| Tag | Content |
|---|
EnhancerAtlas ID | HS098-03145 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:117016960-117018710 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr1:117017850-117017860 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr1:117017850-117017860 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr1:117017850-117017860 | AATGGAAAAT | - | 6.02 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_27848 | chr1:117013898-117021408 | Fetal_Intestine | | SE_28774 | chr1:117013873-117021547 | Fetal_Intestine_Large | | SE_41250 | chr1:117016870-117021350 | Left_Ventricle | | SE_47846 | chr1:117017467-117019346 | Pancreas | | SE_50584 | chr1:117016337-117019459 | Sigmoid_Colon | | SE_52493 | chr1:117016317-117021272 | 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 |
| GH01I116471 | chr1 | 117014027 | 117021401 |
|
Enhancer Sequence | CTGGAGGGAA CAAGGGGACA AAAAAGGCAA GCTGACATCA ACCCCAAACC CCAATAATTC 60
GGAGGAGAGT ATCCCTGGTA ACAGAAACAG AGACAGAAGG AGGTCTGCGG GAAGAAAGAT 120
GAGTTCTTTA TGTATGCCAA TTTTCACATG TTAAACATGC CATGCCTTCT ATCCGTGGAG 180
CCTTCACATA CAAGACACTA TGTGCGATAT TTACAAAAGC CCTAACCCGA TTGCCTTTTT 240
ATAGATGAAG AAATTGATAT GCAGAGAAAC AAAATAATTT GGCTTAGGTC ACATAGCTAG 300
GAAGTGGCAG AACTAGAAAG TGGCAGAGGT GGGCCCTCTT GATTCAAAAG ACACTGAATC 360
AATGTGTAGT CTAGCTTAGA AGTCCTCGGC CTGAAGATAA AGATGAAGGA AATGAGATAA 420
AGGGAATGAG GCCAAGAAAC AGTGAGGCAG ATGGAGAGAA GGGAAAGAGA GGTACAAAGG 480
TAGTGGAGGA TGCACCCTAA TAACTCCTCA CAGATAAAGC AATACAGCTA CTGCGACCAG 540
CTATCAATGC AGTTCATAAA TGCAGAGATC ATCAGAGCAG GAAAGGACCT CTGTGCTCCC 600
AGCCTCCCCG TGTTACAGCT GAGGAGTAGA GGGCCAAGGC ATCTAGTGGC TTCCCCAAGG 660
TTCTCCAGGC TGCTGTGGAG GCAGAGCCAT GGCCACGGCC CTGGCCTCCT GGCACTCAGG 720
CCTAACAGCT TCCATCAGGC TGTACCACTG AGATTATCAT CATCAGTGAT GATGGTGCCA 780
TTAACAGCCA TGGCCACCAC TATCTGGTTT TTTAGCACCA GCCACCCTGG CAGCCATCTT 840
CATTTTGTGA CTTGAAGAAA GCACTGCCCT GGTCATGTGA GCACAAGAGG AATGGAAAAT 900
TCCAGGTCAG GGAACAACAC ACCCTCCAGG CATCCTTCTC CACCAGCCCT GCCTTCAGAG 960
GCACCAGGCC CTTTTGTCCC ACCACCAGTT AATATTTCAC TTGGGTGAGA CTTTAGAGAA 1020
CAAAGAACAC AAAGCTGGCC TTGAGGGGCC AAAGGTAAGC AGCCCATGGT TCCCGATTCG 1080
GCTCATAAAT AAGAACAGGG CAAATGTACT TTGGATAAGG ACGCGCTCAG CCTCCCGCAG 1140
AACAGCTGGG GAAGCTATTC ATAGGAAAGC GTGCTATTTG CGTCTGCCTG GCATTTGAAT 1200
GAGGCTCACC TAACTGTGCC TGCCCTCCCC ACAGATGTGA GTCACGCTCC CCACTCACGA 1260
GTGAGGAGTG GCCAGGGGCA AAGGAGAATT GCTTCTCGGC TCAGCTGAGA GAACTGTGGG 1320
GGCCAGGAGC GGCACTGCCA AGGATATCTC CCTCCCCCGG GCAGGGAGGG CCTCCAACTG 1380
AGGACACTTA TTCTGTAGTG ATAGAGCCTG ATTCCCCTCC ATGTGAGAGA GGTGCCTCCT 1440
TGGACCCTGC TACTTTGTCC CTTGGCCCTT GGTCAAGCAA AGGGGACAAT TCTCAGCCCC 1500
CAACCCCTTG CCGGTGGCTT TGACTATCTT CTCACATCTC CAGTACTCGG GGAAAGCCAG 1560
TCAGAGCAGC GTGGGAGGCC AGTTCTAGTG TCACGCTGCC ATCCTCCAAG TTCTACTGGT 1620
CCCTGGTCTC TAATTGCAAA GCTTACGTGC TGTGGAGGTG AAGTGGGGGT GATCCCTCCC 1680
CCTTAAGCAG CACTGCCCAC TTCTGAAGGT CATCCACCAA TGCTCCTGCC TCCTGTAGCA 1740
TCCAGTGAAG 1750
|
