| Tag | Content |
|---|
EnhancerAtlas ID | HS101-01355 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:43749040-43751110 |
Target genes | | Number: 27 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf12 | MA0742.1 | chr1:43750480-43750495 | GGCCACGCCCTCCTC | + | 6.74 | | SP4 | MA0685.1 | chr1:43750478-43750495 | CTGGCCACGCCCTCCTC | + | 6.06 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_29457 | chr1:43748843-43752786 | Fetal_Intestine_Large | | SE_31961 | chr1:43749328-43752683 | Gastric |
|
| | 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 |
| GH01I043281 | chr1 | 43747379 | 43749176 |
|
Enhancer Sequence | TAGAAAATAA CATAGGTATG GGTGTCAGGG ATGGTCACAG GGTGCACTTT CCAGGTCACA 60
CTCACAGCCA TGGTAGCCCT GCACAAACTC TGGGGACTGG ACAACTGACC ACACCAGCTC 120
TCCACAGAAG AGAAACAAGC TGAGCCTACA GAAACTGGCT ATTTGTAAGG GACCATCACA 180
GGGTTTGGCT CTGGAAGCTG CTAAAAAAAA AATAAATTGT AGAACTTACT GAGCATTCCT 240
TATAATTCAA GCACCAGGCA TCATGCTCAC AAAACCCAGT AAGGTAAGTA TAAACATTAT 300
CCCCACTTTA TAGATGAGGG CTCTGAGGCT GAAAAAGGTG AACTGACTCA ACTAAAGTCT 360
TCAGATTCGA ACCCAGAGCC CAGTCTGTTG CACTGCTTGG TAAGCTGAGG ATGGGAGACA 420
GGGGCAGAGG TGGGTCCTGG CTCCCGAAGG TCAGAAAACA GCAATTGCTT GGAGCTACCC 480
AGCCAAAGCG GAGACCACAT ATGGGGAGGG TGATGCAAGT TGCTACTGAG GACAGGGGCC 540
CTGGACACAG CCAGAGCAGC CCTGGCCCTT CTAAGTTGAA AGCCGCTGCT GCCCACCTCT 600
ACCCTCAGCC CTTCAAGCAA ACCCCTGTCC TTTCACCTCT ACTCAAAGGA GGCCCACACT 660
CTGCCCCCAC AGGGAGGCTC AAGCCAGGGA GTATCCAAAT GAGGATCACC TGAATCAGGA 720
AATTATCACC CAGGGCTGGG GACACCTAGA GGAGGAACAC TTCAATTAGG GGAGTAGCTG 780
GAGGAAGATC ATCCAGGCAT GGAAACACCT GTAGGAGGAG CACCTGGATC AAAGGAGTGT 840
CTGGAGGAGG CGCACCTGAA TCTGGGGAGT ATCTAGAGGA GGAGCATGAA AGTTAGAAGT 900
ACCTGGCAGA CGAACAGCTA GGGCAGGAGC ATATCTGCCA GTGGAGCACC TGAACCAGGG 960
GAGTCCTTGG GGGCAGAGTA GCCGGGCTAG GGAAGTACTT AGGAGAGAAG TTGAGGGGAG 1020
TACCCCAGTA TATTCTTTGA TACAAGTGCC TTCAAACCCC CCCCAACCTC CTCACATCCA 1080
ACCTGGTATC AATCCCCATC ATGTCTTCCA CTAAACATCT CTGGAATGAC AATACCCTCT 1140
TCTCCACCCC ACTGCCACAG CTGAGTCCAA GCCACCTTCC TCTTGTACTC TAGCCATAAT 1200
CTCCTAACTG GGCTCCCCAC CTCTGGTCTC TTCCACAGAG TGATGGGCCT ACAACCCAAA 1260
TCTGACCCCA TCACTAGCCT GGTTAAAATC CCTTCAAAAG CTCCCCATGC CCCACAGTGC 1320
CTTGCAATCC AGCACACGGC CCTCAAGCCA AACTCTTCTT CCTCTTCTCC ACAGTTCCCT 1380
CCCCAGCACT TCAGACAGAC ACACATGCCC TCCTCCCACT CACCCACCCT CCTGCTCCCT 1440
GGCCACGCCC TCCTCAGTTT TTGGGGCGCC AGTCTGTCAA GGCCAAATCA GACCATACCT 1500
GCCTGTGAGG TTGTCCCTGG ACCTACCCTG GATGACCTGT CACCATCCTG CCCAGTCAAC 1560
CACCAGTCAG AACCAGTCAT TGCTAGGCGG GCAGCTCCCC GTGGGCAACG GCTGGCTGAA 1620
GGATCTGTAC CCTGGCGCTG CAGGGAGCTG GGCGTTCAGC CCCTCAGTGT GGTGCTTGTG 1680
AAATTAACGA GGGGAGCGTG AGAGTGAATA TACAGGTGGG AGCGGGAGAG ACGTCCTGGG 1740
AAGGAGAGGT CAGCTGCTCA TTCATTCCTC AGCCTGCTGT GGGCCTCATC CTAGTACTAG 1800
GTCCGCAAAA CATGAGAATG TGTTACACTG GAATGAACTG AATTCAATTT GACGTTTCTA 1860
AGGTTGTATT CCTATTCCTT TCCTCCCTGC CCTGTGAATT CTTCCCAAGA AGACACACAC 1920
ACACTAACCT TCCAAGGGTG CATATACACT CCCCAACAGG CCTCTGAACT CACAGCCCAC 1980
ACTGATCTGC CCATCCCCCA TACGCACAGC CCCTCCCCCC AGGTCACACT TTCCTCCACC 2040
AACAAACACC CCTCTGACAT GCACAGACAC 2070
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