Tag | Content |
---|
EnhancerAtlas ID | HS095-01714 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:112902200-112904000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr1:112903301-112903318 | CAGAACAGAATGTTCCC | - | 6 | Foxd3 | MA0041.1 | chr1:112903597-112903609 | GAATGTTGGTTT | + | 6.04 | NR3C1 | MA0113.3 | chr1:112903301-112903318 | CAGAACAGAATGTTCCC | - | 6.01 | NR3C1 | MA0113.3 | chr1:112903301-112903318 | CAGAACAGAATGTTCCC | + | 6.17 | NR3C2 | MA0727.1 | chr1:112903301-112903318 | CAGAACAGAATGTTCCC | - | 6.1 | NR3C2 | MA0727.1 | chr1:112903301-112903318 | CAGAACAGAATGTTCCC | + | 6.42 | Stat6 | MA0520.1 | chr1:112903910-112903925 | TAGTTCCAGAGAACC | + | 6.05 | ZNF263 | MA0528.1 | chr1:112902263-112902284 | GAGGGAAGGAGGGGGAAAGGG | + | 6.1 | ZNF263 | MA0528.1 | chr1:112902267-112902288 | GAAGGAGGGGGAAAGGGTGGT | + | 6.28 |
|
| 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 |
GH01I112358 | chr1 | 112901501 | 112904228 |
|
Enhancer Sequence | AGTCAACAAA GGGTCGTTGG GCACCTGTAC CACTGTTGAG GCTAAAGAGA GGTGCATCTG 60 TGTGAGGGAA GGAGGGGGAA AGGGTGGTGT TCAGTGATGG AGGAGGGTGG GGTGAGATCT 120 TCAGCATCTA ACAGAGCCAC AAAGAACAGG AAGGGGAAAA GGACACTCCT GTAAAGAGGT 180 CTCTTACTCT CCATCCCTCC TCTCTGCCCA AATACAGATG CTGAGGCCTC AAAGAGGGAG 240 GAGGTGAGGC ATCTTCAAGC CAGGCCCTAC TTCCCCTCCA CTGCTCCAAA CAACCAGGAC 300 CCAACTCTCA CTTGTGCTGG AGGGAAGGGG AGAGAAGAGC TCTGAATCGA GTTTGCAATG 360 AAAGTTTTAA AAATATAAGA GGCTGAGTCT TAATTACTGG AATGAGACTG TTATAGTAAC 420 CGAAAGTGGC TGAAAAGTTA TGGAACCAGA CCAAGATGTC GTTAAGGGAG CGGCTCCTCA 480 GCAGGAAAGA GAGATCTGGC ACAGCACAGC CAGGGCAGTT ACTGGAAGAA ATAAAATCTT 540 TTCATGTTTA TACCCCAACG AGTTGAGACT CCCCAGTGAA TCAGGCACAC AGGAAGTACC 600 TGGGCCTTGG ACACCAGTGT CCCTGTGGTC AGAGTACCCC ATGAAGGATG ATGTCACGCG 660 GAGCACAACC TCCTCTTCCC ATTCAGGTGC TGTCTCACCT CCCAGGGCAA GAGAAGCAGG 720 AGGAATTTGT CCTCCAGCTT TAATGAGGCA CTTAGAAAGA GGAACAGGAT GGTTTCTTCT 780 TACCGGAATC CTCGATGGAA TGCAGGCGCA GGCAGCTGAA AGAGATGGTG CAATTTGCAT 840 ACTTCTGGTG GATTCCAGGA AGCATCAGCC CCATTTCACC CTAACAGCCA GTGGACTCTG 900 CCTGGGAGGG CCAACAGCCA AAGAGAGCTT TCAGTCTCCA GGCTGAGAAA GTCAGGAGAG 960 GAACAAGTCA GGGGACACCA CCAGCCCTGG GACAGCGTGG CAGCATATCC AGAAGATCAG 1020 GAAACTGCCG CAGAGGCTTG GTCCCCTACT GGAAATTGAA AGAAAATGAA GTTTAGAAAG 1080 AGCAGGGTGG GAACTGGTTT GCAGAACAGA ATGTTCCCTT GGCTTATTTT CATCTGGGGG 1140 AAAGGGAAGA ACTAATACTT ATTGAATGCC TGTGCTGTAT CAGGCACTAT GTTCATTCTT 1200 GTCTTATTTA ATCCTCCCAC AACCCTGTAA GGAAAGCATT TTCTCCATTT TACAGATGAA 1260 AAAACTGAGG CAGAGTGGTT GCCTAAGGTC ACATGTTGTT GGAATTTGAA CTTCATGTTT 1320 GTCTGTGTGG TAGACAGACA CAGAGATGCC ATGCTTACAT TGCCCCTTCA ATAAAGGACT 1380 CACTCCCCTG CTACCAAGAA TGTTGGTTTT ATTTGCCCCC AGCAATTAGT TCCTTCAAGG 1440 ACCACCTGAG TTTTTAAGCC ACAGTCACTC TCTTCTTAAG GCAGCCCCTA GCCAATGGCT 1500 GAGCAAGGTG GTAGTACAAA GGCCCATCCC TCTTCTACCA ATGCGGAACT CCTCTAACAA 1560 GCAATTTTTG CTCAGAGCAC CCTGTTAGAC TGGCAGAGGC TTTGTCAAGT CTGCATCAGA 1620 AGCCAAGAGC TCCTCCTGGC CAAACTGCTT CCTCCCTTTT CCACTCACAG GTGATCCTCC 1680 CCTTTGCACT TCTACCTCTG TTGCAGCATC TAGTTCCAGA GAACCCAGTG GAGACTCCTA 1740 ACAGCCTGAC TGCAAAGCTT TCCCTTTTTC TGACACTTTA TCTTCATTTT CACTTGTCCT 1800
|