| Tag | Content |
|---|
EnhancerAtlas ID | HS003-26345 | Organism | Homo sapiens | Tissue/cell | A549 | Coordinate | chr2:97330040-97331880 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr2:97330587-97330598 | TTCTTATCTTC | + | 6.02 | | TFAP4 | MA0691.1 | chr2:97330789-97330799 | ATCAGCTGTT | - | 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 |
| GH02I096664 | chr2 | 97330129 | 97332421 |
| Enhancer Sequence | GTTGCCTAAT GCCTCTTGGG AATCCCTCCC TGTGATTCCT ATTCCACCCC CTCCCATCCC 60
CAGGCAACCA ACAATCTGCT TTCTGTTACT ACGTATTAGC TTGCATTTCC TAGTGTTTCA 120
TAGAAATGGA ATCGTTCAGT AAGTACCCTT ATTTGTCTGA CTTCTTTCAC TCAGCATAAT 180
TATTGTGAAA TTCATTCATG CCATTGCTGT GTATCAGTGG TTTATTCCTT TTTGTTGCTA 240
AGTAATATTC CATTGTATGG ATGTACCACA GTTTGCTTAT CCCTTTCCTT GTTTATGAAC 300
ATTTCCGGTT TGGGGCTGTT ACAATGAAGC TGTAAACACT TGTGTACAAC CCTTAGCATA 360
GACATATGCT TTCATTTCTC TTAGGTAAAT ATGTAGATGC AGAATGACTA GATTCTATGG 420
TAGATGTATT AAGCAATGAG TGGGTCATAC AACTGAACTT TCCAGAGAAC TTAAATGTGC 480
CCTTTCACCC ACATATAAAA ACAAAACAAA TCCCTTTAAA GACACATTTT AAATGATAAT 540
ATACATTTTC TTATCTTCTC AGCAACTTTG CCCTGAATAT AATTAGAGCT TTTTGTTGAT 600
GGCCTGGAGC CATTATGGGA ACATAGTTAT TATCCTGGGC TATCTGCAGT ACCGGGCTAC 660
TTGTTCCTGC ACTAAATGGC TCTGAGATGC TTTCTTTTTG GGGTTCTGTA GTCTGATTTT 720
GATCGCCTTT CAATCTGTCT CCGTCACCTA TCAGCTGTTG TGGATGACAG TTCTCTTGAA 780
GGCGGAGTCT TACTGGCCTT TTGACTCTAA GTCAGGCTTC TAAGAGCAGT GTGTAAAATA 840
AGAACACAGT TCTGAGAGAG AACTTGAGCT GAGAGATAAC TTGAGCTCTC TCATAAGTGC 900
AGGCACACAG GAATTTGTGT GACATGGACT TGGCAACCCA GAGAATGTTT TGTTTCCTCA 960
TACCTTACAT TGTGAAATAC AAAATTAGCT AATGCGCTCC CCTTCTCCCT CCTGTGAACT 1020
CCCCTCCTTG CTGCTTCTAG TAGCTACCCA GTCTGCCTTC CTGTGAGTCA TCACTTTCAA 1080
CCATTCCTCA TAATCCCTGC CTCCTTGGAT GATTTTATAG ACTCTGAAAG TAGGAAGACA 1140
TTTCAGAGGA GGCCTAGTCC ATCCCCCATC CTTGCCAAGC TCCCTCCCAC CTTTTCCGGC 1200
CTGTGATGAG GGCACAGGGC TGGGATCCTC AGATGTTCTG TGGCTGTTCA GAGCCTTGGG 1260
AAATCTTCTT TTTTCATCTT CTGTTCATCT TCTTTGTTCA TCTTTTTTTT TTTTTTCTGA 1320
GACAGAGTTT CATTCTTGTC ACCCAGGCTG GAGTGCAATG GCGCGATCTC GGCTCACTGC 1380
AACTTCTGCC TCCTGGGTTT AAGCTATGAG TAGCTGGGGC TACAGGTGCC TACCACCAAG 1440
CCTGGCTAAT TTTCATATTT TTAGTAGAGA CGAGGTTTCA CCATGTTGGC CAGGCTGGTC 1500
TCGAACACCT GACCTCAGGT GATCCACCTG CCTTGGCCTC CTACAGTGCT GGGATTACAG 1560
GTGTGAGCCA CCATGCCCGG CCCTGTTCAT CTTCTTACAG GCTCAGAACC AATGGCACAG 1620
GCCAGGCCCT CCCTCATCCC TGAGAGAGGC CTTCCAACAT TTGAAGATGT TCAAACACCC 1680
CTGGAACCTC ATCCATTTTC CCCAGAACAC AGTCTCCAGG GTGGGGCCCT TTGGATACTG 1740
GCCTGATTGC CTTTAGCCCT TTGGAAATGC AGCAGGCAGG TGTGAACCTC TCTCTGAAGA 1800
GGCAGAACAG CCAGCCACAC AGATGGCAGC ATCTGAGGCC 1840
|
| |
|
|
|
