| Tag | Content |
|---|
EnhancerAtlas ID | HS101-00909 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:27915710-27918640 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr1:27917248-27917259 | AATGAGTCAGA | - | 6.32 | | RREB1 | MA0073.1 | chr1:27916981-27917001 | CCACCCAGCACCACCCACCC | + | 6.09 | | TFAP4 | MA0691.1 | chr1:27917603-27917613 | ATCAGCTGTT | - | 6.02 | | Zfx | MA0146.2 | chr1:27916651-27916665 | CAGGCCCCGGCCGG | - | 7.01 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_00527 | chr1:27915162-27918007 | Adipose_Nuclei | | SE_00861 | chr1:27914193-27931151 | Adrenal_Gland | | SE_01588 | chr1:27912079-27922411 | Aorta | | SE_03939 | chr1:27916961-27918831 | Brain_Anterior_Caudate | | SE_05478 | chr1:27915165-27917912 | Brain_Cingulate_Gyrus | | SE_05814 | chr1:27913859-27923243 | Brain_Hippocampus_Middle | | SE_07770 | chr1:27913641-27918816 | Brain_Inferior_Temporal_Lobe | | SE_26518 | chr1:27909071-27932559 | Esophagus | | SE_27625 | chr1:27915801-27917333 | Fetal_Intestine | | SE_28547 | chr1:27916108-27917303 | Fetal_Intestine_Large | | SE_29557 | chr1:27915462-27922531 | Fetal_Muscle | | SE_31394 | chr1:27915365-27917462 | Gastric | | SE_31394 | chr1:27917763-27918706 | Gastric | | SE_33503 | chr1:27915499-27922187 | H2171 | | SE_40593 | chr1:27913008-27932820 | Left_Ventricle | | SE_42106 | chr1:27913545-27918982 | Lung | | SE_46630 | chr1:27914556-27917442 | Ovary | | SE_46630 | chr1:27917521-27918257 | Ovary | | SE_48058 | chr1:27914444-27919029 | Psoas_Muscle | | SE_51091 | chr1:27913567-27922874 | Skeletal_Muscle | | SE_54056 | chr1:27911548-27931728 | Spleen | | SE_54527 | chr1:27912777-27922283 | Stomach_Smooth_Muscle | | SE_62470 | chr1:27916580-27996594 | Tonsil | | SE_65253 | chr1:27915143-27922215 | Pancreatic_islets | | SE_68682 | chr1:27915388-27918381 | 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 |
| GH01I027588 | chr1 | 27914885 | 27923473 |
|
Enhancer Sequence | CCTAGGCAGG GAGGTCGAGG ACGAGGCCCA GATGTGCGTG TGCCTCTACA TCTGTCCACA 60
GTAAAACCTC TGGGCATTTC TTTGTCTTTG TCTGTGTCCG GGTGTGCACG CCTGTGCTCG 120
TGTGAGTACC ACTGGCTGTG TGTCTGTGCC TGTCTTTGTC TCTATATGTT TCTGGGCCTT 180
TGTCTCAGTG TGTGTGGCTG GTGATCTATG CCTGTCTGCA TGGCAGTGTC TGGTTTTGTG 240
GGTGTCTATG TGTGTCCTAG ACTCCATGCA TGTCTAAGTA CAGAGTGCCA GCATCCTGCT 300
GGACTACTGT TTGCATTTGT GGGTCCATGC GGCCTTGGTG TGAGTGAGGG CACATTGTGC 360
TTTTGAGACT GTGGGTCTAG GCTTCGGTGT ATCTAAGCGT GTGCTTGTGT TTCTGTATGG 420
GAGACTATGC CATGTGTTGT AGTATGGAGA TGCTTATCTA GGTCTGTGTG ATGTTTGTGA 480
GACCAAGGAT ATGTGTGTGT CTGTATCTGT GTGTTGGGTG TGAGGGGTTT GTCACAGACT 540
GGTGAGCAAG TTAATCTCAG ACTCTGTGAC ACGTGGAATA AAATCACGCT CCCATAATGG 600
GATCATTCGT CTTCCTGTCC AAGGAGAGAA CCAACCCTTC ACCCTCCGCC CTGGGGGAGC 660
