| Tag | Content |
|---|
EnhancerAtlas ID | HS078-00851 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr1:44732850-44734050 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr1:44733113-44733124 | AAGCCATAAAA | + | 6.62 | | ZNF263 | MA0528.1 | chr1:44733066-44733087 | TCCCCTCCTTCTTCTTCCCTC | - | 6.46 | | ZNF263 | MA0528.1 | chr1:44733063-44733084 | TCCTCCCCTCCTTCTTCTTCC | - | 6.53 | | ZNF263 | MA0528.1 | chr1:44733059-44733080 | CCTCTCCTCCCCTCCTTCTTC | - | 6.5 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_23389 | chr1:44731722-44733138 | Colon_Crypt_1 | | SE_23389 | chr1:44733254-44737294 | Colon_Crypt_1 | | SE_24224 | chr1:44732365-44733121 | Colon_Crypt_2 | | SE_24224 | chr1:44733284-44733803 | Colon_Crypt_2 | | SE_50790 | chr1:44731489-44735398 | Sigmoid_Colon |
|
| | 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 |
| GH01I044266 | chr1 | 44731749 | 44735355 |
|
Enhancer Sequence | GCAGGGAGAA GCTAGCATAC TTAGGTAAGG TGGAAACATA AGCTACAAGA CTTGTAGGTG 60
GATGAAGAGG GGAAGATCTG GGGCTTATTT CCTAAGCAGT TTGTCCTGAC CCTGGAGATC 120
TGCCATTTCC ATATCATCCT TCTGGTTAGG AGAGCCCTCC TGACCACAGT AGAAAGGGGC 180
TCATTCTCCC AACCCCCAAT TCCTATGGGC CTCTCCTCCC CTCCTTCTTC TTCCCTCCCT 240
TTCTTTCCTG CAGAGCTTCC CTCAAGCCAT AAAAATAAAA TAAAACACAA ACACCCACAG 300
TCCAGGAGGA GGGCGTTGGA CAGATAATGG GCATTTTATA TCTTTTTATG ACACTCCCCA 360
TAGGCAGCTC AGCAATCACA GCGCAATAAA GGCAGGCATG CAGCTTGCAT AGTTAAACAA 420
CTGCCGGGTA ATTAGGCACA GCAAACACAC CACTGGGGAG GCCTCAGGCT TGCCCTGGGA 480
TCTGCCTGCA GCCCGCCTGC CTGCTTGCAG CCAAGTAGGT GCCAAGCCCA GGCCTAGCAA 540
CATAAGACCT GGTTGTGGTG CTGGGGACAG GCCACTGACA GCTGCCATAA ACACGCTTGG 600
GTTCATGCCT GTGCAAACTC AAGCCTACCT GCCCACACCC ACACAAAAAC ACTCCCTAAG 660
CCAGCCTGGA CCTTATCTCC CCAGGAGGGC CACCCTCTTT TCCAAGTAGG GCAATCTAGG 720
GTATCTTGAG GGCCCCGCTT TAGGGCCTTT GAAGAAGTCA CAGCAGGCAC TAGCAGGGAC 780
TAGCTCATCG GGGTAGCTCA AAGCTTATCG AGTGGCACAG GCAGGAGGCA CAGGAACATA 840
CAGACGTGTT TACATGGATC CTCTGTCTCT TGTAAATTTT TACTCAGTAC AGAGCTGAAT 900
TCAAAATAAT TTTTAACACA GATGATTCAT ACACACCCTA TATACATATT TCTATCACTG 960
TACTTACCAC TTCTATTGTG TTTTTCCCCC ATCTGCCTAT TGACCCATCC ATCTTCCCTA 1020
CCAGACCAGG AGCTCTGTAC AGGTGGAGAT CAGGTCTGAG TCACCTCTGA GTCCAGAGGT 1080
CCCAACCCAT AGGGTGACTG GTGGCTGGAG GTGAATATAG ATGTCCCAGC CCAGGCAGAG 1140
CACAGGACTC TTGCTACCTG AGACCTAGGT CCAGGGGATG TTAGCCCGAA CAAGAGAGAA 1200
|
