| Tag | Content |
|---|
EnhancerAtlas ID | HS180-01475 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:44022320-44025600 |
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 | | RREB1 | MA0073.1 | chr1:44022452-44022472 | TGGTGGTGGTTGCTGTGGGG | - | 6.93 |
|
| | 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 | CTTCTCGTGT GTCTTTGGGT TAGTAACTAT GCCTCTGACC CTCATTTGCT CCATCTGTAA 60
ATGGATATAA TGCCTACCAC CCAAGCTGGT TTGGAAGATT GAATGCTGTG TATGAAGCGC 120
TTCCCAGGAG TGTGGTGGTG GTTGCTGTGG GGCTGGAAGC TGTACATCTT GAGGCCTCAC 180
CACGTGAGCT GAAGGTGGTT GGCCTCCGTG CTGCGTGGCA TCATCCGGGT GATGCAGCTC 240
CACTGCCTGC TCCCACGGGG GGACATACCT GTGCAATAGG AACTCAGAGA ACAGGCCCTG 300
GGCCAGCATC ACTGATTGCT GAGTGTTCTC AGGCTCCTCC CTGCCACTTC TGACCTGTTT 360
CCCCACTCGT GACCTGGGGG CAAGTATTTC AATGCTGCCC AGTCCTCCTA TTGGCAGCTG 420
TCCTAGCAGG GAGCCATCTG CCCTGCCCTG GCATTTGGGA GGTGGCTGAA GGACCAGAGG 480
CCCCAGAGGG CTTCTTTTCA GGCTCTCAGA TTGGGGAACA GGGCCTCCTT GTTAGTATTG 540
AAAGAGGAGT CCTTCAAAAG CGCCTAAGCC CCAGGTCCTG GGTCAGGAGC CCTCTTACCT 600
CTGCCACTGC CCTGGGCAGC CTTACCTTTC AAAGGGTTGA GGAGGATGGA GGTGGTCTTT 660
CAGGCCTGGG GTGAGGAGGA CGGACTTCAG ACTGACAGGA GGGGCTGGGT GTGGTGGCTC 720
ACGCCTGTAA TCCCAGCACT TTGGGAGGCA GAGGCCTGCA CATCACTTGA GGTCAGGAGT 780
TCGAGACCAG CCTGGCCAAC ATGGCAAAAC CCCATCTCTA CCAAAAAATA CAAAATTAAC 840
TGGGCGTGGT GGCGCACGCC TGTAGTCCCA GCTACTTGGG AGGCTGAGGC AGGAGAATTG 900
CTTGAACCCA GGAGGAGGAG GTTGCAGTGA GCTGAGATTG CGCCACTGCA CTCCAGCCTG 960
GGCGACAGGA GACTCCATCT CAAAAAAAAA AAAAAAAAAG AGGACCTGCA GGAGGTGCCT 1020
CCGTTTGGTT TCTCTACCAG GGGCCAGCAG TATATGTTTG CGCTTCTGGG GTGTGAGAAG 1080
TGTCTGATGA GGCTGGGGAG AGTGTGGCGC AAGTACCCAG ACCCTGTCCA TGCTCCGGGG 1140
AAGGGTGTGG AGCTGTGGGC CTGAGTGAGC CCCTCCTGCT TCTGAAACAT AGCACCAGGA 1200
AGACAAAATG CTGACTTATC CTGCTGGTCT GTATAACCTT GGCCAGCATT GGGCTTGACA 1260
GAAAGGCGTG CCGCAGGAGG GCCAGAGGGA AGCAGCCCAG AGGGTGAACA CCCGCCCCCT 1320
GCCCCGCCTC ACCCCACCCC TCCCCTCCCT CCTAGGAGGA TCAAGAAAGC TGGGTGCCTG 1380
CAGGAACTGG GTGAAAGGAT GGTTGGACTT GGACTGGAGC TCTGGGGTGG GGCCGGCAGG 1440
AGCCAGGGCC ATTCTTGGGA GGCCACCACA GGGTACGAGG AGGGCTGGGG AGGGGATGGA 1500
GCTAGTTGGG GTCGGGGAAG TAAGAGTCCT TCCTGAGTTG CACACAGCTC TCCCTGTGAG 1560
