| Tag | Content |
|---|
EnhancerAtlas ID | HS047-07485 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr12:12185450-12186680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:12186449-12186468 | TAGCGCCACCTGGTGACCA | - | 7.45 | | Crx | MA0467.1 | chr12:12185747-12185758 | TTAATCCTCTT | - | 6.14 | | HNF4G | MA0484.1 | chr12:12185642-12185657 | TGGCCTTTGGCCTGG | - | 6.03 | | INSM1 | MA0155.1 | chr12:12185901-12185913 | TGCCTGGGGGCG | + | 6.14 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_19498 | chr12:12184887-12186728 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_39774 | chr12:12184589-12186557 | Jurkat | | SE_49985 | chr12:12184383-12189228 | RPMI-8402 | | SE_66709 | chr12:12184589-12186557 | Jurkat |
|
| | 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 |
| GH12I012032 | chr12 | 12185000 | 12187030 |
|
Enhancer Sequence | ACTGAGCCAT GCTAAGGTTG GTGAGCCGCT GCTCTGGAAC ATTGATCCCT CCCAAACTGC 60
AGCAAAGCAA GCACCTGGGT GTAGCTCTGG CTGTGTAGGT GCTACTACAA TCTGCTGGAG 120
TCACTGCTTG TCGGCAGAGA TGCCGTGGGA GCTGGCCTGG GTGCCTCCAC GTTGGCCGTC 180
ACCACCAGGC AGTGGCCTTT GGCCTGGAAT CGAAGGTACC AGAGGGCTGA TAGCTCAGTT 240
TTTTTATGGC ACCAAGAAAA GACTTTCAGA TTGGAGGTAT GGGATTTTCT TTATTTTTTA 300
ATCCTCTTTT AATATAAAGT GGCCCCTTAG CAAACTTTCA AGATATTTCA CATCAGAACT 360
GGCCGGGAAA TCCGGCATGT GGACAGACAC GGATATGCCG TGTGCATTTT TCCGTTGGAG 420
GAAGAGGGTA GGCTTGGGTG CTGGAGGGTG TTGCCTGGGG GCGGAGCGAG AAGGAAGAAA 480
GGGCGCTGCT GGTTCACACC TCACCCATGC CCTCCTCTCA GGCCCCAATC AGGATGGAAT 540
TAAAAGACCC TGGGAGGAAA ATAAGGAAAG CAACAAAGGA AATGAGTTCC CCATACAGAA 600
AGGGAAATTG CCTTTCCCGT TAAGGTCAGA CTGGTCCGAA GTAAAGGACT GGTGCGCCTT 660
AGCAACCGCC TCTGCTGAAG CCCTAACGCT GGAGCTCTTT CGCCCTCGCA GAATAACCGG 720
GACTTTCTTG CAGCCGGAAC CAGCCACGTC CTGATTCCAC ACTCCCTTGA GGAGCCAGCC 780
AGCTCCACAT TTACTCAAAG AATCCGAAGG GCACCAAGTG GATGCTCTGC CACACGATTG 840
AAGAGGGCAA GCTGTCTGGG GGGTTTTCCA CCTCTTTTCA ACTCAACTAT TCTGAGCTGA 900
AGTACTGGAC CCGTTTTGTT TTTCCTGTTT TTTCCTGCTT CGGTAAATCT GGAAAAATCC 960
TGCAGGTCTG AAAAACTGTT GGACTTGACA GCGTGTGTGT AGCGCCACCT GGTGACCACA 1020
GCTTATCAAA ACAGCTTCCT TCTGGGGCTC TTGTGGATGT ACATCAAAGG CTCCAGCTTC 1080
CAGACAGGTA CACATCCTGT TCTCACGCCC GGCCCACTTT CCCGTGGGAA TGTCAGCCAC 1140
TCTGATTTGC CTTGGCTGAA AACCTCCTGT CTTTGCATGG AAAAAAACAC AAATAATATG 1200
AACAAGCAAC AGAGTTTTCT TTCTCTCTTA 1230
|
