| Tag | Content |
|---|
EnhancerAtlas ID | HS180-15390 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr14:89894910-89897790 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr14:89896316-89896328 | TTCTGTTTACTT | - | 7.22 | | FOXP2 | MA0593.1 | chr14:89896317-89896328 | TCTGTTTACTT | - | 6.32 | | IRF1 | MA0050.2 | chr14:89896804-89896825 | GACTACTTTCGGTTTCCTGTT | + | 6.15 | | MEF2A | MA0052.3 | chr14:89896425-89896437 | TCTAAAAATAGC | + | 6.52 | | MEF2B | MA0660.1 | chr14:89896425-89896437 | TCTAAAAATAGC | + | 6.22 | | MEF2C | MA0497.1 | chr14:89896423-89896438 | GCTCTAAAAATAGCA | + | 6.29 | | Nr2f6(var.2) | MA0728.1 | chr14:89897773-89897788 | TGAACTCCTGACCTC | - | 6.22 | | ONECUT3 | MA0757.1 | chr14:89897008-89897022 | TTAATTGATTTTTT | - | 6.22 | | TP53 | MA0106.3 | chr14:89895326-89895344 | GGCATGCCTAGGCTTGTC | - | 6.71 | | TP53 | MA0106.3 | chr14:89895326-89895344 | GGCATGCCTAGGCTTGTC | + | 6.8 | | ZBTB33 | MA0527.1 | chr14:89896974-89896989 | AAGACATCGCGAGAG | - | 6 |
|
| | Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
| SE_02219 | chr14:89894547-89896375 | Aorta | | SE_02219 | chr14:89897002-89897996 | Aorta | | SE_09185 | chr14:89894205-89899234 | CD14 | | SE_25117 | chr14:89894930-89895317 | Colon_Crypt_3 | | SE_27314 | chr14:89894549-89896428 | Esophagus | | SE_27314 | chr14:89896960-89897446 | Esophagus | | SE_30170 | chr14:89893751-89897921 | Fetal_Muscle | | SE_32278 | chr14:89894688-89896213 | Gastric | | SE_32962 | chr14:89894422-89895631 | H1 | | SE_43326 | chr14:89894541-89896353 | Lung | | SE_43326 | chr14:89896920-89897880 | Lung | | SE_52261 | chr14:89893861-89897676 | Skeletal_Muscle_Myoblast | | SE_64066 | chr14:89893835-89897783 | HSMM |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 89895882 | 89896217 | | chr14 | 89897229 | 89897488 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I089425 | chr14 | 89891558 | 89899105 |
|
Enhancer Sequence | ACAACCAGGC GTCCTTTTTA AGTTGGCATT GCTTCCAGAG AGGAATCCTG AACATGTTTC 60
CTCTATGCCT CACACAGCGC CAGGCCAGCT GTCTAACAAT ATGGGTCCCG GAGGGGGTGC 120
TGCCCACGTT GGTGACGGCA GCCATGAGTG CCTGTTGCTC GCAGCAGACG TCAGAGAGAC 180
CTCAGCGCAG GGGTCCAAGC ACCTGGCCAA GGCACCCTGC GCAGGCCTCC ACGCCCCACG 240
AGTGCCTGCA GAGGCTACCT GAGGACCAAG GTGGGCATGC CACGGTGTCC TGGACTTCTG 300
GATGGAGGCC AGTCCCAGGG AGTGAATGGC AGAGCTCTCC GGAGGCTGCC CAGGCCAGGT 360
TCAATGGGAG GGATGAACTT CATGACATCC GTTCCAAAGA AATCCCACCT GCTACTGGCA 420
TGCCTAGGCT TGTCTTCCCC ACATACCAGC CTCCCAGGCA TGTCTCCAAG GGCTCAGTGA 480
GGAGGCAGCT GCAACAGTTC GCTTTCTCTT AATGATTTGG AGTTGGGAGG CACAGAGATG 540
GGGAAGAGGT AATGACCATT CCCAGTGATC CTGGACCTCC GTGTTGGCTG CGACCTTGAA 600
AAGTCATGCT GTCAACCCCT TTGTAGAAAA AATGCAGTTT TCTTTGTCCG TGGAAATCTG 660
