| Tag | Content |
|---|
EnhancerAtlas ID | HS063-04064 |
Organism | Homo sapiens |
Tissue/cell | GM18505 |
Coordinate | chr20:48284760-48286230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr20:48285127-48285147 | TGGGTGGGGGTGGGGGGGGC | - | 6.45 | | ZNF740 | MA0753.2 | chr20:48285136-48285149 | GTGGGGGGGGCGT | - | 7.12 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_09853 | chr20:48284482-48285944 | CD14 | | SE_09853 | chr20:48286067-48287758 | CD14 | | SE_27783 | chr20:48284024-48299682 | Fetal_Intestine | | SE_28728 | chr20:48283919-48299710 | Fetal_Intestine_Large | | SE_53007 | chr20:48284731-48286040 | Small_Intestine | | SE_58419 | chr20:48273398-48331383 | Ly1 | | SE_59165 | chr20:48284219-48322551 | Ly3 | | SE_60613 | chr20:48275063-48331415 | DHL6 |
|
| | 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 |
| GH20I049667 | chr20 | 48284130 | 48287655 |
|
Enhancer Sequence | CTATTAAAAA AATCCAAGTG GTAAAAATTA ACAGCTATGA AGTACCCTAT AAACATTTCC 60
ACTGACCTAT TAGTCTACCA TCTGTTAAAT TATTAAACTG TACATAAGAT TAGACATGAA 120
AATGCTGTCT AAACAGATAC TAGATGGCTG GGTAGCCTAT GGTAAGTACT TTACTGATCT 180
AAGCTTCAGC TTTGCTTCCC CCAAAATTCT TAATAGCATG ACCAGTTATC AACCCTCAGA 240
AGTACCAATA TCCACATGCA CAGCCACATA ACCTCAGTAT AAGCTTGGGT GGGAGAAAAC 300
TGTAAATTAC CTTGCTGGTT CCATTGAAAC TGAACACGTA CACTTATCAA AACAACCCTG 360
CGGAGAATGG GTGGGGGTGG GGGGGGCGTC AGGGTATGAC GGATGTTGCT GATGGGAATG 420
TGCTAGAGGC ACAAGACCAG CACTGCCACA CTCCTCTGTG GAACTGAAAC CAGAACAAAG 480
GCTCTGCTCC CCTCACCTCC GCACCCCCTC GTCCTAATCT CTGTCCGTCA CCGCCCCCAC 540
TCCACCGACC AATCCCTGTC CCTGAATTGC CTTGTGGTTC CAGCCTCCCA CCCCCACTGA 600
CACCTCCTCT GTATGAACGT GCTTTTGTGA CACCCGCTCA TACTAAGCTT TTTTTTTAGA 660
CAGTGTCTCG TCCTGTCACC CAGGCTGGAT TGCAGTGGCA CAAACACAGC TCACTGCAAC 720
CTCAACTTCC TTGGCTCAAG CAATCCTCCT GCCTCAGCCT CCTGTGTAGC TGGGACCACA 780
GGCGTACACC ACCACATCTG GTGAATTTTT TTATTTTTGT AGAGGTAGAA TCTCACTTTG 840
TTGCCCAGGC TGGTCTCAAA CTCCTGGGCT CAAGCAATCC TCCTGCCTCA GCCTCCCAAA 900
CTGCTGGGAT TACATGTGAG AGCCATCATG CCCAGCCAAT ACTAAGCTTT AATGTCCCTT 960
TCCTAGCTTT TCCTGGTATC ATCCCACCCC CAAGATTAGA ACTGCCTACA CCTATCTTTG 1020
GGCTCTTTCT CAACTGATAC ACCAACTTCT ATCCATGACC TCTACAAATT TGAGCATGTC 1080
TCTCTCTTCC AATAGACTGT AAGCTCCTTA AGAGTACAGA CAGTCTTATT CTTTTCTTCA 1140
TCAACTTCTG ATAAATAGTA GGCATTTAGC TATTTATTAA AGAATTACAT AGGCTGGGCG 1200
TGGTTGCTCA CACCTGTAAT CCCAGCACTT TGGGAGGCTG AGGCAGGTGG ATCACCTGAG 1260
GTCAGGAGTT CGCAACCAAC CTGACCAACA TGGAGAAACA CCGTCTCTAC TAAAAATACA 1320
AAATCAGCCG AGCATGGTGG TGCATGCCTG TAATCCCAGT TACTCGGGAG GCTGAGAAAG 1380
GAGAATCACT TGAACCTGGG AGGCGGATGT TGCAGTGAGC TAAGATCGCG CCATTGCACT 1440
CCAGCCTGGG CAACAAGAGC GAAACTCCAC 1470
|
