| Tag | Content |
|---|
EnhancerAtlas ID | HS045-01555 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr1:44029060-44032050 |
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_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 | CAGGGAGGTG TCAAAGAGGC CTCGTACACA TTTGCCTGGC ACTCCGGGGG ACATCTGAAG 60
TTGGAATCTT ACAGGCTGAG AAATAGCAAA TCTCAGGAGG CCAGAGCCAG GACAGAAGGA 120
GCCCCAGGAA CCGACTCTCC ATGTTGGGAG GAGGTTCCTG AGAGACTGGA GGGAAACTGG 180
GAGTGTGTGA GGTCAAGAAA TGCCAAGAGA AAAAAGTGTG CGAAGGAGGA GGAGTGGTCA 240
GCAGGGCGGG GTGCTGCCGA GAGGCCCGGC ATGTGTCCTT AACAGTTAGT TCCGTGGAGC 300
CATTGTTGGC TTTGGTGTTG GGAGACAGCA GGGCTGAGAA GTGAGAGGGA GGCTATCAGT 360
GTCTGTAGTG ACTGGAAGGG CCCGAACCTA GGGAGTGAAT GGATGACAAG AGTCTCCCTG 420
GAGTAGGACT GAGGTTGGGG AGCCACTGAA GGAGAGTCCA GTGTGGGCCC GAGTCTGGAA 480
CTCCAGTGTG GGTCGGGTGT ATGCGCAGGG CATGGCCCCT GGGTTCTTGT GGTGGGGAGG 540
CCTCAACTGG GTTGAGTAGG GCGATGTGGG GTGCCAGGGA AACCCGAGGA AGGAGGGGAT 600
GACTGGGAGG GGGACGCCGT GCCTGCCAAC AGGCCCCAAA CAGCTCAGAT TGAAAAACAA 660
AACAGGCTTT TAAGATGCCA AGTTTGATGA AATCTGAGTG CTGGAAGAGG TGGGAGTTTG 720
CTCTTGGAAA AACAGCTGAA AATCGAGACT CAAAGCTGCG AAGGGAGATG GGCCCAAGGC 780
TCCCCAGGCC CCCCTTACTG CCTGGAAGCC TGGGGGTGGG GCTGGGCTCT CTGGGAGAGT 840
GTGGGAGCGT GCAGATCTGG CAGCCTTCGA CTTTTGGAAG GCGTCTGGCT CTGGCCCTGC 900
TGAGGATGGA GCTGCTGGAG GTGGCCTTGG CTTCTGTGGA GCGGCTGAAG GGCAGGGGGA 960
GCCAGCAGCC CTGCCACCTA CGAGGTTCCT TCATGTGTCT CGTCCCTGCA TGTGTCTCCA 1020
GGCGCACGTG TTTTGGCATA GGTGTGTCTG GCTGTGCATG TCTCCACATG TGTGTTTGCG 1080
TGTCTCTGTG TGCACCGCCT CTGGATCTGC TTGCATGCGC CTGTTTCCAC AGGTGCTAGT 1140
CACTGCAGGT GCCCCTCCAC ATGCACATGT AGGTTTCTAT TTTTACACCT GTCTGTTTCT 1200
CCATGTATAT TTCTGTGGGT TCCTGGCTGT GCATGTTTCT ATGGTGTCTG TGTGTTGAGA 1260
GGCAGGGTGA GGCCAGGCCC AACACTCAAG CTTAGGGGAG GCGGTCAGGC TCACAGACGG 1320
TGCCACCCCA GGGGGCCTGT GTCTGTGTGT GCGGGTGCGT GCCTGCGTTT GCACGGAGAC 1380
GCCACGAAGC TGGGTAAACA TGGGTGAAAA GGTCATACTG ACAGACGGTG CTGCCTGCCC 1440
