| Tag | Content |
|---|
EnhancerAtlas ID | HS080-00988 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:44028970-44032020 |
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 | AAGATTCATG TACTAGAGGA GGACCAGGTT TGAGGAGGCG AGTTGGTGAG TCCAGTTAGA 60
AATCTGTTGA GCCAGGTGTG CGCAGGCATC CAGGGAGGTG TCAAAGAGGC CTCGTACACA 120
TTTGCCTGGC ACTCCGGGGG ACATCTGAAG TTGGAATCTT ACAGGCTGAG AAATAGCAAA 180
TCTCAGGAGG CCAGAGCCAG GACAGAAGGA GCCCCAGGAA CCGACTCTCC ATGTTGGGAG 240
GAGGTTCCTG AGAGACTGGA GGGAAACTGG GAGTGTGTGA GGTCAAGAAA TGCCAAGAGA 300
AAAAAGTGTG CGAAGGAGGA GGAGTGGTCA GCAGGGCGGG GTGCTGCCGA GAGGCCCGGC 360
ATGTGTCCTT AACAGTTAGT TCCGTGGAGC CATTGTTGGC TTTGGTGTTG GGAGACAGCA 420
GGGCTGAGAA GTGAGAGGGA GGCTATCAGT GTCTGTAGTG ACTGGAAGGG CCCGAACCTA 480
GGGAGTGAAT GGATGACAAG AGTCTCCCTG GAGTAGGACT GAGGTTGGGG AGCCACTGAA 540
GGAGAGTCCA GTGTGGGCCC GAGTCTGGAA CTCCAGTGTG GGTCGGGTGT ATGCGCAGGG 600
CATGGCCCCT GGGTTCTTGT GGTGGGGAGG CCTCAACTGG GTTGAGTAGG GCGATGTGGG 660
GTGCCAGGGA AACCCGAGGA AGGAGGGGAT GACTGGGAGG GGGACGCCGT GCCTGCCAAC 720
AGGCCCCAAA CAGCTCAGAT TGAAAAACAA AACAGGCTTT TAAGATGCCA AGTTTGATGA 780
AATCTGAGTG CTGGAAGAGG TGGGAGTTTG CTCTTGGAAA AACAGCTGAA AATCGAGACT 840
CAAAGCTGCG AAGGGAGATG GGCCCAAGGC TCCCCAGGCC CCCCTTACTG CCTGGAAGCC 900
TGGGGGTGGG GCTGGGCTCT CTGGGAGAGT GTGGGAGCGT GCAGATCTGG CAGCCTTCGA 960
CTTTTGGAAG GCGTCTGGCT CTGGCCCTGC TGAGGATGGA GCTGCTGGAG GTGGCCTTGG 1020
CTTCTGTGGA GCGGCTGAAG GGCAGGGGGA GCCAGCAGCC CTGCCACCTA CGAGGTTCCT 1080
TCATGTGTCT CGTCCCTGCA TGTGTCTCCA GGCGCACGTG TTTTGGCATA GGTGTGTCTG 1140
GCTGTGCATG TCTCCACATG TGTGTTTGCG TGTCTCTGTG TGCACCGCCT CTGGATCTGC 1200
TTGCATGCGC CTGTTTCCAC AGGTGCTAGT CACTGCAGGT GCCCCTCCAC ATGCACATGT 1260
AGGTTTCTAT TTTTACACCT GTCTGTTTCT CCATGTATAT TTCTGTGGGT TCCTGGCTGT 1320
GCATGTTTCT ATGGTGTCTG TGTGTTGAGA GGCAGGGTGA GGCCAGGCCC AACACTCAAG 1380
CTTAGGGGAG GCGGTCAGGC TCACAGACGG TGCCACCCCA GGGGGCCTGT GTCTGTGTGT 1440
GCGGGTGCGT GCCTGCGTTT GCACGGAGAC GCCACGAAGC TGGGTAAACA TGGGTGAAAA 1500
