| Tag | Content |
|---|
EnhancerAtlas ID | HS030-00839 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr1:44028820-44031970 |
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 | CCTAGGCGAC CAAGCGAGAC TCCATCTCAA AAAAAAAAAA AAAAATAAGA TTAGAAAGAG 60
TAGAGGCCTG CCTGGCTACC TGTAGGATTG GGGAGGTGCA AGGCTCCAGG TTCCTGGCTC 120
TGGGGCTGGG TAGGTGGGGG TGCCATTTCT AAGATTCATG TACTAGAGGA GGACCAGGTT 180
TGAGGAGGCG AGTTGGTGAG TCCAGTTAGA AATCTGTTGA GCCAGGTGTG CGCAGGCATC 240
CAGGGAGGTG TCAAAGAGGC CTCGTACACA TTTGCCTGGC ACTCCGGGGG ACATCTGAAG 300
TTGGAATCTT ACAGGCTGAG AAATAGCAAA TCTCAGGAGG CCAGAGCCAG GACAGAAGGA 360
GCCCCAGGAA CCGACTCTCC ATGTTGGGAG GAGGTTCCTG AGAGACTGGA GGGAAACTGG 420
GAGTGTGTGA GGTCAAGAAA TGCCAAGAGA AAAAAGTGTG CGAAGGAGGA GGAGTGGTCA 480
GCAGGGCGGG GTGCTGCCGA GAGGCCCGGC ATGTGTCCTT AACAGTTAGT TCCGTGGAGC 540
CATTGTTGGC TTTGGTGTTG GGAGACAGCA GGGCTGAGAA GTGAGAGGGA GGCTATCAGT 600
GTCTGTAGTG ACTGGAAGGG CCCGAACCTA GGGAGTGAAT GGATGACAAG AGTCTCCCTG 660
GAGTAGGACT GAGGTTGGGG AGCCACTGAA GGAGAGTCCA GTGTGGGCCC GAGTCTGGAA 720
CTCCAGTGTG GGTCGGGTGT ATGCGCAGGG CATGGCCCCT GGGTTCTTGT GGTGGGGAGG 780
CCTCAACTGG GTTGAGTAGG GCGATGTGGG GTGCCAGGGA AACCCGAGGA AGGAGGGGAT 840
GACTGGGAGG GGGACGCCGT GCCTGCCAAC AGGCCCCAAA CAGCTCAGAT TGAAAAACAA 900
AACAGGCTTT TAAGATGCCA AGTTTGATGA AATCTGAGTG CTGGAAGAGG TGGGAGTTTG 960
CTCTTGGAAA AACAGCTGAA AATCGAGACT CAAAGCTGCG AAGGGAGATG GGCCCAAGGC 1020
TCCCCAGGCC CCCCTTACTG CCTGGAAGCC TGGGGGTGGG GCTGGGCTCT CTGGGAGAGT 1080
GTGGGAGCGT GCAGATCTGG CAGCCTTCGA CTTTTGGAAG GCGTCTGGCT CTGGCCCTGC 1140
TGAGGATGGA GCTGCTGGAG GTGGCCTTGG CTTCTGTGGA GCGGCTGAAG GGCAGGGGGA 1200
GCCAGCAGCC CTGCCACCTA CGAGGTTCCT TCATGTGTCT CGTCCCTGCA TGTGTCTCCA 1260
GGCGCACGTG TTTTGGCATA GGTGTGTCTG GCTGTGCATG TCTCCACATG TGTGTTTGCG 1320
TGTCTCTGTG TGCACCGCCT CTGGATCTGC TTGCATGCGC CTGTTTCCAC AGGTGCTAGT 1380
CACTGCAGGT GCCCCTCCAC ATGCACATGT AGGTTTCTAT TTTTACACCT GTCTGTTTCT 1440
CCATGTATAT TTCTGTGGGT TCCTGGCTGT GCATGTTTCT ATGGTGTCTG TGTGTTGAGA 1500
