| Tag | Content |
|---|
EnhancerAtlas ID | HS053-01275 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:44028830-44032070 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr1:44031473-44031484 | GGGCGGGAAGG | + | 6.62 | | RFX1 | MA0509.2 | chr1:44031569-44031585 | CGTCGCCATGGCTACC | + | 6.63 | | RFX1 | MA0509.2 | chr1:44031569-44031585 | CGTCGCCATGGCTACC | - | 6.63 | | RFX2 | MA0600.2 | chr1:44031569-44031585 | CGTCGCCATGGCTACC | + | 6.51 | | RFX2 | MA0600.2 | chr1:44031569-44031585 | CGTCGCCATGGCTACC | - | 6.75 | | Zfx | MA0146.2 | chr1:44031429-44031443 | GGAGCCGGGGCCTG | + | 6.13 |
|
| | Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
| SE_00616 | chr1:44028518-44030367 | Adipose_Nuclei | | SE_00616 | chr1:44031018-44034110 | Adipose_Nuclei | | SE_03403 | chr1:44028960-44031281 | Brain_Angular_Gyrus | | SE_04240 | chr1:44028929-44032553 | Brain_Anterior_Caudate | | SE_05040 | chr1:44028789-44032962 | Brain_Cingulate_Gyrus | | SE_05962 | chr1:44028621-44033904 | Brain_Hippocampus_Middle | | SE_07193 | chr1:44028796-44032406 | Brain_Hippocampus_Middle_150 | | SE_08033 | chr1:44028848-44033378 | Brain_Inferior_Temporal_Lobe | | SE_23829 | chr1:44030959-44031993 | Colon_Crypt_2 | | SE_24870 | chr1:44029728-44030787 | Colon_Crypt_3 | | SE_24870 | chr1:44031008-44032391 | Colon_Crypt_3 | | SE_26649 | chr1:44028759-44032143 | Esophagus | | SE_27645 | chr1:44028997-44029875 | Fetal_Intestine | | SE_27645 | chr1:44031458-44032280 | Fetal_Intestine | | SE_31538 | chr1:44028779-44031982 | Gastric | | SE_33537 | chr1:44028154-44033824 | H2171 | | SE_41575 | chr1:44029231-44029720 | LNCaP | | SE_41575 | chr1:44029923-44031318 | LNCaP | | SE_65452 | chr1:44028737-44032849 | Pancreatic_islets | | SE_69138 | chr1:44029195-44031995 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 44029084 | 44030800 | | chr1 | 44029253 | 44029375 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I043563 | chr1 | 44028826 | 44032589 |
|
Enhancer Sequence | CAAGCGAGAC TCCATCTCAA AAAAAAAAAA AAAAATAAGA TTAGAAAGAG TAGAGGCCTG 60
CCTGGCTACC TGTAGGATTG GGGAGGTGCA AGGCTCCAGG TTCCTGGCTC TGGGGCTGGG 120
TAGGTGGGGG TGCCATTTCT AAGATTCATG TACTAGAGGA GGACCAGGTT TGAGGAGGCG 180
AGTTGGTGAG TCCAGTTAGA AATCTGTTGA GCCAGGTGTG CGCAGGCATC CAGGGAGGTG 240
TCAAAGAGGC CTCGTACACA TTTGCCTGGC ACTCCGGGGG ACATCTGAAG TTGGAATCTT 300
ACAGGCTGAG AAATAGCAAA TCTCAGGAGG CCAGAGCCAG GACAGAAGGA GCCCCAGGAA 360
CCGACTCTCC ATGTTGGGAG GAGGTTCCTG AGAGACTGGA GGGAAACTGG GAGTGTGTGA 420
GGTCAAGAAA TGCCAAGAGA AAAAAGTGTG CGAAGGAGGA GGAGTGGTCA GCAGGGCGGG 480
GTGCTGCCGA GAGGCCCGGC ATGTGTCCTT AACAGTTAGT TCCGTGGAGC CATTGTTGGC 540
TTTGGTGTTG GGAGACAGCA GGGCTGAGAA GTGAGAGGGA GGCTATCAGT GTCTGTAGTG 600
ACTGGAAGGG CCCGAACCTA GGGAGTGAAT GGATGACAAG AGTCTCCCTG GAGTAGGACT 660
GAGGTTGGGG AGCCACTGAA GGAGAGTCCA GTGTGGGCCC GAGTCTGGAA CTCCAGTGTG 720
GGTCGGGTGT ATGCGCAGGG CATGGCCCCT GGGTTCTTGT GGTGGGGAGG CCTCAACTGG 780
GTTGAGTAGG GCGATGTGGG GTGCCAGGGA AACCCGAGGA AGGAGGGGAT GACTGGGAGG 840