CAGGACCCTG CAAGGCGTCT CCATCTGTCA GCTTCCCTGG TGCAGCCCCC TCCCTCTGGC 1500
CCAGAGACTC ACCCTCAGGC GTCCAAGGCT GAGCTGGACA AAGAGACCTG TGTGTACTTT 1560
GTAGGGGGCC TCAGCAGCCT CCACCCCCAT CTTAGGCTCC TCTGTCAGGA CCCCAACACA 1620
TGCCCCAGCT CCCACCAGAC TCGCCTTGGT ACTGTCATCC CACCACCTTC CCCCACAACA 1680
GCCTTTACAA AGGCAGTTTT CCCCTCCTCC CTGGAAAGCT TTCTGCCTCC CATGCTCATG 1740
TGTTTCCTGT TCTTGAATCT CCCTCCTCCA GGAAGCCACC AAGATAGCAA GTGAGCTGTG 1800
GAGTCAAACC GATCAGCTCC AACACTGCTG TGGGAGGTTA GCCAAGCGCT CATCCACTTC 1860
TGAACCTTGG ATTCCCACCA TCGACCCCCG ACCCTCCCCT CGCTAGGGCT TGTCATCGTC 1920
TTCTGCCCAT GGGGCAACCA AACCTCTCCA CGGAAGGGGA CAGGTCTCCT TGCTGCAGTG 1980
GGTAAAGGCC AGCGCAGTTA GGTGCAGGAG GCATTCACAC ACACGTGCAC ACTCCCCACC 2040
TTGCACACAT ATCTGCGTGA GCCGGGGAGA CCCTAGGGAA TGTGTGTGCA TGTTGTCTAT 2100
GCATGCGGGT AGAATCCGCA AACGGTGTGG AGACTCGGGC TCTTGGGTAC CTCTGAAGGC 2160
CCCTGAAGTC CCCATGGGCT TCTCCTTCCG TCCAGGGCAC CCTCTTATCA GGCCATGGCC 2220
CTGAGACGCG TAGTGCAGAC GCCCCCGGCG CTGAGGCTGA GGAGGCAGAT GGCCCCTCCC 2280
CGCACTGTGC AGGGCACCCG GTTGGGGGTG GAGGGGAGGG CCGCGTCGGT GAAGCGGGAA 2340
AGCCTAGTGG GAGGATTCCC TGGAGCTGAG GAGCCGGGGC CTGGGAAGGG GCGCAGAGGC 2400
TCCACCCAGG CGGGGGCGGG AAGGGCGGTG CCAGGGCGGA CAGCGGACGC GCGCGCCTGC 2460
ACGGACTCGG GCACACGCAG CCCTTCCGCG GCAGCGCCCG CCGCTCCACC GTCGCCATGG 2520
CTACCGGCTG GCCTGGAGCG GGGAGGGGCC CTTCCTCCCC TTCGGCGCCA ACAGGAGGCG 2580
ATTTGAGGGG ACTCAGCGTG ACTGGTGCAT CCCGGGGTTG GAAAATGGGT GGGTGCTTGC 2640
GACTGTCCAC GTGTGGGGGA CCCTGGGGTT CGCTTTGCGG TAGATGCAAA CGCCGCGGCG 2700
CGTGTGCGGG GCTCTGCAGT GGAGCCTGAG CCGTGCCGGC CGAGGCGTGG TGTGGGGGAG 2760
GCTGCCGGCC CTCTCGCGCG CGGGGTGTTC ACGCCTAGAG CGCTGGGGCT GGGGGCCTAC 2820
CACCCGGTCT CCTCCCAGCC CCACCTCCGA TTTAGCTGTG TGACCTTGGG CAGGTGTCCA 2880
GATGTCTAGA TCTCTCTCAG CCCCTGGTTG CCCATGTACC TCATAAGGGT TTGGTAAAGA 2940
TTTAAGTCAT TTTGTAAAGC ATTTTAACAT AGTACCTGGA ACCTAGTAAA 2990
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