| Tag | Content |
|---|
EnhancerAtlas ID | HS148-08972 | Organism | Homo sapiens | Tissue/cell | NHLF | Coordinate | chr2:1048040-1048950 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat6 | MA0520.1 | chr2:1048190-1048205 | TTCTTCCAGAGAACT | + | 6.49 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 1048423 | 1048539 | | chr2 | 1048542 | 1048896 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I001052 | chr2 | 1048190 | 1049134 |
| Enhancer Sequence | TAAAGAGTTC ATCCTTTGTA CACAAATCAC AAACTGTAAG GTAAAACATT CTTGCTATTT 60
TCTTGTGTGC TTTTCATATC TGCGGGACTC ATAGTGGCTT CCCCCTTTCC TCATCTGGCT 120
GCTTCTGTGT GTTCTCTCCT TATTTCTCAC TTCTTCCAGA GAACTGTTCT TTGGCTTTGT 180
TCATTAGTTG ATTTGTCTTC TGTTTCATGT ATTTCTGCTC TTATTTCCTT TATTCTCTTT 240
CCTTTTTCTT GCTTTGCTTT TGGAAACTGA AATCAGAGGT CTCTAAAGTG TTTTGAAAGC 300
CACATGGTAC CTTAGGATCA CTGGCCATGT CGTCCTTTAT AGACAATTCT GCCATCCTTT 360
CGTGGAAGCA GGTGAAGGGC CGTGGCTGTG TTCCAATAAA ACTTGATTTA CAGACACAGG 420
CGGTGGACCT GAATGCTGGG TGGCCTACCC TGGGATGAGG TCGCTGATTT TCACCTTTAG 480
TTTCTGCATG CATTCCAGCT GTAAGTTATT CAGTTGCAGC TGCACTTCAC AGGTTTTGAA 540
AGTCGTAAGC TCACAATCTG TTCAAAACAC GTTCCAGTTT CCACTGCGAG TCCCCTCCTG 600
GATCTGTGGT GATTTGTGAG TATGTTGCTA AACTTTTCAG GAGCGGAGAT TTTCTGTTAT 660
CTTTTTCTGG TAGTTTTCCA TTGCCACATA TGTGAAAATA ACATACTCTG ACTTCAGTCC 720
TTTGAGATTT TTGAGGTTTT CTTTATGACC CTGCGTTTTG TCCACGTAGG AAGGAGGGTG 780
TTCTGCTGTT GCTGAGCACA GTGTTCAACA GACATCAGTC AGCTTCCATT CCTTCACTGT 840
GCTTTTCAGA TCAGTGCAAT GCTGATTTGT TCATGCTTCT AAAATGTAGG TAAGCAGGCT 900
TATTTTTAAT 910
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