| Tag | Content |
|---|
EnhancerAtlas ID | HS059-02712 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:151474560-151475900 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RORA | MA0071.1 | chr1:151474901-151474911 | TGACCTTGAT | - | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_23540 | chr1:151475048-151475747 | Colon_Crypt_1 | | SE_27750 | chr1:151473711-151476226 | Fetal_Intestine | | SE_28641 | chr1:151473812-151476533 | Fetal_Intestine_Large | | SE_53040 | chr1:151474354-151475795 | Small_Intestine |
|
| | 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 |
| GH01I151501 | chr1 | 151473799 | 151476189 |
|
Enhancer Sequence | ATCCCCTTGA TTAAGCACTG TCAAAATCCA ATCCCATGGG TACTTCCCTA CTCTTACCAC 60
TAAACGTTGG CCAGTTCTTG CAGGATACTT TGGGTTATAG TCCCTTTCTT TCCTTATTAG 120
GCCTAGTATG TCCTTAGCTA CCAGACTATG CTGTAATTTA ACCCATGAGA GTTTAAGATT 180
AAGATCTTCA CAGTCAGGAG ATCATGGGAG GGGAGAGGCC TCTGCAGTGT CTTAAGGCTC 240
TGAGGGTTCA GAGGAGTGCA GAAAGCCAGA ATCTTTGGGG GGACCTGCCC AGATATTTCT 300
ATTCCACGTA TTAGGGTCCC AGGTTTTCCC AAGCAGAGTC CTGACCTTGA TTGCAGATCT 360
GCCTCTGGGA GCTCTATTGA AGTCCTCGAG TTTGGTCTTC AGATTTTTTT GCTCTCTCAC 420
TGCTATAGAT AAGGGCCTCT TTGTAAGCCA TCAGAAAGGC CCTCTGACCT TCACAGTTAA 480
TTTCCAACGT TTGTTAACTA CTCTCAGCTT TTCATTTTCT CCTGGCAGGG CCCAGTGCAA 540
CTTAATAACA GCCAGCCAAT TCCATTGTCC CTATACTCAC TGCTGTCCCT CCGCCTACCC 600
CCTATGCCTG AACTGTTCCA CCACAGGAGC ATTCTCTCAT TTCACATCAG TGAAAATTTA 660
GCAACTTGGC TACCATCTTG TTCCAGAGAC TACCTGTACC CCACAACATC CAGGAGGGGT 720
TCTTGTTGCC AGCCAGGCAG TGAGTACTGC AGTTCCCTAA ACCTATCTTA CTGCTCGCTT 780
TTTCAGACCA CTTCTGGAGT GGTCACCTGA GTCAGTTCAG GTGGTCTGGG GAGCAGATAC 840
TGAGACAAAG TTAGGAGTGC AAGAGGCTTA CTGGCTGGCA ACACCTGTGA AAGATAAAGA 900
AGGAGGCAGG AATGGGCAGA GAAAGACTTT GGATAGGCTT CCCTATCCTG ATAAAGTAAA 960
GGAAGGCAGA AGCAAAATCG GGCAAGAAAA ACCTCAAGCT GTGGTGCAGA TCCTTCCAAG 1020
TGGCAGTCTA CCCAGTGGAA AGCACCAGGG CAAAGGTTAT CACATAGAGA AATCAACAGT 1080
GGGCAGAAAC GGCCAGGTCC CAGTAACCAC ACTGTCAGTC ATTGGCTTGG GGCTGTTCAG 1140
GAAGAGTGTG GCCTTAGCTC TGACATGGTA GTGGATCCCA AAGGTGATGC AGCTGTGGGC 1200
TGACAGTGAA TTGCTTTCTG GCAGTTGAAT GGCAGATTCT TTCTAAGGGA TGTCATGGCT 1260
GCCACATCAG GTATTTTTGT CTTGGAGTTC AGTGCTATTT CCATATGTCA TTTTGCCTCT 1320
GTATTATGAG ACTTATACTT 1340
|
