| Tag | Content |
|---|
EnhancerAtlas ID | HS191-01041 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr1:44028890-44031880 |
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 | CCTGGCTACC TGTAGGATTG GGGAGGTGCA AGGCTCCAGG TTCCTGGCTC TGGGGCTGGG 60
TAGGTGGGGG TGCCATTTCT AAGATTCATG TACTAGAGGA GGACCAGGTT TGAGGAGGCG 120
AGTTGGTGAG TCCAGTTAGA AATCTGTTGA GCCAGGTGTG CGCAGGCATC CAGGGAGGTG 180
TCAAAGAGGC CTCGTACACA TTTGCCTGGC ACTCCGGGGG ACATCTGAAG TTGGAATCTT 240
ACAGGCTGAG AAATAGCAAA TCTCAGGAGG CCAGAGCCAG GACAGAAGGA GCCCCAGGAA 300
CCGACTCTCC ATGTTGGGAG GAGGTTCCTG AGAGACTGGA GGGAAACTGG GAGTGTGTGA 360
GGTCAAGAAA TGCCAAGAGA AAAAAGTGTG CGAAGGAGGA GGAGTGGTCA GCAGGGCGGG 420
GTGCTGCCGA GAGGCCCGGC ATGTGTCCTT AACAGTTAGT TCCGTGGAGC CATTGTTGGC 480
TTTGGTGTTG GGAGACAGCA GGGCTGAGAA GTGAGAGGGA GGCTATCAGT GTCTGTAGTG 540
ACTGGAAGGG CCCGAACCTA GGGAGTGAAT GGATGACAAG AGTCTCCCTG GAGTAGGACT 600
GAGGTTGGGG AGCCACTGAA GGAGAGTCCA GTGTGGGCCC GAGTCTGGAA CTCCAGTGTG 660
GGTCGGGTGT ATGCGCAGGG CATGGCCCCT GGGTTCTTGT GGTGGGGAGG CCTCAACTGG 720
GTTGAGTAGG GCGATGTGGG GTGCCAGGGA AACCCGAGGA AGGAGGGGAT GACTGGGAGG 780
GGGACGCCGT GCCTGCCAAC AGGCCCCAAA CAGCTCAGAT TGAAAAACAA AACAGGCTTT 840
TAAGATGCCA AGTTTGATGA AATCTGAGTG CTGGAAGAGG TGGGAGTTTG CTCTTGGAAA 900
AACAGCTGAA AATCGAGACT CAAAGCTGCG AAGGGAGATG GGCCCAAGGC TCCCCAGGCC 960
CCCCTTACTG CCTGGAAGCC TGGGGGTGGG GCTGGGCTCT CTGGGAGAGT GTGGGAGCGT 1020
GCAGATCTGG CAGCCTTCGA CTTTTGGAAG GCGTCTGGCT CTGGCCCTGC TGAGGATGGA 1080
GCTGCTGGAG GTGGCCTTGG CTTCTGTGGA GCGGCTGAAG GGCAGGGGGA GCCAGCAGCC 1140
CTGCCACCTA CGAGGTTCCT TCATGTGTCT CGTCCCTGCA TGTGTCTCCA GGCGCACGTG 1200
TTTTGGCATA GGTGTGTCTG GCTGTGCATG TCTCCACATG TGTGTTTGCG TGTCTCTGTG 1260
TGCACCGCCT CTGGATCTGC TTGCATGCGC CTGTTTCCAC AGGTGCTAGT CACTGCAGGT 1320
GCCCCTCCAC ATGCACATGT AGGTTTCTAT TTTTACACCT GTCTGTTTCT CCATGTATAT 1380
TTCTGTGGGT TCCTGGCTGT GCATGTTTCT ATGGTGTCTG TGTGTTGAGA GGCAGGGTGA 1440
