTACCT TGGGTCCCCC AGGGGTTCAG 840 GATGTACAAG AGCAACTCAA CTGCTCACTT GTTGGGGCTG AATGTGCAGA AATGTTTTTG 900 ACAGTGAGAG AGGGTGAGAT GTTAGTGTTG AAGTCATACG TACAAGGAGA GATCTTCAGA 960 TTAACACTTC CACCACAGAG CAGCTCTCTA ATGCTGTGCT GCAGCTCCTC TGACCACATG 1020 GTGTGATGTA AATGGTCATG CCACAGCGTT CTGGGCAGCA CAAGTCACAT TTAAACCACA 1080 CCCTGGGTGA AAAGGACCAT TACATCGTGT TAATCGGAGT GCTTCTAAGA AATGCTTAAC 1140 TCATGAGGAG GACGTCAAGA ATTGGTGTTA CCAAGAAGCC AAGCTTAGCT GGTACCTTCT 1200 ATCAAGAACA GATCTATTTG TGAATGGCAC CATGGTCATT TCCTCCTATG GAACAGATAT 1260 TTCTAGTGTT GTGTTTCCAT TGCACAGAAG TGACATGTAA GATGATACCC CAGAATCTTA 1320 AGTAGTTCGA GTTGTGTTTG ATCCAGACCC AAATGGACAG AATGGAATAG GGAAAGTCTG 1380 GACTATGGGA ATGACAAGAA TGATGGGGCC AGGCTTTTAA CTGCTGTTTG ATTCATTGAA 1440 CATTCATAGC TCCCTACAAT ATGCCATCAT TGGGTTTGAC TCTGGGTAAT AGACATGAAT 1500 ATGCATGACA TATGGGGTGT CTATATAGAT CAGGAGCCTT AGATGCCCTT ATTTTTTCAC 1560 CCAGGAAGCC CACAGCTAGG AAAATATCCT ACAGAAATAA CCTCACTTAT GGAGAAAGTT 1620 TTTTGCATAC 1630
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