GGCAGGGTGA GGCCAGGCCC AACACTCAAG CTTAGGGGAG GCGGTCAGGC TCACAGACGG 1560
TGCCACCCCA GGGGGCCTGT GTCTGTGTGT GCGGGTGCGT GCCTGCGTTT GCACGGAGAC 1620
GCCACGAAGC TGGGTAAACA TGGGTGAAAA GGTCATACTG ACAGACGGTG CTGCCTGCCC 1680
CAGGACCCTG CAAGGCGTCT CCATCTGTCA GCTTCCCTGG TGCAGCCCCC TCCCTCTGGC 1740
CCAGAGACTC ACCCTCAGGC GTCCAAGGCT GAGCTGGACA AAGAGACCTG TGTGTACTTT 1800
GTAGGGGGCC TCAGCAGCCT CCACCCCCAT CTTAGGCTCC TCTGTCAGGA CCCCAACACA 1860
TGCCCCAGCT CCCACCAGAC TCGCCTTGGT ACTGTCATCC CACCACCTTC CCCCACAACA 1920
GCCTTTACAA AGGCAGTTTT CCCCTCCTCC CTGGAAAGCT TTCTGCCTCC CATGCTCATG 1980
TGTTTCCTGT TCTTGAATCT CCCTCCTCCA GGAAGCCACC AAGATAGCAA GTGAGCTGTG 2040
GAGTCAAACC GATCAGCTCC AACACTGCTG TGGGAGGTTA GCCAAGCGCT CATCCACTTC 2100
TGAACCTTGG ATTCCCACCA TCGACCCCCG ACCCTCCCCT CGCTAGGGCT TGTCATCGTC 2160
TTCTGCCCAT GGGGCAACCA AACCTCTCCA CGGAAGGGGA CAGGTCTCCT TGCTGCAGTG 2220
GGTAAAGGCC AGCGCAGTTA GGTGCAGGAG GCATTCACAC ACACGTGCAC ACTCCCCACC 2280
TTGCACACAT ATCTGCGTGA GCCGGGGAGA CCCTAGGGAA TGTGTGTGCA TGTTGTCTAT 2340
GCATGCGGGT AGAATCCGCA AACGGTGTGG AGACTCGGGC TCTTGGGTAC CTCTGAAGGC 2400
CCCTGAAGTC CCCATGGGCT TCTCCTTCCG TCCAGGGCAC CCTCTTATCA GGCCATGGCC 2460
CTGAGACGCG TAGTGCAGAC GCCCCCGGCG CTGAGGCTGA GGAGGCAGAT GGCCCCTCCC 2520
CGCACTGTGC AGGGCACCCG GTTGGGGGTG GAGGGGAGGG CCGCGTCGGT GAAGCGGGAA 2580
AGCCTAGTGG GAGGATTCCC TGGAGCTGAG GAGCCGGGGC CTGGGAAGGG GCGCAGAGGC 2640
TCCACCCAGG CGGGGGCGGG AAGGGCGGTG CCAGGGCGGA CAGCGGACGC GCGCGCCTGC 2700
ACGGACTCGG GCACACGCAG CCCTTCCGCG GCAGCGCCCG CCGCTCCACC GTCGCCATGG 2760
CTACCGGCTG GCCTGGAGCG GGGAGGGGCC CTTCCTCCCC TTCGGCGCCA ACAGGAGGCG 2820
ATTTGAGGGG ACTCAGCGTG ACTGGTGCAT CCCGGGGTTG GAAAATGGGT GGGTGCTTGC 2880
GACTGTCCAC GTGTGGGGGA CCCTGGGGTT CGCTTTGCGG TAGATGCAAA CGCCGCGGCG 2940
CGTGTGCGGG GCTCTGCAGT GGAGCCTGAG CCGTGCCGGC CGAGGCGTGG TGTGGGGGAG 3000
GCTGCCGGCC CTCTCGCGCG CGGGGTGTTC ACGCCTAGAG CGCTGGGGCT GGGGGCCTAC 3060
CACCCGGTCT CCTCCCAGCC CCACCTCCGA TTTAGCTGTG TGACCTTGGG CAGGTGTCCA 3120
GATGTCTAGA TCTCTCTCAG CCCCTGGTTG 3150
|
