| Tag | Content |
|---|
EnhancerAtlas ID | HS060-19696 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr2:96350330-96351790 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr2:96350799-96350812 | GAATGTTCTGGAA | - | 6.62 | | NR2C2 | MA0504.1 | chr2:96351455-96351470 | GGAGGGCAGAGTTCA | + | 6.03 | | ZNF263 | MA0528.1 | chr2:96350398-96350419 | GAAGGAGGAAGGGGAAAAGAG | + | 7.95 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGCTGGGAA ATCCAAGGTT GGGGGGCTGC ATCTGGTGAG GACCTTCTTG CTGCATCATC 60
CTACCAGGGA AGGAGGAAGG GGAAAAGAGC AGGAAGGAGC AAGAGAGAAA GCAGGGCAGA 120
CTCACCCCTT TTATCAGAAA CCTGCTCCTT CAATAACTAA CTCCCATGAT AACATCATTA 180
ATCCATTAAT GAGGACAGGC CCAATAACCC TTAAATATCC ATCCTCTTAA CACTGTTGCA 240
TTGGAGATTA AGTTACCAAC ATTTGAACTC TGGGGGACAC ATTCAGACCA TAGCAGTCAG 300
TTATAAAAGT GTGATTTATG TTTTTTCCTA GTTTCATAAG CATAAGATGT GACATATTTT 360
AATAGTTGAC AATTCTACAG GGCCTGCTCT GAGTTCCTAG CCTAGATCAG CCTTTCTAGA 420
ACTTTGTAGA TTTTCAAAGA TGACCAGTGC TGCAAGCCAG GGTAATCTGG AATGTTCTGG 480
AAGCAAAGGA AGTGGATATG CCTTCAGCCA TAAGAATCAA AAAATATATG GTATTTAAAG 540
AAAAAGATTA TTCAGCTCAA ATCTTCCTAA AACATTTACA AAACAAATGT GCGTCAAGTT 600
ATAATACTGG GTGAAGTTAC CTCTGATTGG TGTTAACTAT GTTATGTGAG GATAACAATT 660
TCAAAGTATA TTAAAATGTA AAACTTGAAA ATGGTGGAGT CATCCTAAGT ATTATTTCAT 720
AAAATACCAG TAGAGAAGAA AAGGAGGATT TGACGTATAA AGATACGAGA GAAAAACATT 780
CAAAATTATG TGACCTCACA CAGGTAACCC TTTCAAGTGA CAGGGCACTT TTCAAGTGGA 840
AGCTTTCCTC CCTGCCTTGA AAACAAGGAT GTGTGACTGG TGTCCATTTG TATGTCTGTC 900
TGTCAGTCTG GAGTGTGTAG TCTCAGGAAG GCTGGAAGGT GATGCAAAAC ACTTTGATCA 960
TTTGTTCTTT GCGTTTGTGC TGCTATTAGC ACTTGCATAT GCTGTACTGA GACTTCTACT 1020
GACACGACCC CTCCAATCAA TGTATTTCTT GGAGGACTCC TTACTCACTT GTTCTAAACT 1080
TCAGTATCCT GGGTCTCTGA GTGGCTCTCT AGGGCAGTAA TGGTAGGAGG GCAGAGTTCA 1140
CAAACTATGT TCAATATTTG GAAAGGACTG ATTACCTACA GTAAAGTGAC TTGGCTGGTA 1200
AAATGTCAGG TTTCTTTGCT TTGGGTTGAT TTATAACAAC TCAATTTGGG AATACATACT 1260
ATCTCGATAG ATTGCTCTGA CTGGCATTTT TCTAGGTCTT TGATTTATAA ATGAAAGGGA 1320
GAACTGATTA TTCATTAAAT ACAGTCTATT TTTCCTAATT ATGTAGGAAA TCATATCTTT 1380
GTAATAAAAG GAGTGTTTGA TAGAATGAGC TCATGAAGAA GAGTGTAGTG TTCAACTGTA 1440
GTTCTTTCTA CTCCCCAGAT 1460
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