| Tag | Content |
|---|
EnhancerAtlas ID | HS147-04643 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:218885150-218886580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr1:218885610-218885621 | TGGGTGTGGCT | - | 6.14 | | RUNX1 | MA0002.2 | chr1:218886134-218886145 | AAACCACAAAC | - | 6.02 |
|
| | 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 |
| GH01I218710 | chr1 | 218883954 | 218886752 |
|
Enhancer Sequence | ATATATTTGT CTCCCTCAGC AGAATTGAGT TCTTCTAGAG TGGATACCCT GCCTGCCTTA 60
TTCACAACTG GGTCTCCAAC ACCTAGAAAA ATTTCTGGTA TACAGCAGGC ACTCAATTAA 120
TGTGGCTTGA TTAGATAAAT CAGGACAATC ACTGTCTTCA AGAAGATTAA AGTCCAGTGG 180
AGGAGAAAGA TATGTAAGCA CAATGAAGTG TGGTAAGTTC TGTGACACAG GAAATCATAA 240
AACTATATGT CAACAAACAG AGGGTGGGCG TGAGGGAGGA GTGAATAAGG CTTCCAAAAG 300
ATGATGCAAT GTGGGACATT AATGGATGAA CGGAACATTG CCCATTTGTG CCATGGTTCT 360
CCTCCCCTAT TCTTCTCTTT GAGGATTCTA GATTTCATGT GTTCTCTTTT GATGGCTTGG 420
GACAATGGGC AGAGATGAGC ACTCTGGGCC TGCTGTGTCC TGGGTGTGGC TGTGTGGGTC 480
TTTCTGTAGC TGTGCCAGGG GAATGACTTT ACAGGATCTC AGCAACAAGC CCAGGGTACT 540
GTAGCTTGTG GGATCTTGGC AGAACTGTCT CAGTGCTAAG GTCAGAATTG GGGAAAGATG 600
TTGTAATTGC CTTAAAGGCA CGTGGACTCA AAGGCAACGC GGACACTGAA CACAGCTCCT 660
TTCGCAGACT GCACTTGCAG GGAAGTGAAT GGGAGCTTTT CCCATGTGTG GCCAAATCGA 720
TGGGGTTAAA TATGATTAAG CCCAAACATG TAAAAACAAA ATTCCCAAGT TAATGGTGAT 780
GTAATATTCT GTTAGGGTTA GGCCAGATTA TAGCTGATTG CGTTGCTTCA TATTGGAACC 840
TGGTCAAAAC GTTGATTCCT GTTATAAATC CTGTAGTCAT CCCCAGGAAT AGCATTATCC 900
ACCAAAAAAA AAAAAAAAAA AAAAAAAGGC CTTTCTAAAG TTTCTAGAGA GTTTCAATGA 960
GAAATTTCTT AGCAACACCT GGAAAAACCA CAAACAACAC AACCGGCTGT TGGGGAGCCC 1020
CAGGAAAATG CCACACATCT AGAGTAGGGA GCCTGCTGTG CCCTTCTCAG GCATCCTAAG 1080
AGCGCAGGCC TGGGTTGAAT GTGCTCTACC CCACATCCTA ACAGGGAAGA AAAGCACGAG 1140
GCCATTAAAC AAAAAGGAAA AATAATACCA CACGTCGCTG AAATCACATC CAACTGGGGC 1200
CAGGGCTTGA TCTGCAATTC TTCATCCTTT CTGGTCTTCA TTCAGCAGCC ACTGACACCC 1260
CCACAGGATG GATTCTTTTT CCAAGGCAAC AAATGCTCAA TTCATCAGGG AACCAAAGCA 1320
CAGCTCCTGT GCAATTTGTC CAGGATCCTT ACAAACATTG AATATAAATG GAAACCAAAG 1380
ACATATTATT TTCGGAAGTG AACATATTTT CACCCTAGTT TAGGATGTTG 1430
|
