| Tag | Content |
|---|
EnhancerAtlas ID | HS038-19448 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr6:167679320-167682010 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr6:167679981-167679992 | GACAGCTGCTG | + | 6.14 | | Tcf12 | MA0521.1 | chr6:167679981-167679992 | GACAGCTGCTG | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28100 | chr6:167678541-167683235 | Fetal_Intestine | | SE_29209 | chr6:167678588-167683255 | Fetal_Intestine_Large |
|
| | 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 |
| GH06I167265 | chr6 | 167678859 | 167683111 |
|
Enhancer Sequence | GTGGGGTGCT GGGTCTGAGA CAGCTGAAGC TGTGTTTATC AACGCACTGT TCGTAGCATC 60
ACTATTCTCA GGGGGTAGGC ATTTTTATCA GGAAACTTCT ATTTCTAGTG GGAGTAATTT 120
CGGAAAACAG GACAGAGAGA TTCAGGCTGA ACAGAAAATT TCCAGGGTTC CTCTGACCCT 180
GCCCCGCAGA TGGCTCCTGG GAAAGGCTGA TTAATCAGCT GGGTCCGGAC TTCTTAAGTC 240
TAAAATATGA TGATTTTAAG TCAAGCATGG GATTAGAACA GTGGTTATCA GCCATGGAGG 300
TAATTGCGCC TGTCTCAGGT TCTTGGGAAG GGAAGGGAAT CACTCATCCC TGACGGCTTC 360
CTGGGCTGCC CCTGGGCAGA GGCTGGAAGA GCTTGCGTTC TCTGGGCCAC ATTGCTAAGA 420
TTAATAACAC GTATGGACAC AGTGCAGGGC CTGTGGGATT TTTCACTTAC TCCCCACCAC 480
TGACAGCCTC AGTTCCGTGT CTGAAGACCG TGTGCCACCC TCCCTGACTC TGAAGAGCCT 540
TGCACCAGGT TCACAGGCTC CTGGAGACAC TGAAGTCTGA CCTGGTCGCC AAGCCACTCC 600
CTGAAGGAGC AGAGTGAGCT CCAGCCCCAC TGCCCATTAG CAAATCGAAG TGGGGAACAA 660
AGACAGCTGC TGGGGGACTT GGGCAAATGG CCTGTTTCTG TCCAGCGTAG CCTGGGTGAT 720
CACTCACAGT GGCGACTTCC TTTGCCTTAA TCAGTCAGTG GAGCCATCGC TGACGTTCTT 780
GCCTTTTCTT TCTTGCAGGA CGTTGACAAA GGAACGCACG CTGACACTCC CACATGAACA 840
GCTGGCTGCT TCCCAGCGTC CTACGGGAGA GCTACCGGCT TCTAGGCAAT GCTGCGTGTG 900
ATCTGTGGGG GAGCCTGGCC ACTCCTGGAG GTTCCAAGGT CAAAGAAACG CATTCCGGAT 960
GCGACGGATT TGATCTTGGA AAGCTGCTTT GAAGATACGA TAGCTATTCC CTATTGTTCA 1020
CTTTAAGGCA AACAATGTAT ACATTTTTCT GTGTCAGGCT CCTCTGTGAA GTTAGTGAAA 1080
CGGTAGCTTA GTTTGCTCCC ATCTCCTGTT CCGCGCTGCT GGTTTTCGAT TGTGCGTCAC 1140
TGAATTGCCA TCAGAAGTCC AGTCCCGACT GCGTGTGCGA GGCCAGGGAG GGAGGTGAGA 1200
GGCGGCCTCT CGGACACACT CTGCTGTGAT CTTTGATTCA GGAGACACCC TCTTTGTTGA 1260
TGATCCCTAA GAACTAAAGA GAGACTCCAG CATCACCCTT TCTCCTGGTG CCCTGTCCAT 1320
AACTAAGCAT CCAGGAATGT CCTCTGCAGG CATTTTCTCT GCTCATCCTC GCAGCAATCC 1380
TGTGAAGGAG ACGTTTTCTC CATTCTATAG GAGAGGACTC TGAGGTTCAG AAAACTCAAG 1440
TCAGAGAACA CGTGAGCTTG GACTCCGTTG CCTGACCCGC GTCGGACTGT AGGCTGCTGT 1500
TGCAGCTGTG TGGCTTTGGG TGCCTGGCCT GGGTGCTATG TGTTCACAAA ATGCACTTCC 1560
CTTCCACCCT AGGTTCAAGG TGAACTCCGA TCCCAGCCTC TCCTGTCAGG CTCAGCAATG 1620
GAAATGAGCA GAGGGGCCCT TTGTTCCATG CAGGCTGAAT CCAGAACCTT CTGAGGACTT 1680
GAAGCCCTTT TATGCGGACA GGATGGGAAG TTAAGCGAAA GTTAACTTCT GTTGGATTAA 1740
GACCCTGAAG ATTGGGCTTT AACACCTGTT GTGTTACCTG CACTCAAACA AACCAGGGCT 1800
CCTTACTCAG CCCTCAGGAG CCTTGGCATT CTCACCTCTA AAGCAGGAGG AGTCGTGATA 1860
ACTGCCTTGA GGAATTTGAG CAAAGTTAAA TGACCTGAAC TATTTGGGCG TGTCTTGACC 1920
AATGTCCGAC CTTGGGAGGT GCTGGATGAA TTTTTATTTC TCTACTTTAA GTCAGCCTTT 1980
CTACCTTGTT GCTCTTCTCA GCTGCCTTTC TCTGAGCCTC CTTCATCACT CTGTTCATTT 2040
CTGTGAGACA AAGATCATTA CAACTGCCTT AATATTTCGG TGCAAGACGC ACCGTGACCT 2100
GACATTGCTC TACCCCGCCT CCTGCCACGA TCATTCTTTT GTAGCAATAT TCCGCCAGCT 2160
TCATTTTGTG CAGTGAGTGG AACAAGAGTC AGAACACCAG GGCGGCTGAG CCTGTCGATC 2220
AAGCCTCCAC CTAACAACAG ACATGCCTGA GTCCCACAGT CATAATTAGG ATGAAGCTTT 2280
TCCCTGGCTG GACCCGGACT GCAGTCACAC TGTAAGAGCT CATCATTCTA GGCCTCTGCC 2340
AGTGCGTGTT CAGTCAGAGG CAAGCAGTGG CCCCGGCTCC CAGAAGCATG GGGAGGACTC 2400
CTACCAGGGA CGGTGGCCAG AATGGCTGCA CACAGCCTTT GCTTCCAAGA AAAAGCATCT 2460
CCGCAGGCCC AGGCACCTCT GGCAGCCCTC AGAGCAGGAC CCTCTTCAAC AAGGTGATAG 2520
CAGAAGGGAA GAAACGCAGA GGTCTGTCTC AGAGATTAGA GCAACACAGA AACTGGATGC 2580
CCCCTTTCAG GGGAGAAACA CGGGGTTTCA CATCAGGAAC CTGTTGAGGA ACTTCCCGTC 2640
AGGCCCAGCA ACACACCCAG GACCAAACCC CAACAGTGAT GACTAAAAAA 2690
|
