| Tag | Content |
|---|
EnhancerAtlas ID | HS030-00838 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr1:44022820-44025600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:44024432-44024450 | GGAGGGGAGGGAGGCAGG | + | 6.34 | | Mafb | MA0117.2 | chr1:44023524-44023536 | AAAATGCTGACT | + | 7.22 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_00616 | chr1:44009256-44025211 | Adipose_Nuclei | | SE_04240 | chr1:44023611-44026224 | Brain_Anterior_Caudate | | SE_05040 | chr1:44023306-44027093 | Brain_Cingulate_Gyrus | | SE_05962 | chr1:44023210-44026924 | Brain_Hippocampus_Middle | | SE_07193 | chr1:44023786-44025089 | Brain_Hippocampus_Middle_150 | | SE_08033 | chr1:44023627-44026877 | Brain_Inferior_Temporal_Lobe | | SE_23218 | chr1:44022089-44026653 | Colon_Crypt_1 | | SE_23829 | chr1:44022157-44023119 | Colon_Crypt_2 | | SE_23829 | chr1:44023263-44026674 | Colon_Crypt_2 | | SE_24870 | chr1:44022071-44023154 | Colon_Crypt_3 | | SE_24870 | chr1:44023259-44025244 | Colon_Crypt_3 | | SE_26649 | chr1:44022053-44025193 | Esophagus | | SE_27645 | chr1:44022136-44025907 | Fetal_Intestine | | SE_28595 | chr1:44022065-44026100 | Fetal_Intestine_Large | | SE_31538 | chr1:44022050-44025040 | Gastric | | SE_33537 | chr1:44023245-44025799 | H2171 | | SE_41575 | chr1:44022120-44023117 | LNCaP | | SE_41575 | chr1:44024391-44026778 | LNCaP | | SE_50363 | chr1:44021974-44023142 | Sigmoid_Colon | | SE_50363 | chr1:44023204-44026309 | Sigmoid_Colon | | SE_52524 | chr1:44022166-44025322 | Small_Intestine | | SE_56987 | chr1:44022407-44023150 | VACO_400 | | SE_56987 | chr1:44023247-44023613 | VACO_400 | | SE_56987 | chr1:44023728-44024680 | VACO_400 | | SE_65452 | chr1:44022315-44025132 | Pancreatic_islets | | SE_69138 | chr1:44023472-44026821 | 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 |
| GH01I043556 | chr1 | 44022192 | 44025767 |
|
Enhancer Sequence | GGCTCTCAGA TTGGGGAACA GGGCCTCCTT GTTAGTATTG AAAGAGGAGT CCTTCAAAAG 60
CGCCTAAGCC CCAGGTCCTG GGTCAGGAGC CCTCTTACCT CTGCCACTGC CCTGGGCAGC 120
CTTACCTTTC AAAGGGTTGA GGAGGATGGA GGTGGTCTTT CAGGCCTGGG GTGAGGAGGA 180
CGGACTTCAG ACTGACAGGA GGGGCTGGGT GTGGTGGCTC ACGCCTGTAA TCCCAGCACT 240
TTGGGAGGCA GAGGCCTGCA CATCACTTGA GGTCAGGAGT TCGAGACCAG CCTGGCCAAC 300
ATGGCAAAAC CCCATCTCTA CCAAAAAATA CAAAATTAAC TGGGCGTGGT GGCGCACGCC 360
TGTAGTCCCA GCTACTTGGG AGGCTGAGGC AGGAGAATTG CTTGAACCCA GGAGGAGGAG 420
GTTGCAGTGA GCTGAGATTG CGCCACTGCA CTCCAGCCTG GGCGACAGGA GACTCCATCT 480
CAAAAAAAAA AAAAAAAAAG AGGACCTGCA GGAGGTGCCT CCGTTTGGTT TCTCTACCAG 540
GGGCCAGCAG TATATGTTTG CGCTTCTGGG GTGTGAGAAG TGTCTGATGA GGCTGGGGAG 600
