| Tag | Content |
|---|
EnhancerAtlas ID | HS130-02820 |
Organism | Homo sapiens |
Tissue/cell | MDA-MB-231 |
Coordinate | chr1:224355860-224358020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr1:224356699-224356710 | CATGAGTCACC | - | 6.62 | | IRF1 | MA0050.2 | chr1:224357855-224357876 | TGTTGCTTTCTTTTTCTTTTT | + | 7.23 | | JUND | MA0491.1 | chr1:224356699-224356710 | CATGAGTCACC | - | 6.02 | | Lhx3 | MA0135.1 | chr1:224355863-224355876 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr1:224355867-224355880 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr1:224355871-224355884 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr1:224355860-224355873 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr1:224355864-224355877 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr1:224355868-224355881 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr1:224355872-224355885 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr1:224355875-224355888 | TAATTAATTAAAT | + | 6 | | Nr2f6(var.2) | MA0728.1 | chr1:224356381-224356396 | CGAACTCTTGACCTT | - | 6.06 | | POU6F1 | MA0628.1 | chr1:224355861-224355871 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr1:224355865-224355875 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr1:224355869-224355879 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr1:224355873-224355883 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr1:224355861-224355871 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr1:224355865-224355875 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr1:224355869-224355879 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr1:224355873-224355883 | ATTAATTAAT | - | 6.02 | | ZNF263 | MA0528.1 | chr1:224357678-224357699 | TTTTCCTCCTCCCCCTCCTGC | - | 6.14 | | ZNF263 | MA0528.1 | chr1:224357634-224357655 | GGAGAAGGGCAGGAAGGAGGA | + | 6.85 | | ZNF263 | MA0528.1 | chr1:224357669-224357690 | TCTCTTTGCTTTTCCTCCTCC | - | 6.87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 224357505 | 224357898 | | chr1 | 224356788 | 224356993 | | chr1 | 224357572 | 224357970 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I224168 | chr1 | 224356104 | 224359018 |
|
Enhancer Sequence | AATTAATTAA TTAATTAATT AATTAAATAA AAGGGACCTC AGAAAACTCC TTCACCTCTT 60
CTGCCATGTG AGGTTATAGC CAGAAGACGG CCATCCACGA ACAAGGAAGC AGCCCCTCAC 120
CAGATACTGA ATATGCCAGT GCCTTGATCT TGGACTTCCC AGGCTCCAGA ATTTTTTTTT 180
TTTTTTTTTG AGACGGAGTC TCTGTCACCC AGGCGGGAGT GCAATGGCAC GATCTGGGCT 240
CACTGCAACC TCTACCTCCC GAGTTCAAGC GATTCTCCCA CCTCAGCCTC CCGAGTAGCT 300
GGGATTACAG GCATGCGCCA CCATACCTGG CTAATTTTGT ATTTTTAGTA GAGATGAGGT 360
TTCTCCATGT TGCTCAGGTT GGTCTCAAAC TCCCGACCTC AGGTGATCCA CCCACCTCAG 420
CCTCCCAAAG TGCTGGGATT ACAGGGGTGA GCCACCACGC CCAGCCTAAT TTTTGTATTC 480
TTAGTAGAGA CGGGTTTTCA CCATGTTGGC CAGGCTGGTT TCGAACTCTT GACCTTGTGA 540
TCCATCCGCT TTGGCCTCCC AAAGTGCTGG GATTATAGGC GTGAGCTACT GTGCCTGGCC 600
AGACTGTTTT CTTAAAAACC AAAAGCCTGG GAAGAAAAAC AAAATATCTT GCAAATGTAT 660
TCTCAATCCC AGTCAATCCC CTGCAAAACT CAGACTCTGG AAGAATGAAA GCTATGCGCT 720
CTTTTCTCCA CTCATTCATA TTGTTGGCTT CACACAGATA GAAAAAGCTA CTTCATCCTG 780
CAGAACTGCT CTATCAGTTC ATGGTGTTTT CCTGGATCCT GGACCCCTGC CTTCCCCACC 840
ATGAGTCACC TCTGGATCGA GTCCATCTTC TATTTGGGAT TTGGAACCAG ACAACCTTTG 900
TCCCTTTTTA GCCTCTGCTG CACTCTAAGC TGTGTGATCT AAGACACGTC ACTCACATTC 960
TGGAAGTATT CGCTTCCTCA TACATGAAAT GGGGGAAATT TCTCTAACCA TAAGCCTGCG 1020
GTTTTGATTT CAGTGCTCAC TAGTTCAAGA CTTTTCTTCT TGCCTATGCC CCTTCACCCT 1080
CTTCCTTTGT CAATTTCCTT TTTCATAAGC TGTGGCTGCT GGTGAGTAAA ATAGTCATCT 1140
GAGTACAACT GCTTTTGCAT GAGCTAGACT TGGAAGGGTG CAAATGGAAG CAGATTCATT 1200
TCTTCTCAGT AACTGCTCTT TTAGACTGTC CTGTTGCATT GTTCTGCCCT GATCCCAGAA 1260
GGAATCTCAG GCAGATCCCA GAGCCTTGTA GACTCTCCTG GTCACTAACA AATTAATCAC 1320
CTTTATCCAG TTATTAAAAA ATCCAGCCCG ATCCGAAGAA AGACTTTATT GTCTCAATTG 1380
ATTAAAGCTT CTTTCCTCTT TTTTTTCTCT TTTTTTGAGA CGGAGTCTTG CTCTGTCGCA 1440
CAGGCTGGAG TGCAGTGGTG CGATCTTGGC TCACTGCAGC CTCCACCTCC CGGGTTCAAG 1500
CGATTTTCCT GCCTCAGCCT CCCAAGTAGC TGGGATTACA GGTGCCTGCC ACCAAGCCCA 1560
GCTAATTTTT GCATTTTTAG TAGAGACGGG GTTTCGCCAT GTTGGACAGG CTGGTCTTGA 1620
ACTGCTGACC TCAGGTGATC TGCCTGCCTT GGCCTCCCAA AATTCTGGGA TTACAGGCAT 1680
GAGCCACTGT GCCCTCCCGC TTCTTTCTTC TTTCTGTAAG TCAGGCCTGA GTTGGACTTC 1740
GGAGAAGCTT TGAGTTGGGC TTCTCCTTTT CAGTGGAGAA GGGCAGGAAG GAGGATGTCT 1800
TCCATTTATT CTCTTTGCTT TTCCTCCTCC CCCTCCTGCA AGACTCTCTG CTGTCTAACT 1860
CAGTGGGGAG GAGAGACAGA ATAAAGAAAA AAAATCTGCA TTACTGGTAT GGTTGGAATC 1920
TGTCATGTGT GTCTCTTGGT TGAGGCAGAG ATCACACTTT GGGGCTGTTT TCCCCAAGGC 1980
ATTTTCCACT GTTGTTGTTG CTTTCTTTTT CTTTTTTTAA GAGATAAGGT CTTGCCCTAT 2040
CACTCACTAC AGTCTTGAAC TCCTGAGCTC AAGTGATCCT CCTGCCTCAG CTTACTGAGT 2100
AGCTGGGACT ACCATGCCTG GCTAATTATT TTTATTTTTG ATAGATGCAG AGTCTTGCTA 2160
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