CTGGTCTCCT TGGAGAATGG CTGAGGGCTG TCTGGGGTGA ACTGGCTCAG GTGAAGATCA 1620
GTGTGCCCCC AAAAAGGAGT CCAGGCCTGC AGTCTGTTCT GTGCCCTCTG CCTTTGCCTC 1680
ATGTCACACC AGGCCCAACT GCTGTGGCTC CAGGGCCACT CCCACCACAG CCCGTGGGAG 1740
TGCCCCCCCA AATCCCCCAC AGCCGTGCCC TTTGCACCTC GCATCTGAGC AGGATTGTTA 1800
TTCCCAGTGT GGCCTCCCCT TGACACCCCC GCCAGGACTG CATACGAGGT GGGGGTGCCC 1860
AGCACAAGCT GGCCGGGGTG AGCCTGTCCT GGCTGTGATG AGCGTGGGGC CCGCCGCCCA 1920
GCGTTCCTGT CTGAGTGGTA ATTGAAGCCA TTAGCGCGCC AGCCTCTCCC TCGCCGGGTA 1980
ATGGCAGGAA AAGCTCTTCT CGCTCCGCAC TCTTGAGGCG GCGGCTGAAT CACTCCCCCT 2040
CCAACCCGCC CGCTGCCGCC ACTGAGACAG GGAATCTGAC ATTTTCCCTC ACCAGGGAGG 2100
GGGAGCCCTG GGGGAGGGGA GGGAGGCAGG CCTGGATTCC TGGCCTTTCC CTCCAGGAGG 2160
TTGAGGGGCA GTGAAGGTCT TGGAGCTCAG TCTGTAAGTC ATGGATTCAC CTGGGGCCGC 2220
AGATTTCAGG CCTGGAAGGA CTGGCCGGGA AAGCCCAGGA GGCCGCCAGA CATTCAGTGG 2280
TGTGGGGAGG GCACTGATGA CTTTGGGTAG GTTCTGGGAG GGACAAGGAG GCGGGGAGAA 2340
GAAAGAAGCT GTGGAGCAGA GATGAGCTGT TTTGGACTTC TCCTGGGGGG CTTAGCTCCA 2400
AGGGTTCTGA GTACAGGTAG CATTACTTGT CTTGGGGTCA TTGATAGGGC AGATAACGTG 2460
CACTGTTCGT GTGGTGTGGG TGCCCTGTGT GCCATGTTTA AGGCAGTGTT TGTGTGAAGT 2520
GTGTGGTGCA GTGTGTGCAG CAGGGGTGCT GCCTTGCAAG CTGTGCGCAC AGAACGGGGT 2580
GTGCAGCGGT CAGCGCACAC GTTACCATCA GGCAGTGGGG AAGGGGCAGT GTGTGCAGGA 2640
GGCACTGCAT GCTGTATGGG CTGTGTATGC AGCGCGCAGT GTTTGTGTGC ACGTGTGTGC 2700
GTCAGGCAGT GCGTGGTGTG GTGGTAAGCA GGTAGTGAGT ACCTTATGGG CTATGTATAC 2760
AGCAAGGCAT ATGCATCAGG CAGTGTGTGG GCAGTAGGCA GTGTGTGTGT GTGTTATCAG 2820
GCAGTATATG TGTGCGGTGT GCCGTGCGGC AGGCTACCTG TGTTTATATC GGGTAGTGTG 2880
TGTGTGTTTA TGTGCAGCAA GGGTGTGCAG TAGGTGTGCA GTAGACTGTG TGCAGCAGGC 2940
GTGTGTGTGT GTACAGCAGG TGGTGTGCAG CAGGCAGTGT GTGTATGTAT CAGGCGGGGT 3000
GTGGTGTGTG TTTATGTGCA GCATGCGGCG AGTACTTTGT GTGGTGTACA GCAGGTGGTG 3060
TGCGGCAGGC TGTGTGTATG TATCAGGCTC TGTGTGTGTG TGTGTGTGTT TGTACAGCAG 3120
GTGGTGTGCA GCAGGCAGTG TGTTTATCAG GCAGTGTGTG GTGTGTGTGT GCATCTTTAT 3180
GTGCAGCGAG TAGTTTGTGG GGTGTGCAGC AGGTGGTGTG TAGCAGGCTA TGTATGTATC 3240
AGGCTGTGTG TGTGTGTGCG CGCGTGTGTA CAGCAGGTGG 3280
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