GGGACGCCGT GCCTGCCAAC AGGCCCCAAA CAGCTCAGAT TGAAAAACAA AACAGGCTTT 900
TAAGATGCCA AGTTTGATGA AATCTGAGTG CTGGAAGAGG TGGGAGTTTG CTCTTGGAAA 960
AACAGCTGAA AATCGAGACT CAAAGCTGCG AAGGGAGATG GGCCCAAGGC TCCCCAGGCC 1020
CCCCTTACTG CCTGGAAGCC TGGGGGTGGG GCTGGGCTCT CTGGGAGAGT GTGGGAGCGT 1080
GCAGATCTGG CAGCCTTCGA CTTTTGGAAG GCGTCTGGCT CTGGCCCTGC TGAGGATGGA 1140
GCTGCTGGAG GTGGCCTTGG CTTCTGTGGA GCGGCTGAAG GGCAGGGGGA GCCAGCAGCC 1200
CTGCCACCTA CGAGGTTCCT TCATGTGTCT CGTCCCTGCA TGTGTCTCCA GGCGCACGTG 1260
TTTTGGCATA GGTGTGTCTG GCTGTGCATG TCTCCACATG TGTGTTTGCG TGTCTCTGTG 1320
TGCACCGCCT CTGGATCTGC TTGCATGCGC CTGTTTCCAC AGGTGCTAGT CACTGCAGGT 1380
GCCCCTCCAC ATGCACATGT AGGTTTCTAT TTTTACACCT GTCTGTTTCT CCATGTATAT 1440
TTCTGTGGGT TCCTGGCTGT GCATGTTTCT ATGGTGTCTG TGTGTTGAGA GGCAGGGTGA 1500
GGCCAGGCCC AACACTCAAG CTTAGGGGAG GCGGTCAGGC TCACAGACGG TGCCACCCCA 1560
GGGGGCCTGT GTCTGTGTGT GCGGGTGCGT GCCTGCGTTT GCACGGAGAC GCCACGAAGC 1620
TGGGTAAACA TGGGTGAAAA GGTCATACTG ACAGACGGTG CTGCCTGCCC CAGGACCCTG 1680
CAAGGCGTCT CCATCTGTCA GCTTCCCTGG TGCAGCCCCC TCCCTCTGGC CCAGAGACTC 1740
ACCCTCAGGC GTCCAAGGCT GAGCTGGACA AAGAGACCTG TGTGTACTTT GTAGGGGGCC 1800
TCAGCAGCCT CCACCCCCAT CTTAGGCTCC TCTGTCAGGA CCCCAACACA TGCCCCAGCT 1860
CCCACCAGAC TCGCCTTGGT ACTGTCATCC CACCACCTTC CCCCACAACA GCCTTTACAA 1920
AGGCAGTTTT CCCCTCCTCC CTGGAAAGCT TTCTGCCTCC CATGCTCATG TGTTTCCTGT 1980
TCTTGAATCT CCCTCCTCCA GGAAGCCACC AAGATAGCAA GTGAGCTGTG GAGTCAAACC 2040
GATCAGCTCC AACACTGCTG TGGGAGGTTA GCCAAGCGCT CATCCACTTC TGAACCTTGG 2100
ATTCCCACCA TCGACCCCCG ACCCTCCCCT CGCTAGGGCT TGTCATCGTC TTCTGCCCAT 2160
GGGGCAACCA AACCTCTCCA CGGAAGGGGA CAGGTCTCCT TGCTGCAGTG GGTAAAGGCC 2220
AGCGCAGTTA GGTGCAGGAG GCATTCACAC ACACGTGCAC ACTCCCCACC TTGCACACAT 2280
ATCTGCGTGA GCCGGGGAGA CCCTAGGGAA TGTGTGTGCA TGTTGTCTAT GCATGCGGGT 2340
AGAATCCGCA AACGGTGTGG AGACTCGGGC TCTTGGGTAC CTCTGAAGGC CCCTGAAGTC 2400
CCCATGGGCT TCTCCTTCCG TCCAGGGCAC CCTCTTATCA GGCCATGGCC CTGAGACGCG 2460
TAGTGCAGAC GCCCCCGGCG CTGAGGCTGA GGAGGCAGAT GGCCCCTCCC CGCACTGTGC 2520
AGGGCACCCG GTTGGGGGTG GAGGGGAGGG CCGCGTCGGT GAAGCGGGAA AGCCTAGTGG 2580
GAGGATTCCC TGGAGCTGAG GAGCCGGGGC CTGGGAAGGG GCGCAGAGGC TCCACCCAGG 2640
CGGGGGCGGG AAGGGCGGTG CCAGGGCGGA CAGCGGACGC GCGCGCCTGC ACGGACTCGG 2700
GCACACGCAG CCCTTCCGCG GCAGCGCCCG CCGCTCCACC GTCGCCATGG CTACCGGCTG 2760
GCCTGGAGCG GGGAGGGGCC CTTCCTCCCC TTCGGCGCCA ACAGGAGGCG ATTTGAGGGG 2820
ACTCAGCGTG ACTGGTGCAT CCCGGGGTTG GAAAATGGGT GGGTGCTTGC GACTGTCCAC 2880
GTGTGGGGGA CCCTGGGGTT CGCTTTGCGG TAGATGCAAA CGCCGCGGCG CGTGTGCGGG 2940
GCTCTGCAGT GGAGCCTGAG CCGTGCCGGC CGAGGCGTGG TGTGGGGGAG GCTGCCGGCC 3000
CTCTCGCGCG CGGGGTGTTC ACGCCTAGAG CGCTGGGGCT GGGGGCCTAC CACCCGGTCT 3060
CCTCCCAGCC CCACCTCCGA TTTAGCTGTG TGACCTTGGG CAGGTGTCCA GATGTCTAGA 3120
TCTCTCTCAG CCCCTGGTTG CCCATGTACC TCATAAGGGT TTGGTAAAGA TTTAAGTCAT 3180
TTTGTAAAGC ATTTTAACAT AGTACCTGGA ACCTAGTAAA TGCTTCATAA ATCTTACTGT 3240
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