GGCCAGGCCC AACACTCAAG CTTAGGGGAG GCGGTCAGGC TCACAGACGG TGCCACCCCA 1500
GGGGGCCTGT GTCTGTGTGT GCGGGTGCGT GCCTGCGTTT GCACGGAGAC GCCACGAAGC 1560
TGGGTAAACA TGGGTGAAAA GGTCATACTG ACAGACGGTG CTGCCTGCCC CAGGACCCTG 1620
CAAGGCGTCT CCATCTGTCA GCTTCCCTGG TGCAGCCCCC TCCCTCTGGC CCAGAGACTC 1680
ACCCTCAGGC GTCCAAGGCT GAGCTGGACA AAGAGACCTG TGTGTACTTT GTAGGGGGCC 1740
TCAGCAGCCT CCACCCCCAT CTTAGGCTCC TCTGTCAGGA CCCCAACACA TGCCCCAGCT 1800
CCCACCAGAC TCGCCTTGGT ACTGTCATCC CACCACCTTC CCCCACAACA GCCTTTACAA 1860
AGGCAGTTTT CCCCTCCTCC CTGGAAAGCT TTCTGCCTCC CATGCTCATG TGTTTCCTGT 1920
TCTTGAATCT CCCTCCTCCA GGAAGCCACC AAGATAGCAA GTGAGCTGTG GAGTCAAACC 1980
GATCAGCTCC AACACTGCTG TGGGAGGTTA GCCAAGCGCT CATCCACTTC TGAACCTTGG 2040
ATTCCCACCA TCGACCCCCG ACCCTCCCCT CGCTAGGGCT TGTCATCGTC TTCTGCCCAT 2100
GGGGCAACCA AACCTCTCCA CGGAAGGGGA CAGGTCTCCT TGCTGCAGTG GGTAAAGGCC 2160
AGCGCAGTTA GGTGCAGGAG GCATTCACAC ACACGTGCAC ACTCCCCACC TTGCACACAT 2220
ATCTGCGTGA GCCGGGGAGA CCCTAGGGAA TGTGTGTGCA TGTTGTCTAT GCATGCGGGT 2280
AGAATCCGCA AACGGTGTGG AGACTCGGGC TCTTGGGTAC CTCTGAAGGC CCCTGAAGTC 2340
CCCATGGGCT TCTCCTTCCG TCCAGGGCAC CCTCTTATCA GGCCATGGCC CTGAGACGCG 2400
TAGTGCAGAC GCCCCCGGCG CTGAGGCTGA GGAGGCAGAT GGCCCCTCCC CGCACTGTGC 2460
AGGGCACCCG GTTGGGGGTG GAGGGGAGGG CCGCGTCGGT GAAGCGGGAA AGCCTAGTGG 2520
GAGGATTCCC TGGAGCTGAG GAGCCGGGGC CTGGGAAGGG GCGCAGAGGC TCCACCCAGG 2580
CGGGGGCGGG AAGGGCGGTG CCAGGGCGGA CAGCGGACGC GCGCGCCTGC ACGGACTCGG 2640
GCACACGCAG CCCTTCCGCG GCAGCGCCCG CCGCTCCACC GTCGCCATGG CTACCGGCTG 2700
GCCTGGAGCG GGGAGGGGCC CTTCCTCCCC TTCGGCGCCA ACAGGAGGCG ATTTGAGGGG 2760
ACTCAGCGTG ACTGGTGCAT CCCGGGGTTG GAAAATGGGT GGGTGCTTGC GACTGTCCAC 2820
GTGTGGGGGA CCCTGGGGTT CGCTTTGCGG TAGATGCAAA CGCCGCGGCG CGTGTGCGGG 2880
GCTCTGCAGT GGAGCCTGAG CCGTGCCGGC CGAGGCGTGG TGTGGGGGAG GCTGCCGGCC 2940
CTCTCGCGCG CGGGGTGTTC ACGCCTAGAG CGCTGGGGCT GGGGGCCTAC 2990
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