GGTCATACTG ACAGACGGTG CTGCCTGCCC CAGGACCCTG CAAGGCGTCT CCATCTGTCA 1560
GCTTCCCTGG TGCAGCCCCC TCCCTCTGGC CCAGAGACTC ACCCTCAGGC GTCCAAGGCT 1620
GAGCTGGACA AAGAGACCTG TGTGTACTTT GTAGGGGGCC TCAGCAGCCT CCACCCCCAT 1680
CTTAGGCTCC TCTGTCAGGA CCCCAACACA TGCCCCAGCT CCCACCAGAC TCGCCTTGGT 1740
ACTGTCATCC CACCACCTTC CCCCACAACA GCCTTTACAA AGGCAGTTTT CCCCTCCTCC 1800
CTGGAAAGCT TTCTGCCTCC CATGCTCATG TGTTTCCTGT TCTTGAATCT CCCTCCTCCA 1860
GGAAGCCACC AAGATAGCAA GTGAGCTGTG GAGTCAAACC GATCAGCTCC AACACTGCTG 1920
TGGGAGGTTA GCCAAGCGCT CATCCACTTC TGAACCTTGG ATTCCCACCA TCGACCCCCG 1980
ACCCTCCCCT CGCTAGGGCT TGTCATCGTC TTCTGCCCAT GGGGCAACCA AACCTCTCCA 2040
CGGAAGGGGA CAGGTCTCCT TGCTGCAGTG GGTAAAGGCC AGCGCAGTTA GGTGCAGGAG 2100
GCATTCACAC ACACGTGCAC ACTCCCCACC TTGCACACAT ATCTGCGTGA GCCGGGGAGA 2160
CCCTAGGGAA TGTGTGTGCA TGTTGTCTAT GCATGCGGGT AGAATCCGCA AACGGTGTGG 2220
AGACTCGGGC TCTTGGGTAC CTCTGAAGGC CCCTGAAGTC CCCATGGGCT TCTCCTTCCG 2280
TCCAGGGCAC CCTCTTATCA GGCCATGGCC CTGAGACGCG TAGTGCAGAC GCCCCCGGCG 2340
CTGAGGCTGA GGAGGCAGAT GGCCCCTCCC CGCACTGTGC AGGGCACCCG GTTGGGGGTG 2400
GAGGGGAGGG CCGCGTCGGT GAAGCGGGAA AGCCTAGTGG GAGGATTCCC TGGAGCTGAG 2460
GAGCCGGGGC CTGGGAAGGG GCGCAGAGGC TCCACCCAGG CGGGGGCGGG AAGGGCGGTG 2520
CCAGGGCGGA CAGCGGACGC GCGCGCCTGC ACGGACTCGG GCACACGCAG CCCTTCCGCG 2580
GCAGCGCCCG CCGCTCCACC GTCGCCATGG CTACCGGCTG GCCTGGAGCG GGGAGGGGCC 2640
CTTCCTCCCC TTCGGCGCCA ACAGGAGGCG ATTTGAGGGG ACTCAGCGTG ACTGGTGCAT 2700
CCCGGGGTTG GAAAATGGGT GGGTGCTTGC GACTGTCCAC GTGTGGGGGA CCCTGGGGTT 2760
CGCTTTGCGG TAGATGCAAA CGCCGCGGCG CGTGTGCGGG GCTCTGCAGT GGAGCCTGAG 2820
CCGTGCCGGC CGAGGCGTGG TGTGGGGGAG GCTGCCGGCC CTCTCGCGCG CGGGGTGTTC 2880
ACGCCTAGAG CGCTGGGGCT GGGGGCCTAC CACCCGGTCT CCTCCCAGCC CCACCTCCGA 2940
TTTAGCTGTG TGACCTTGGG CAGGTGTCCA GATGTCTAGA TCTCTCTCAG CCCCTGGTTG 3000
CCCATGTACC TCATAAGGGT TTGGTAAAGA TTTAAGTCAT TTTGTAAAGC 3050
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