Tag | Content |
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EnhancerAtlas ID | HS136-07959 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr17:16132090-16133630 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr17:16132609-16132620 | TTTTATGGCTT | - | 6.62 | NFAT5 | MA0606.1 | chr17:16132962-16132972 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr17:16132962-16132972 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr17:16132962-16132972 | ATTTTCCATT | + | 6.02 | NOTO | MA0710.1 | chr17:16132239-16132249 | GCTAATTAGC | + | 6.02 | NOTO | MA0710.1 | chr17:16132239-16132249 | GCTAATTAGC | - | 6.02 | Pou2f3 | MA0627.1 | chr17:16132239-16132255 | GCTAATTAGCATACTG | - | 6.14 |
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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 |
GH17I016229 | chr17 | 16132921 | 16133130 |
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Enhancer Sequence | AGAAACTCTA TACCTGTTTA GCATTCCTTT TCCCCTCCTC TCCCAAGCCT CTGGTAACCA 60 CCATTCTTTC TATCTCTATG AATTTGTCTA TTCTAGGTAA CTCGAATAAG TGGAATCATA 120 CAATAATTGT TATTTTATGC CTGGCTTATG CTAATTAGCA TACTGTTTTC AAAGTTCATC 180 CATATTGTGG CATGTATCAG AACTTCATTT CTGGTTGAGC TCAGTGGCTC ACACCTGTAA 240 TCCCAGCACT TTGGGAGGCT GAAGTGGAAG GATCCCTTGA GACCAGGAGT TCAAGACCAG 300 TCTGGACAAC ATAGTGAGAT TTCGTCTTTA CAAAAAATAA AAATAAAAAA ATTAGCCAGT 360 CTGGGTGGCG AGTGCCTATA GTCCCAGCTA CTTGGGAGGC TGAAGTGGGA GAATCCCTTG 420 AATCCAGGAG GTCAAGGCTG CAGTAAGCTC TGATCAGTCT GCTGCATTCC GGCCTGGGTG 480 ACAGAGCAAG TCCCTGTCTC AAAAAAAAAC TTCATTTCTT TTTATGGCTT TATTAATATT 540 CCATTGTGTA TATATACATA CATATATATA TGTATGTATA TATACCACAT TTTGTTTATC 600 ATTCATCTAA TGATAGGCAC TTGGGTTATT TCCAATTTGG GGCTATTATG AATAATGCTT 660 CTATGAACAT TGGTGTACAA GTATTTATTT GAGTACCGGT TTTCCTTTTT TTTTTTTTTT 720 TTTTTGAGTA TAATTGCTGA GACATATGGT AATTCTGTAT TTAAATTTTT TGAGAATTGA 780 CAAACTGTTT TCTGCAGCAA CTGTACAGTT TTACGTTGCC ACCAGCAATG AACTATGGTT 840 CCAGTTTCTC CACATCTTTG TCAGCATTTG TAATTTTCCA TTTTTTGGAC TATAGCCATC 900 CTAGTAAGTG TGCAGTGATG ATGTCACATT GTGGTTTTGA TTTTCATTTC CCTGATGACT 960 AAGGATGATG AGCATCTTGC ATCTTTTCAC ATGCTTATTG GCCATCTATA TATCTTCTTT 1020 AGAGAATACC TATTCAAGTC CTTTGCCCAT TTTCTGATTC TAGTTTCATT TTAAAGTCAT 1080 GATTTTTTTT TTTTTTTTTT TTTTGAGACG GAGTCTCGCT CTGTCACCAG GCTGGAGTGC 1140 AGTGGCACGA TCTCAGCTCA CTGCAACCTC CACCTCCTAG GTTCAAGAGA TTCTCCTGCC 1200 TTAACCTCCC GAGTAGCTGG GACTACAGGC GTGTGCCCAC CATGCCCAGC TAATTATTGT 1260 ATTTTTAGTA GAGATGGGGT TTCACTATGT TGGCCAGGAT GGTCTCAATC TCTTGACCTC 1320 GTGATCCACC TGCCTCGGCC TCTCAAAGTG CTGGGATTAC AGGCATGAGG CACTGTGCCT 1380 GGCCAAGTCA TGATTTCTTA GACTGGGTTC TGTGGACACA TCCTAATAGA AGAGGATCTA 1440 GCTCTCTTAG TTTCAGCTTC CTTTGGGAAC CCAGGCCTCT GGGCTCCAGT AACACTGCCT 1500 CCTTCCTTTA CCTTGCCAAC CGAGGGTTGG TAGTCACTTC 1540
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