CAGTGGGGCC AGGGCCAGGC ACCGGCCCCC ACCCAGGCCG CCTTCTGCCC TCAGCACCCC 720
CACCCCCTCC TCTGCTGCAC CAGGCTCATT CTGCCTCCAG AGTGCCCTAG TGCCCACTGT 780
GGGCTGGGCA GGGCTCCAGG ACATGTGACT GGGCCTTAGA GGCCTGTCCT GGGCCCCCTG 840
CCCCACCCAC TGCTGAGGAG AGCCCTGCCC TGAGATGAGA GCTGGGGGTA CAGGAAGGAC 900
TCTTCGGGCC CCTCCTTCTC CTGGAGGGGA GGGATGAGCT GCAGGCCCCG GCCGGGATTT 960
TCCATCTCTC AGCAACAAGA TTCCTGGTGA GCAGGCTGCG GGGTTTGGCA GCGCGCCTGC 1020
TGGAGACCCG CCCTCACCCG CCAGGATGCC TGGGTCCCTG GGGCCAGGCA GCAGCGAGTT 1080
CCCTGGGGAG CTGGGCGGGG AGGCCCACAA CTCCAACCTA CTGTTTGCCT GGGCCTGTGG 1140
GAAGGCCAGA CCCTTCCAGG CCCACACCTC CCAACCAAAG ATGGCTTCCC AGCACCCCCA 1200
GGCAAACTAT TACCCTTCCT CTGGCCTCCC CTAAGCCCCA GCCTTAGCTT AAGAAAGTAT 1260
TCCCAGGCCA GCCACCCAGC ACCACCCACC CCCACCACCC CTCAGCACAC ACCCAGCCTG 1320
GGTTCTGCAC CTCACCTCCA AGTCCGAGGG CTCTCAAGGT GAGTGTTTTG CTTCTCTCAG 1380
ACTTGGGGGG TCTGAGGACA AGGCTGTGTG TCCTGCATCT GTTAAATCCC TCTTGGTCTT 1440
AGCTCTCCTT CCTGGCTGGG CTGAGAGGCA TCAGGAGAGG ATTTAAGGTC CAAAGTTGGG 1500
GAAACTGAGG CAGTGAAGCC CTCCGCCCTA CTCATCACAA TGAGTCAGAG GCAAAATCCA 1560
GTCATCTGGA CTTGTCTTAA TGCTGCCTAG CAATAGTGGC TGCAGCTCTT TCTTTCTCGT 1620
GGGAGGGTGC AATTTCCGGA GGGGATGAGC ATCAGCTGGA GGGAGTGGGG AACAGGCAGG 1680
TGGGCTCCCT CAACCCCCAG CACCTTGGAT GAGCAGTTGG AGAGCAGGTT TGCTAAGAGA 1740
CTAAGGTTGA GGAGGAGAAA CGAGATGCTC CATGATTTAT GAGCCTAATT CTTTTCCCTT 1800
AAATTCCCCT CCAACCCCCA CCTCCCAGCC CCAGCCTGGT CCCTCCAGGG CCATGCTGTG 1860
GCCCCAGGCC AATGTCAAAG CCCTAACCCA TCCATCAGCT GTTGCCAGGG AGTTTCCACC 1920
CCAATGGGTT CCAAAGGGAG CGGCACAACT GACACTAGGG GCTCAGATTG ATGGGGAGGG 1980
AGCATGGCCC TAAGGAGTCT GCCAACAGAC CCCTGCACCC TCCTAGAAGC TGGGTGCTCA 2040
CAACATCCAG GGAGGAAACT AGGCTGGTGG GTGGGGCCCA GGAGGAGGTA GCCTCCCCGC 2100
TCTGGCACCA CACCCAGCCC TGCCCTTTCA AGAGGCCAGG AGACCTGGGA TCCCACGGGG 2160
CCCTGCAGCT CACAGGGTGT GTGACCTTGG GTGGTGACTG CTCCTCTCTG GGCCTCAGCC 2220
TTCCCACTGC ACAATGCAGA AAGTGGCTCA GATATCCCAG GTGACCACCT TTCGGCTCAC 2280
CCCCCTTAGC ATTAGGCCCT GCCCTCTGTC CAGAATCTGG CCCAGATGGG GTAAGGTCAC 2340
AGCAGCTACC TGGAGGAGTC CTCACAGCCA CCCAAGTCAG AGCTGAAGAG TTTATGGTGA 2400
TCACCCCTCC ACCACATGCC CATTTTCCAG TCCCTGAGAG AGGATCTGGA GTCTGCACCA 2460
AGACCTGAGT TTTACTGGTG GGGTGGTTAA GAGCACATGT TCTAGGGACA TACAGACCCG 2520
GATTAATGCC CTAGCTGCAC CAGTAACTTG TTATATGAAG TCCTGTGCCT TTTCTCAGCC 2580
TCAGATTCCC CATCTGTAAA ATGGGGTAAT AGTGCCTCTC TCCTAGGACT GTTGAGTTGA 2640
AATGAGAAAA TGCATGCAAA GGCCTTGGCA CAGTGCCTGA CACATAATAA GTGCTTGAAC 2700
AATGGTAGCG ATCATAATTG TGGTTAGTAT TAACATAAAT CCAGTGGCCA GGGAGAAGGG 2760
GGAAGAGGGA TCCCCGACCT GGCTGGAGGC GATCCAGCTT CATCCTTGAG CCAGGTCAGG 2820
ACCCCCAGGG TCTCAGCCCA GAAGGGCCAG CCGAATTCCT CGAAGCCCCC TAGCTGTCTC 2880
CCCTATTTGT TAAAGGCCTC TCATTAGTGA GCCTAGGCAC CTGCCCCTCC 2930
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