AGTGTGGCGC AAGTACCCAG ACCCTGTCCA TGCTCCGGGG AAGGGTGTGG AGCTGTGGGC 660
CTGAGTGAGC CCCTCCTGCT TCTGAAACAT AGCACCAGGA AGACAAAATG CTGACTTATC 720
CTGCTGGTCT GTATAACCTT GGCCAGCATT GGGCTTGACA GAAAGGCGTG CCGCAGGAGG 780
GCCAGAGGGA AGCAGCCCAG AGGGTGAACA CCCGCCCCCT GCCCCGCCTC ACCCCACCCC 840
TCCCCTCCCT CCTAGGAGGA TCAAGAAAGC TGGGTGCCTG CAGGAACTGG GTGAAAGGAT 900
GGTTGGACTT GGACTGGAGC TCTGGGGTGG GGCCGGCAGG AGCCAGGGCC ATTCTTGGGA 960
GGCCACCACA GGGTACGAGG AGGGCTGGGG AGGGGATGGA GCTAGTTGGG GTCGGGGAAG 1020
TAAGAGTCCT TCCTGAGTTG CACACAGCTC TCCCTGTGAG CTGGTCTCCT TGGAGAATGG 1080
CTGAGGGCTG TCTGGGGTGA ACTGGCTCAG GTGAAGATCA GTGTGCCCCC AAAAAGGAGT 1140
CCAGGCCTGC AGTCTGTTCT GTGCCCTCTG CCTTTGCCTC ATGTCACACC AGGCCCAACT 1200
GCTGTGGCTC CAGGGCCACT CCCACCACAG CCCGTGGGAG TGCCCCCCCA AATCCCCCAC 1260
AGCCGTGCCC TTTGCACCTC GCATCTGAGC AGGATTGTTA TTCCCAGTGT GGCCTCCCCT 1320
TGACACCCCC GCCAGGACTG CATACGAGGT GGGGGTGCCC AGCACAAGCT GGCCGGGGTG 1380
AGCCTGTCCT GGCTGTGATG AGCGTGGGGC CCGCCGCCCA GCGTTCCTGT CTGAGTGGTA 1440
ATTGAAGCCA TTAGCGCGCC AGCCTCTCCC TCGCCGGGTA ATGGCAGGAA AAGCTCTTCT 1500
CGCTCCGCAC TCTTGAGGCG GCGGCTGAAT CACTCCCCCT CCAACCCGCC CGCTGCCGCC 1560
ACTGAGACAG GGAATCTGAC ATTTTCCCTC ACCAGGGAGG GGGAGCCCTG GGGGAGGGGA 1620
GGGAGGCAGG CCTGGATTCC TGGCCTTTCC CTCCAGGAGG TTGAGGGGCA GTGAAGGTCT 1680
TGGAGCTCAG TCTGTAAGTC ATGGATTCAC CTGGGGCCGC AGATTTCAGG CCTGGAAGGA 1740
CTGGCCGGGA AAGCCCAGGA GGCCGCCAGA CATTCAGTGG TGTGGGGAGG GCACTGATGA 1800
CTTTGGGTAG GTTCTGGGAG GGACAAGGAG GCGGGGAGAA GAAAGAAGCT GTGGAGCAGA 1860
GATGAGCTGT TTTGGACTTC TCCTGGGGGG CTTAGCTCCA AGGGTTCTGA GTACAGGTAG 1920
CATTACTTGT CTTGGGGTCA TTGATAGGGC AGATAACGTG CACTGTTCGT GTGGTGTGGG 1980
TGCCCTGTGT GCCATGTTTA AGGCAGTGTT TGTGTGAAGT GTGTGGTGCA GTGTGTGCAG 2040
CAGGGGTGCT GCCTTGCAAG CTGTGCGCAC AGAACGGGGT GTGCAGCGGT CAGCGCACAC 2100
GTTACCATCA GGCAGTGGGG AAGGGGCAGT GTGTGCAGGA GGCACTGCAT GCTGTATGGG 2160
CTGTGTATGC AGCGCGCAGT GTTTGTGTGC ACGTGTGTGC GTCAGGCAGT GCGTGGTGTG 2220
GTGGTAAGCA GGTAGTGAGT ACCTTATGGG CTATGTATAC AGCAAGGCAT ATGCATCAGG 2280
CAGTGTGTGG GCAGTAGGCA GTGTGTGTGT GTGTTATCAG GCAGTATATG TGTGCGGTGT 2340
GCCGTGCGGC AGGCTACCTG TGTTTATATC GGGTAGTGTG TGTGTGTTTA TGTGCAGCAA 2400
GGGTGTGCAG TAGGTGTGCA GTAGACTGTG TGCAGCAGGC GTGTGTGTGT GTACAGCAGG 2460
TGGTGTGCAG CAGGCAGTGT GTGTATGTAT CAGGCGGGGT GTGGTGTGTG TTTATGTGCA 2520
GCATGCGGCG AGTACTTTGT GTGGTGTACA GCAGGTGGTG TGCGGCAGGC TGTGTGTATG 2580
TATCAGGCTC TGTGTGTGTG TGTGTGTGTT TGTACAGCAG GTGGTGTGCA GCAGGCAGTG 2640
TGTTTATCAG GCAGTGTGTG GTGTGTGTGT GCATCTTTAT GTGCAGCGAG TAGTTTGTGG 2700
GGTGTGCAGC AGGTGGTGTG TAGCAGGCTA TGTATGTATC AGGCTGTGTG TGTGTGTGCG 2760
CGCGTGTGTA CAGCAGGTGG 2780
|
