Tag | Content |
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EnhancerAtlas ID | HS099-01258 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr1:116692910-116694340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT3 | MA0144.2 | chr1:116693672-116693683 | TTTCCCAGAAG | - | 6.62 | TCF3 | MA0522.2 | chr1:116693820-116693830 | AGCAGGTGTT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 116693662 | 116693900 | chr1 | 116694109 | 116694251 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I116150 | chr1 | 116693441 | 116696470 |
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Enhancer Sequence | GACCTACTCT TGCCCCCCGA CCTCACACCA GTCCTCCCCA CACAAGAGCA AGGGGGGCAA 60 CCTGCAAACT CAATCATGCT TATTTTCCCT GCTCTCATCC TCCCAATAGC TTCTCATCTC 120 TTAGGAAAAA AAAAGGGAAA CTCCCCACCA AGGCCCACAA GGATTATGTG ATCTGACTTG 180 GGCCATTCTC TCTTTCCTCG CCAACTACCA CGCTCCTTCA CACTGTTCCA ACCATACCAC 240 ACTGGCTTCC TTGCTTTGCT TCAGACACCC AAGCTCCATC CTGCCCAGGG CCTCAGTACC 300 TGTTTCCCCC TTTGCTCAGA AATCCCATGC TCCATGCTGA CATGTCCCAA CCCTCCCCGA 360 ACAGCCTAAC ACAGCTAGCC CCCAGCACTC TTGCCCTGCA CCATACTTCA CTCTCCCCAT 420 AGTGGTTTGC TGGTTCTCCT ATTAGAATAA ATATAAACTC TATGCCGGGA GAGGGCTTGT 480 CTTATTCACT GTTGTATTAT ATCTCCGGCA CTTGGAACAA TGCTCAGTGG GTAAGAGCTC 540 AATGAATAGT TGTTAAATAG ATAATTGCAT GAAGGAATGG ATGAATACAT GATTTTGCTC 600 CATAATATGT ATCTGCTTTG TGGCAGGGCT TGGATTTGAA CCCGGGTCTT CTAATTCTCA 660 GGCCAGGCTC TTTCCTCTAC AAAGTAACAT TTTGAGAGTC TGAAGAATCC CACATCTTTA 720 GTTTTAGAGA AAGAAAAATT GCCTCTGGCT CCAGAAGCCT GTTTTCCCAG AAGGGCCTGG 780 CTGTCCTCAC TATGCAGAAC ACAGCTTGAT GCAGCAGAGC TTGAGAATGC ACACTCATGC 840 TGCAGAGGGG CCAGCCTGGC AGCTCATCAC AGCAGCCACT GACAACTGTG GGCACTGGTG 900 GATACTTTGT AGCAGGTGTT TGCTGGACAT GCCTAGCTTA ACTGGGTTCC AACGTGCAAC 960 ATGTAGACTG AACAACACAC ACACACACAC ACACACACAC ACACACACAC ACACACACAC 1020 ACACACTGCA TTTAAACAAA GCACATCAGA AAAGAGTTCA GGCTTTCACC CTCCCTTCCT 1080 GCCAAGCACG GAGACAAACA GTACTGGTCT TGGTTCTCTT TGTCTCTGAG TCTAGACCAT 1140 TCATTTCCTC TCATTCAACC AGCTTTATTT TTGGCGATGT AACTTTCTTT CGTGAGCATA 1200 TATATTATGT TCTCAGACTT TGTAACCTAT GAATCTCCTG TGAGGACCGA CCTACGAATG 1260 CTCAGAATAC AAAGGCCGGA GTGAGCAGTG CTCTCTGTGA GAGAGAATGT TACGGCAAAT 1320 GAAAAAACCA CCTTCACCAC CTAAGCAGGA TTCTTGCTTC TAATGCAAAA TGTAACCTCC 1380 CTCTATAGGA TGGATAGAGG GATATTAGGT TGAGCACTCA ACACACTGGG 1430
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