| Tag | Content |
|---|
EnhancerAtlas ID | HS064-09685 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr21:43888420-43889750 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr21:43889712-43889728 | AGGTTCAAAGTGCACT | + | 6.15 | | RREB1 | MA0073.1 | chr21:43889469-43889489 | GTGGATGTGGTGGTTTGGGT | - | 6.46 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23711 | chr21:43888349-43890143 | Colon_Crypt_1 | | SE_24218 | chr21:43888785-43889542 | Colon_Crypt_2 | | SE_27810 | chr21:43886897-43891053 | Fetal_Intestine | | SE_28739 | chr21:43887048-43891008 | Fetal_Intestine_Large | | SE_50898 | chr21:43888275-43890234 | Sigmoid_Colon | | SE_52661 | chr21:43888347-43890669 | Small_Intestine | | SE_59589 | chr21:43879292-43899707 | Ly3 |
|
| | 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 |
| GH21I042466 | chr21 | 43886847 | 43890842 |
|
Enhancer Sequence | TCTTGCAAGT TTTCTTTAAG TTTAAAATTA TACAAAAATA AATTACAAAA CATCAAAAAC 60
ACTAAAAAGT ACTGAAGTTT TCAAGGACCA ATGGGGTCTT GTCAACCGGA CAAAACAGTG 120
GCATGAAGAA GCTACCACTG GCCAAAGTTG TGTCTGTCTC TGCATCATAA AGAAAAGTGA 180
TTGGAGTGGA TTGAAATGCA TTGACTCAGT GACATCCACA AGCCCATGGT GACTATGCAA 240
AAAAGATCCA GAACAAAGGG ACTTGTCACC TTTGAAGCAT CTGCTAAACT AACACCTCGC 300
TTATAAAATT GGTCATACAA GGGAAAGAAT GAAAGGTTTT ATTCTGTTTT TCTAGGAGGA 360
GCTGCATTTC ATGGGAACCA AATAAATCCA TGATTTACAG CCTAATAAAT TCAGAAGGAA 420
CAGTGGAGTT GGAAAAACAC CATCTCGCAA ACCATACTTG TAGTGGGCTG AATCATGACC 480
GCAAAGATAT CAGGCCCTAA TCGTTATCTG GGGTTAACTA ACAGTGGATC AACCAGATAG 540
GCTATGCCTT AGGCTGTAAT GAAGGAGGAA GTCTGTAACA CCACAAATGT GAATTCCAGC 600
TAAGAACATT ACCGTGAATC CACCAAACCT TTAGCTCCAG CTTCTTTGGC AGTAAGAAGT 660
GCCCAGAGCT TAAAGAACAA GAGAGCCCAG ACAAGCCCAG AAGATGAGAT ATTCTGCCAG 720
GCAGCCCGCC CAGTCCCTTC AAAGCCAGCA ACATGAAAGG GACTGCACTG AATGAAAAGA 780
ATGGGGTGCA GGGATTTCCA TGAAGCTGAC AGCCTCCAGC TTCAGACTCT GCACAGGCAC 840
AGGCCCCTTG CAAGGTCCAG ACAGGGTGTC CACCTGGCCC TGTGTTTCAT CTATTTTGCA 900
TTAGTGAAGG ATTTTAACCA TAATCGTGCC TCTGCCACTT TCCCCTCTAA TTTCAATCAG 960
ACATGTGTCC CCTCAGGTGG AAGGGCATTG AAGTGGCCAC AGGCACTTTT AGAATCTGTT 1020
TCAGGGGCAC TAATTGAATT GAATCAAGGG TGGATGTGGT GGTTTGGGTT CCAGAGAGTA 1080
TTTGTGTATG CCACTGGTTT GCAGTAATTT TCATATGTAG TACAGTTTCT GCCACCTGTC 1140
CTGGAGTAGT ATCACTTCCA GAAATACTTC TAACACTCAT TTTGCTACTT ACCTAGAATT 1200
GAGACACGTA AGTGCAGGGT CAAACTTCAA ATCCCAGTAT GAACCTGTCC TCCAGCTCCA 1260
GCACCATTGC GTGTGGGAGT GCAGAAGAAA TTAGGTTCAA AGTGCACTGA GTCAGAAGCT 1320
GGGCTATGGA 1330
|
