| Tag | Content |
|---|
EnhancerAtlas ID | HS076-32937 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr2:113755420-113757630 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr2:113756570-113756580 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr2:113756570-113756580 | GGCACGTGCC | - | 6.02 | | ZNF263 | MA0528.1 | chr2:113756745-113756766 | GAAGGAGGAGTGGGTAGGAAG | + | 6.44 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTGGGACCTT GCTCTGACAT TGCCTTGGAT TGGAATCCAA GTCTATGGAG AGGGACTATG 60
TGTTTTCGTT CTTCGTGGGT CCATGTCTTT AAATTTTAAT ATAGTATTTT TACACTTAAA 120
ATGGTCATAA AGGATTTTAT TTTACTTTTT CCTTCTGTAA GATTTAGATA AAAGACTTTC 180
TGGCTTTCTC ATATAACTGG CTTTATTTTT TCATCTTTAT TACTGATGTC TGATTTATTT 240
CTGCCTTTTA AATATTTATT ATTTTAGCTT ATTTTGTTTT ATTTAGATTT ACATATGGCT 300
TTTAAAAAAG GTTCTCTAAG AATTTAATGA AGTAATGAGA TTAAACACTC AATAAAGAAT 360
AGAAATAAAC TCAAATAAAT ATGGAGGTAA ATATCAAAAA CAGTTAAAAG ACAATAAACA 420
AGAATACTTA TTGTTGTATT GTCCTGATCA TCTCCAGGAA ATCCAGGAAG TTGCTTTATA 480
ATCCATTTTC TTTCTATGGT GTAAAAGAAA TACTGAGTAG GTAAGAAGGA ATATTTGTAA 540
CAAATATATC TAAGGTCTAA ACAAAAGAGA CCTATATAAA CTCACCCAGA TGAATAAACA 600
GAACTAGGAA CTTTGGAAGA ACTGTATGCC CATCCTCTAT TCTATCCTCT TCTCTTCCTC 660
CCCACAGATG TAATTGTCAT CCTAAATTTG ATGGTAACTA TTCTCTTAAA TTTTGTTATA 720
GTTTTACCAT CTATGTATAT GCCCCTAAAA TAGATATTGT TTATGCTTTA AACTTTATAT 780
AAATGAAATA ATACTGTATG TATTCTTTTA CATCTTGCTT ATTCACATTC TTGGGATTCA 840
TGGTGATATG TCATGTCAGT TTGGGTGCTT TGATGAGAAG ATGTTAAGAG ATTTAATGGG 900
AGACATGCCT GAAGGCCAAA AAAGAGGGAT CAGGAGTAGG TAGGGAGAGC ATTCAGACTG 960
TGAGGCAGGA CTGACACCAA TGATAGAAAA GAGAGAAGGA AAGGCCAGGT GCGGTGGCTC 1020
ACACCTATAA TCTCAGCACT TTGGGAGGCC AAGGCAGGCA GATCACTTGA GGTCAGGAGT 1080
TCGAGACCAG CCTGGCCAAC ACAGTGAAAC CCCACCTCTA CTAAAAATAC AAAAATTAGC 1140
CAGCCATGGT GGCACGTGCC TATAGTCCCA GCTACTTGGG AGTCTGAGGA AGGAGAATCA 1200
CTGGAACCCA GGTGGAAGAG GCTGCAGTGA GCCGAGATCA TGCTACTGCA CTCCAGCCTG 1260
GGCAACAGAG CATCTTGAGA CTCTGTCAAA AAAAAAAAAA AAAAAGAGAG AGAGAGAGAG 1320
AGAAGGAAGG AGGAGTGGGT AGGAAGAGCG TCAGACTGCA GTGCACCTGT GAAGCTCTGA 1380
GAAAGTCTCA ACCTGGCACA TTGGGGAGCC CTAGAGCAAA ACTTGGCTGC AGAGGCATTC 1440
CACATCAGTA GGAAAGACTG CCATCACTGG CTGGGAGCAG CCCAAGAAAA GAGTGTTCTT 1500
GGCAGGAGCA CTGCCATGAA TCCAAAATTG CAGCAGCTGA GGTTGTCTTC CAACTGTTCT 1560
CCTTGTAACA GGTTCTTTTA AAGGGAAGTC TGAGAGTCAC ACCTCCATGC TCACAATCCA 1620
CTCTTGTGCT GCATGGACCC CATCCTCTAC GTATGTTTGG GAGCAGATCA TCCATGCCTC 1680
CCATGGGTGT CTACCTGAAG GGAAACTTAG CAGAGGAATG TTAGTGAATG GACTACAGCA 1740
CCCATTTCTA TAGTTGGGCC AACAGTTTGT TCTCATCATC TTTTTTCTCC GCTGTCTATT 1800
CTAAATTTCC TTTACCCTCA ACTAATAGCT TGGCAGGTCT TAGTGGCTTT CCTGGGGATG 1860
TGATCAAATC CCTCACTCTG GCAGTCATGT ACTTCTTGAG CTGGGGTTAC TGCATGTCTA 1920
TTCACATTTA GTTATTCAAG GGAATACCAA GAGGTGTCCA AATGGATCAC TTGGGTTCCA 1980
CAAATATTAC ACACATATAC CTCCCTATCT TCATATGTAA AAGCAGCTAT ACCTCCTCTT 2040
ACATATACTG CTGGATGGCA GCCCATCCTT CCAAAGTATT ACCACTTACA TGGTGTTCCA 2100
GGTATACCTC CAGGAGGCCA TTCAATGCTC CAACAGGTTG CTACTTTTGG GTTGACCAAT 2160
GAGTCCAGGG AAGTAGTGGA GCAGGCTTAT ACTGACTTTG CAGGGTCAAT 2210
|
