| Tag | Content |
|---|
EnhancerAtlas ID | HS095-16621 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr2:97330350-97332500 | 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 | TGGGGCTGTT ACAATGAAGC TGTAAACACT TGTGTACAAC CCTTAGCATA GACATATGCT 60
TTCATTTCTC TTAGGTAAAT ATGTAGATGC AGAATGACTA GATTCTATGG TAGATGTATT 120
AAGCAATGAG TGGGTCATAC AACTGAACTT TCCAGAGAAC TTAAATGTGC CCTTTCACCC 180
ACATATAAAA ACAAAACAAA TCCCTTTAAA GACACATTTT AAATGATAAT ATACATTTTC 240
TTATCTTCTC AGCAACTTTG CCCTGAATAT AATTAGAGCT TTTTGTTGAT GGCCTGGAGC 300
CATTATGGGA ACATAGTTAT TATCCTGGGC TATCTGCAGT ACCGGGCTAC TTGTTCCTGC 360
ACTAAATGGC TCTGAGATGC TTTCTTTTTG GGGTTCTGTA GTCTGATTTT GATCGCCTTT 420
CAATCTGTCT CCGTCACCTA TCAGCTGTTG TGGATGACAG TTCTCTTGAA GGCGGAGTCT 480
TACTGGCCTT TTGACTCTAA GTCAGGCTTC TAAGAGCAGT GTGTAAAATA AGAACACAGT 540
TCTGAGAGAG AACTTGAGCT GAGAGATAAC TTGAGCTCTC TCATAAGTGC AGGCACACAG 600
GAATTTGTGT GACATGGACT TGGCAACCCA GAGAATGTTT TGTTTCCTCA TACCTTACAT 660
TGTGAAATAC AAAATTAGCT AATGCGCTCC CCTTCTCCCT CCTGTGAACT CCCCTCCTTG 720
CTGCTTCTAG TAGCTACCCA GTCTGCCTTC CTGTGAGTCA TCACTTTCAA CCATTCCTCA 780
TAATCCCTGC CTCCTTGGAT GATTTTATAG ACTCTGAAAG TAGGAAGACA TTTCAGAGGA 840
GGCCTAGTCC ATCCCCCATC CTTGCCAAGC TCCCTCCCAC CTTTTCCGGC CTGTGATGAG 900
GGCACAGGGC TGGGATCCTC AGATGTTCTG TGGCTGTTCA GAGCCTTGGG AAATCTTCTT 960
TTTTCATCTT CTGTTCATCT TCTTTGTTCA TCTTTTTTTT TTTTTTCTGA GACAGAGTTT 1020
CATTCTTGTC ACCCAGGCTG GAGTGCAATG GCGCGATCTC GGCTCACTGC AACTTCTGCC 1080
TCCTGGGTTT AAGCTATGAG TAGCTGGGGC TACAGGTGCC TACCACCAAG CCTGGCTAAT 1140
TTTCATATTT TTAGTAGAGA CGAGGTTTCA CCATGTTGGC CAGGCTGGTC TCGAACACCT 1200
GACCTCAGGT GATCCACCTG CCTTGGCCTC CTACAGTGCT GGGATTACAG GTGTGAGCCA 1260
CCATGCCCGG CCCTGTTCAT CTTCTTACAG GCTCAGAACC AATGGCACAG GCCAGGCCCT 1320
CCCTCATCCC TGAGAGAGGC CTTCCAACAT TTGAAGATGT TCAAACACCC CTGGAACCTC 1380
ATCCATTTTC CCCAGAACAC AGTCTCCAGG GTGGGGCCCT TTGGATACTG GCCTGATTGC 1440
CTTTAGCCCT TTGGAAATGC AGCAGGCAGG TGTGAACCTC TCTCTGAAGA GGCAGAACAG 1500
CCAGCCACAC AGATGGCAGC ATCTGAGGCC AGGTGGTCAG AAGGGGAGCA GAGCCCAGGG 1560
CACTGCAGAA AACTGGCCTG TACCAATGGT CAGTCCGAGG GCCCCAGGGC AGAAGGGGAG 1620
GCAGCACACT AGATGAGGAA CCAAGAAGCA GGAGGAGAAT TATTAGCAGG ATGGATGGAA 1680
AGGTGGTTCC GCCATAAATC TGAACTTGGA GGACTCCTAA CTTTGGAAGA CCTGGATGCC 1740
TTCTGGTGCC GATCTCTCCC CTTCCAATGT CCTTCCTTAA CCTGGGCAAT TTCCTCCTTT 1800
CTTACTGACT AGCTGCTCAC CTGGAAAGCC CTTTCCTCTT CTCCTTGGCC CCTTAGCTGT 1860
CAGGACCCAG GGAGAATGGG ATGAAGAAAA TGGAAAGCTG GGAGGTTCCC AGCCACATCC 1920
CAAGAACTGC TGTAAGGAGA AGAGGCCCCA GCTGAGAGGA TTGAGGATTT GGGGTCCCAC 1980
TCTGGCCTCA ACCCAGCAGC TCTATTTTAC ACATGGACAC ATGGATTTTT TTCTTTTATT 2040
TATTTATTTT TTTTTTTTAG ACAGTCTTGC TCTGTTGCCC AGGCTAGACT GCAGTGACGC 2100
AATCTCAGCT CACTGCAACC TCCACCTCCT GGGTTCAAGC AATTCTTGTG 2150
|
| |
|
|
|
