| Tag | Content |
|---|
EnhancerAtlas ID | HS182-00826 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:44029100-44031900 |
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: 21 | 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_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: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I043563 | chr1 | 44028826 | 44032589 |
|
Enhancer Sequence | ACTCCGGGGG ACATCTGAAG TTGGAATCTT ACAGGCTGAG AAATAGCAAA TCTCAGGAGG 60
CCAGAGCCAG GACAGAAGGA GCCCCAGGAA CCGACTCTCC ATGTTGGGAG GAGGTTCCTG 120
AGAGACTGGA GGGAAACTGG GAGTGTGTGA GGTCAAGAAA TGCCAAGAGA AAAAAGTGTG 180
CGAAGGAGGA GGAGTGGTCA GCAGGGCGGG GTGCTGCCGA GAGGCCCGGC ATGTGTCCTT 240
AACAGTTAGT TCCGTGGAGC CATTGTTGGC TTTGGTGTTG GGAGACAGCA GGGCTGAGAA 300
GTGAGAGGGA GGCTATCAGT GTCTGTAGTG ACTGGAAGGG CCCGAACCTA GGGAGTGAAT 360
GGATGACAAG AGTCTCCCTG GAGTAGGACT GAGGTTGGGG AGCCACTGAA GGAGAGTCCA 420
GTGTGGGCCC GAGTCTGGAA CTCCAGTGTG GGTCGGGTGT ATGCGCAGGG CATGGCCCCT 480
GGGTTCTTGT GGTGGGGAGG CCTCAACTGG GTTGAGTAGG GCGATGTGGG GTGCCAGGGA 540
AACCCGAGGA AGGAGGGGAT GACTGGGAGG GGGACGCCGT GCCTGCCAAC AGGCCCCAAA 600
CAGCTCAGAT TGAAAAACAA AACAGGCTTT TAAGATGCCA AGTTTGATGA AATCTGAGTG 660
CTGGAAGAGG TGGGAGTTTG CTCTTGGAAA AACAGCTGAA AATCGAGACT CAAAGCTGCG 720
AAGGGAGATG GGCCCAAGGC TCCCCAGGCC CCCCTTACTG CCTGGAAGCC TGGGGGTGGG 780
GCTGGGCTCT CTGGGAGAGT GTGGGAGCGT GCAGATCTGG CAGCCTTCGA CTTTTGGAAG 840
GCGTCTGGCT CTGGCCCTGC TGAGGATGGA GCTGCTGGAG GTGGCCTTGG CTTCTGTGGA 900
GCGGCTGAAG GGCAGGGGGA GCCAGCAGCC CTGCCACCTA CGAGGTTCCT TCATGTGTCT 960
CGTCCCTGCA TGTGTCTCCA GGCGCACGTG TTTTGGCATA GGTGTGTCTG GCTGTGCATG 1020
TCTCCACATG TGTGTTTGCG TGTCTCTGTG TGCACCGCCT CTGGATCTGC TTGCATGCGC 1080
CTGTTTCCAC AGGTGCTAGT CACTGCAGGT GCCCCTCCAC ATGCACATGT AGGTTTCTAT 1140
TTTTACACCT GTCTGTTTCT CCATGTATAT TTCTGTGGGT TCCTGGCTGT GCATGTTTCT 1200
ATGGTGTCTG TGTGTTGAGA GGCAGGGTGA GGCCAGGCCC AACACTCAAG CTTAGGGGAG 1260
GCGGTCAGGC TCACAGACGG TGCCACCCCA GGGGGCCTGT GTCTGTGTGT GCGGGTGCGT 1320
GCCTGCGTTT GCACGGAGAC GCCACGAAGC TGGGTAAACA TGGGTGAAAA GGTCATACTG 1380
ACAGACGGTG CTGCCTGCCC CAGGACCCTG CAAGGCGTCT CCATCTGTCA GCTTCCCTGG 1440
TGCAGCCCCC TCCCTCTGGC CCAGAGACTC ACCCTCAGGC GTCCAAGGCT GAGCTGGACA 1500
AAGAGACCTG TGTGTACTTT GTAGGGGGCC TCAGCAGCCT CCACCCCCAT CTTAGGCTCC 1560
TCTGTCAGGA CCCCAACACA TGCCCCAGCT CCCACCAGAC TCGCCTTGGT ACTGTCATCC 1620
CACCACCTTC CCCCACAACA GCCTTTACAA AGGCAGTTTT CCCCTCCTCC CTGGAAAGCT 1680
TTCTGCCTCC CATGCTCATG TGTTTCCTGT TCTTGAATCT CCCTCCTCCA GGAAGCCACC 1740
AAGATAGCAA GTGAGCTGTG GAGTCAAACC GATCAGCTCC AACACTGCTG TGGGAGGTTA 1800
GCCAAGCGCT CATCCACTTC TGAACCTTGG ATTCCCACCA TCGACCCCCG ACCCTCCCCT 1860
CGCTAGGGCT TGTCATCGTC TTCTGCCCAT GGGGCAACCA AACCTCTCCA CGGAAGGGGA 1920
CAGGTCTCCT TGCTGCAGTG GGTAAAGGCC AGCGCAGTTA GGTGCAGGAG GCATTCACAC 1980
ACACGTGCAC ACTCCCCACC TTGCACACAT ATCTGCGTGA GCCGGGGAGA CCCTAGGGAA 2040
TGTGTGTGCA TGTTGTCTAT GCATGCGGGT AGAATCCGCA AACGGTGTGG AGACTCGGGC 2100
TCTTGGGTAC CTCTGAAGGC CCCTGAAGTC CCCATGGGCT TCTCCTTCCG TCCAGGGCAC 2160
CCTCTTATCA GGCCATGGCC CTGAGACGCG TAGTGCAGAC GCCCCCGGCG CTGAGGCTGA 2220
GGAGGCAGAT GGCCCCTCCC CGCACTGTGC AGGGCACCCG GTTGGGGGTG GAGGGGAGGG 2280
CCGCGTCGGT GAAGCGGGAA AGCCTAGTGG GAGGATTCCC TGGAGCTGAG GAGCCGGGGC 2340
CTGGGAAGGG GCGCAGAGGC TCCACCCAGG CGGGGGCGGG AAGGGCGGTG CCAGGGCGGA 2400
CAGCGGACGC GCGCGCCTGC ACGGACTCGG GCACACGCAG CCCTTCCGCG GCAGCGCCCG 2460
CCGCTCCACC GTCGCCATGG CTACCGGCTG GCCTGGAGCG GGGAGGGGCC CTTCCTCCCC 2520
TTCGGCGCCA ACAGGAGGCG ATTTGAGGGG ACTCAGCGTG ACTGGTGCAT CCCGGGGTTG 2580
GAAAATGGGT GGGTGCTTGC GACTGTCCAC GTGTGGGGGA CCCTGGGGTT CGCTTTGCGG 2640
TAGATGCAAA CGCCGCGGCG CGTGTGCGGG GCTCTGCAGT GGAGCCTGAG CCGTGCCGGC 2700
CGAGGCGTGG TGTGGGGGAG GCTGCCGGCC CTCTCGCGCG CGGGGTGTTC ACGCCTAGAG 2760
CGCTGGGGCT GGGGGCCTAC CACCCGGTCT CCTCCCAGCC 2800
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