| Tag | Content |
|---|
EnhancerAtlas ID | HS043-26993 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr22:24487800-24489190 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr22:24488012-24488023 | TTCTTATCTCT | + | 6.32 | | Gata1 | MA0035.3 | chr22:24488012-24488023 | TTCTTATCTCT | + | 6.32 | | Gata4 | MA0482.1 | chr22:24488013-24488024 | TCTTATCTCTC | + | 6.32 |
|
| | 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 |
| GH22I024091 | chr22 | 24487437 | 24489361 |
|
Enhancer Sequence | ACACCATGCT GGCCCAGGGC GGGGAAGCAG GGCAGGGGCA GGCTGGTTTC TTTATCTCCC 60
TGGGCATGTG GCTCAAGGTT CCAGTGACCG TCCTTCAACC TGCCGCAAAC TTATCTGTGT 120
TGAGCAGCTT CATGTGCAAT TGAATTAAAA CATCATTTCC TCTCTTTTCC CAAGGGGTGT 180
TTATCATCCT TTCTGGGAGA GTGACCATTT TGTTCTTATC TCTCAGAAGA AAATTGTCTT 240
TCCTCACTAA CACAGGTTCT AAGAACCTGA CCTTGGTGAT GACAGTCAGT GCTACATAGC 300
ATCTCCCAGG CCCAGGACAT TCACACCCTG TAGCCTGGCA GGAGGGAGGG CAGGCACCAT 360
TGCCTCCAGG GTGCAAATGA GACATCCAAA GCCCAGCCTG TGCCCAGGCT ACCCAGGTTG 420
GCAGGGGCTG AGCTAGGGTG AGCAGCCTGC TCTCTTGACC CCCAGTTTGG AGTCTTCTGA 480
TTGTTGTTCA AGAAAAGAGC AGTTCTTTAC TCCCTGGATT TTCTCTCATG GTTTCCAGAG 540
TGTTTCTGAT GAATGCTGTC ACTGTTGCTT ATAGCAGTCT TGTGAGGCAG GCTGGGCAGC 600
CACGATTGTC AATTTTGTAG GCAGGAAAAC CAAGGACATT GGTAGAGATC CAGATGTCCA 660
TCATTTGGTT CAGCCCAGGA CTTGAAGCTT CTGAAGGCCC TGTGCACGTT GGCTTTGCCC 720
TTTCTGAGGC TATGTGCCCA GTCTCTACCA GTCTCACGTG CCCAGCAAGC CTCTTGGAGT 780
GTGGACAGAA TCTGCTGCTT GCTTTTTTCT GCCTTTGTGA TTTTTTTTCC TGATTATAAA 840
AGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTT TTAAAGAGAT 900
TCAAACAACT CAGAAGTGTA CAGTGTGAAT GTGAAGGCCC CTAGTGATTC CAGTATGCCC 960
CTCCATAATC CCTAAGAGTT TGCTATGTCC CTGTATGTCC GAATTTTTTC CTATTAACAT 1020
ATAAACATAT AGTAACATTT TCTTATGATT TTGCAGCTTG CCTTTTCGCT GGACAAAATT 1080
TAATGGAAGG TGTGGTGAGC TTCCCTGCCT GCCCTAGTGC CCTGTAGTTT AGCAGGGCGT 1140
TTGTTTATCT GCACGGACCC TTGATAGGTT TGGTTTCCTC TCCACTTCTT GCTATGACAA 1200
GGCACAGGCA GTGCATGTCT TTGTACTTGA AGCAGGGAGC ACATCATGAG TATTTCCAAG 1260
GACTAGAGTC CAAAGGTGGA ATTGCCAGGT TGTTTAGCAT TCTGATCAAC AATGGCTACT 1320
TGCCCCAAGG TCGTACTGAC TGATGAGAGT GTTTGCTTTC CCTCAGCCAT ATTGATGAGG 1380
TTCTCTTTTT 1390
|
