| Tag | Content |
|---|
EnhancerAtlas ID | HS078-01683 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr1:185393710-185395370 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELF5 | MA0136.2 | chr1:185394856-185394867 | ACCAGGAAGTA | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 185394174 | 185394315 | | chr1 | 185394811 | 185394863 | | chr1 | 185395136 | 185395232 |
|
Enhancer Sequence | TGTCAGTTAT AAGCCACACT CCTATTTCAG AAGTGAAAAT TATGCATCAT AGAATGGAGG 60
AAATATGTGG CTTCTTTCTG TTCCATGGCA ATGGCAGGAG TTTCAAAAAC TGTTTCTGAG 120
GGGAGAGTCA CTTTCTGCAT GGTGTACATG ATGATCAAGC TGGAATCCTA CACTTGGCTG 180
GGCAGTCATA GGAGCACCAC GATACTATCC AGGCAACCCC ATTAGCCATC TTCCGGCTGA 240
GGGGAGTCAA ATACTCTACC GTCTAATCTT CATTGCCTTG GTGGCTTCAC ATGCCTTATT 300
CCCTTTCCAT ATGGTGTTGA CAGAAACTGC AGAATGTGTA GACAAAGGGT AGCATAGGTG 360
TGAGGCTGCA TGAAATGAAT GTTGATATTT TGAAACGAGA AAGATGGGTT CTTCCTATTA 420
GGAGAAATCC ACATTAAAGA GAAGAGCACA GGCAAGCTTG GAACTAAAAG GGAGAAGTCA 480
GCTTGAGAGT AGGGTAGGGG AAGAGTGAAG AGCGGAGGGC CAGCTCTGTC GCCTGGCTTG 540
GTTATGGTGG AAAAGACTGC ATTTGGCAGA ACACATAATC AATGACGGAT TTTTCATTTT 600
TATTTAAACT TTGGCTTATA GAAGCGATTT CCTTTTTCTT CCTCACTGGT TTCCAGCCCT 660
GAGCCTCTAC CCAGCTATCA GCAGGAGGGA GTCCCCGCAC AAATGCCTGG TATTGGTGAT 720
AGATCTGTGT TAATTGTATC CATACTGTCC TACCCAGTCT TTCTTGTAAT TATGGGCAAG 780
AAATTCTAAG ACAGATGGTT AGCTTTCTCC ATGTGCTGTG TGACCATGGA AATGAGCAAA 840
GCTCATGAAC TGACAGGAGG CCTGAGAGGG GGCTATTGTC TCATTAGCAC TCAGTTCTAT 900
CTGATTGGGT TGATGCTGCA AAGGTAATTT AATGTGTCAG AGCAAACATG TGGCAAGACC 960
AGTACCTATG AGAGAAGCAT TGCATTTTTA AAAGCCTGAA GTATGAAAGA GATTTTTTAA 1020
GTGTCTAGAA GTCAGGAAAA ACTTTAGTCT CTTAAACTAG ATAGCACCTT GGTGACTTTA 1080
CTCTCAGCTT AAGGTGCATA GACAAATTTA AACAGGACTC TCCATGTTTC CTGGAACCTA 1140
AAATTCACCA GGAAGTAATT AGCATTTACA GACAAATAAT GCTTCAAGAG ACCTGTGAGA 1200
TAAAATACAT GTTTGGATTT ATGGAAAATA ACAAAATATC ACAACACTCT CAGAAAAAAA 1260
ATTGTATTGA AGACTTAATA ACTACAGAAA GAAAAACAAC TAGTATTATT GAGCATCTAC 1320
AATCTGCTGA GACCTTTATA TACATTTCTC ACTTTAACCT CAGTACAACC TTGGAGGTAG 1380
GCTTGATCTA TATTTTGTAG AGTAAAATAA TCAGGCTCAG AGTATTTAAG TAACTATCAA 1440
GGTCTGAAGC CTGGCGAGTT GTGGAACTGA TGTCTGACAC TTCCCATCAC ACCAGATACC 1500
TACTGCCTTT AGCCACACTG AGATAAAATA GAAGCAACTG AAATTCCCTA GGTTCCATCT 1560
AGCCTTGCTG CTCTAACCTC CTTCTCTCTT AAACTCCCAC ACTGGCCCTT TCCTATGGAA 1620
TCATATGTTG ACTGAACACA TACTGCTTTG TGATGGGTTT 1660
|
