| Tag | Content |
|---|
EnhancerAtlas ID | HS156-00425 |
Organism | Homo sapiens |
Tissue/cell | P493-6 |
Coordinate | chr1:44028960-44031620 |
SNPs | | Number: 1 | 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_08920 | chr1:44030094-44030379 | Brain_Mid_Frontal_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_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 | TGCCATTTCT AAGATTCATG TACTAGAGGA GGACCAGGTT TGAGGAGGCG AGTTGGTGAG 60
TCCAGTTAGA AATCTGTTGA GCCAGGTGTG CGCAGGCATC CAGGGAGGTG TCAAAGAGGC 120
CTCGTACACA TTTGCCTGGC ACTCCGGGGG ACATCTGAAG TTGGAATCTT ACAGGCTGAG 180
AAATAGCAAA TCTCAGGAGG CCAGAGCCAG GACAGAAGGA GCCCCAGGAA CCGACTCTCC 240
ATGTTGGGAG GAGGTTCCTG AGAGACTGGA GGGAAACTGG GAGTGTGTGA GGTCAAGAAA 300
TGCCAAGAGA AAAAAGTGTG CGAAGGAGGA GGAGTGGTCA GCAGGGCGGG GTGCTGCCGA 360
GAGGCCCGGC ATGTGTCCTT AACAGTTAGT TCCGTGGAGC CATTGTTGGC TTTGGTGTTG 420
GGAGACAGCA GGGCTGAGAA GTGAGAGGGA GGCTATCAGT GTCTGTAGTG ACTGGAAGGG 480
CCCGAACCTA GGGAGTGAAT GGATGACAAG AGTCTCCCTG GAGTAGGACT GAGGTTGGGG 540
AGCCACTGAA GGAGAGTCCA GTGTGGGCCC GAGTCTGGAA CTCCAGTGTG GGTCGGGTGT 600
ATGCGCAGGG CATGGCCCCT GGGTTCTTGT GGTGGGGAGG CCTCAACTGG GTTGAGTAGG 660
GCGATGTGGG GTGCCAGGGA AACCCGAGGA AGGAGGGGAT GACTGGGAGG GGGACGCCGT 720
GCCTGCCAAC AGGCCCCAAA CAGCTCAGAT TGAAAAACAA AACAGGCTTT TAAGATGCCA 780
AGTTTGATGA AATCTGAGTG CTGGAAGAGG TGGGAGTTTG CTCTTGGAAA AACAGCTGAA 840
AATCGAGACT CAAAGCTGCG AAGGGAGATG GGCCCAAGGC TCCCCAGGCC CCCCTTACTG 900
CCTGGAAGCC TGGGGGTGGG GCTGGGCTCT CTGGGAGAGT GTGGGAGCGT GCAGATCTGG 960
CAGCCTTCGA CTTTTGGAAG GCGTCTGGCT CTGGCCCTGC TGAGGATGGA GCTGCTGGAG 1020
GTGGCCTTGG CTTCTGTGGA GCGGCTGAAG GGCAGGGGGA GCCAGCAGCC CTGCCACCTA 1080
CGAGGTTCCT TCATGTGTCT CGTCCCTGCA TGTGTCTCCA GGCGCACGTG TTTTGGCATA 1140
GGTGTGTCTG GCTGTGCATG TCTCCACATG TGTGTTTGCG TGTCTCTGTG TGCACCGCCT 1200
CTGGATCTGC TTGCATGCGC CTGTTTCCAC AGGTGCTAGT CACTGCAGGT GCCCCTCCAC 1260
ATGCACATGT AGGTTTCTAT TTTTACACCT GTCTGTTTCT CCATGTATAT TTCTGTGGGT 1320
TCCTGGCTGT GCATGTTTCT ATGGTGTCTG TGTGTTGAGA GGCAGGGTGA GGCCAGGCCC 1380
AACACTCAAG CTTAGGGGAG GCGGTCAGGC TCACAGACGG TGCCACCCCA GGGGGCCTGT 1440
GTCTGTGTGT GCGGGTGCGT GCCTGCGTTT GCACGGAGAC GCCACGAAGC TGGGTAAACA 1500
TGGGTGAAAA GGTCATACTG ACAGACGGTG CTGCCTGCCC CAGGACCCTG CAAGGCGTCT 1560
CCATCTGTCA GCTTCCCTGG TGCAGCCCCC TCCCTCTGGC CCAGAGACTC ACCCTCAGGC 1620
GTCCAAGGCT GAGCTGGACA AAGAGACCTG TGTGTACTTT GTAGGGGGCC TCAGCAGCCT 1680
CCACCCCCAT CTTAGGCTCC TCTGTCAGGA CCCCAACACA TGCCCCAGCT CCCACCAGAC 1740
TCGCCTTGGT ACTGTCATCC CACCACCTTC CCCCACAACA GCCTTTACAA AGGCAGTTTT 1800
CCCCTCCTCC CTGGAAAGCT TTCTGCCTCC CATGCTCATG TGTTTCCTGT TCTTGAATCT 1860
CCCTCCTCCA GGAAGCCACC AAGATAGCAA GTGAGCTGTG GAGTCAAACC GATCAGCTCC 1920
AACACTGCTG TGGGAGGTTA GCCAAGCGCT CATCCACTTC TGAACCTTGG ATTCCCACCA 1980
TCGACCCCCG ACCCTCCCCT CGCTAGGGCT TGTCATCGTC TTCTGCCCAT GGGGCAACCA 2040
AACCTCTCCA CGGAAGGGGA CAGGTCTCCT TGCTGCAGTG GGTAAAGGCC AGCGCAGTTA 2100
GGTGCAGGAG GCATTCACAC ACACGTGCAC ACTCCCCACC TTGCACACAT ATCTGCGTGA 2160
GCCGGGGAGA CCCTAGGGAA TGTGTGTGCA TGTTGTCTAT GCATGCGGGT AGAATCCGCA 2220
AACGGTGTGG AGACTCGGGC TCTTGGGTAC CTCTGAAGGC CCCTGAAGTC CCCATGGGCT 2280
TCTCCTTCCG TCCAGGGCAC CCTCTTATCA GGCCATGGCC CTGAGACGCG TAGTGCAGAC 2340
GCCCCCGGCG CTGAGGCTGA GGAGGCAGAT GGCCCCTCCC CGCACTGTGC AGGGCACCCG 2400
GTTGGGGGTG GAGGGGAGGG CCGCGTCGGT GAAGCGGGAA AGCCTAGTGG GAGGATTCCC 2460
TGGAGCTGAG GAGCCGGGGC CTGGGAAGGG GCGCAGAGGC TCCACCCAGG CGGGGGCGGG 2520
AAGGGCGGTG CCAGGGCGGA CAGCGGACGC GCGCGCCTGC ACGGACTCGG GCACACGCAG 2580
CCCTTCCGCG GCAGCGCCCG CCGCTCCACC GTCGCCATGG CTACCGGCTG GCCTGGAGCG 2640
GGGAGGGGCC CTTCCTCCCC 2660
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