GCCTCGCAGA TTTATTTGCT GTAGCAAGTT TCTTTACCCT CATCACACTG ATACTCAGAA 720
TTGAAACAGT TCAAACCTAC CCTGAAACAT CCTTCTCCCT CCAAATTCCA GTGACATCCT 780
CGGTCTAAAA CGCCTGGCAC CATGTGGGAG CCTGGCTCCG CTGCCTCTCA ACGCACTGGC 840
TTGCTTTTTG CTTTTGAGTA GCTTGAATAT CAAACCAAGC ACAAAGGGAA TCATACCCAG 900
GAGTTGCTGG AAAAAGCTCA TTTCATCCAC CTCATTCCCC CATTCTCTCT GGCAGACACA 960
ACTGATTTTT TTTTTTTTGA AGCCTGAAAA ACTTCTCATT TAAACTTGGG GTGCAAAAGG 1020
CATGTGAAGT GGGAGAGTTG CTGCCTGGAC CAGCGAAGGG TTAGCCAGGG AAGGATTCAA 1080
CGAAATACAA AAGCCAACAC AGACCTGAAG GGGAACAGGC GGCCCCAGCA ACAACTGCCA 1140
AACTGTCATT TTGCTCCGCG GCTGAACAGA AGGCTCGAGT AATGACAACC ACAAAACTCA 1200
TTTAAAGTCT GAAAAGGTGA CTAATGAGCT CATTCATGCT GGCTATAAAT TATTCACTAC 1260
AACACTGATC CCACTCAAGA CAAACAGTAA AGTAAACTTT AAACACAGAC ATCGCTGGCC 1320
TTCCAAAGTG GAACAAGTTA TGCCTGTAAA AGTTTTCACA ATGAGAGAGA TACTTGTCTC 1380
CCCCTTGTCT ATTGTCACAT TCGTTCTTCT GTTTACTTTT TTTTACTGCC TTTAATCAAG 1440
TTTAAGCAGA CACAGCTGTT ACACATTTAT TTCTCTGAGT TTTTTTCCAT TAGTTATTAC 1500
AAGCAATCAT GATGCTCTAA AAATAGCAGC AAATTATATT CTCTAGAAAT TGAAGGCTGA 1560
CCTTAAAATG AAGCCCAGGT CTTCAGAAAG AATATTCATA TGCACATGTT GGATAAATGA 1620
CAACAATGCA CAAAGGCAAA ATAAAAGTAC AAAGCTTTTT CCACTCTTTG AGAGGTTTTT 1680
GATTTGCTTC CAAATTTCCT TTGGTTCTGG TGGAAACAGG TTGCTTCAAA ACCTTACCAT 1740
ACAGAACCTG CTTCCAGTGG TCATGATTCC AGTTTGAAGG ATTTTCCTTC AAACTTACAA 1800
TCTTAAGGCA ATCAAAGAAG AAATGTTTCA TTTAGGCTTT TTCAGCACAG ATAAACACAG 1860
CAGCAGGTTG CTGAAAACCC ACCACATTGC TGCAGACTAC TTTCGGTTTC CTGTTTAATA 1920
TTAAATAAAG AATTTTAGCT CTTCTGTTTT TATAAACTGT GCTATTTGCT ACTACTGTCA 1980
CTACTAAAAG CATTATGACT GGGTGGATAA GTAGTCCTAT GATTTTCAAG CCTTCTTTTT 2040
TCTTTAATCT TAGTATCTAT TTTGAAGACA TCGCGAGAGT TAAGAGTCTC AAATCTGTTT 2100
AATTGATTTT TTTATTTTTA AAAGGCCCAA ATAAGTACTT CCGTTAGCTC TTAGATCTCT 2160
GAACATTATG TATTTTTAAA CCACTTTGAA TACTTTGAAA AGGGCCACAG AAAACACTCA 2220
TATTCAAATA CCACCAGACG GAGGTTCTGC CTAACCAAAA GTAAAAGCAG AAAAGTTTAA 2280
AGCTGAATTG TGCCCTGCAC ACACCTTGAG ATTGTAGGGG TGAAATGAAT GGTCTTGGGC 2340
CGGGGATCTT GCTAAAGGCA TGATAAATCA TGCGTTGCAG GCAAATTAAG ACCCAGGCTC 2400
TAACTTGAAC CTCAGACTGT GCCAAACTCC ATCTCCATTT AAGGAAAATG GTTTTCTCAG 2460
TTTCTTGCAC ATGACCTAAA GGCTTGTCCA GTCATTTCCG TTGTCTGAAA TGCAAAGCAA 2520
TCTTTCTTTT TTAAGTAGAG AAAGAAGAGT CCTGAAATAT TTATAGGAAA GTGCTTCACT 2580
ACCTACTGAC AGCAATGTGG TTGGTCTCTA CGTGTTTAGC ACATTTTTTT TTGTTTGCTT 2640
GTTTCTTTGA GACAGAGTCT CTCTCTCTCT CCCAGGCTGG ATGGAGTGCA GTGTTGTGAT 2700
TTCAGCTCAC TGCAACTTCT TCAGCTTCAC TTGAACCGGG TTCAAGTGAT TCTCCTGCCT 2760
TAGCCTCCCA AGTAACTGGG ATGACAGGCG CCCACCACCA CACCCGGCTA ATTTTTGTAT 2820
TTTTGGTAGA GACAGGGTTT CACCATGTTG GCCAGGCCGG TCTTGAACTC CTGACCTCAG 2880
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