| Tag | Content |
|---|
EnhancerAtlas ID | HS103-01626 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr1:171877950-171881180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:171878035-171878053 | CTGTCCCTCCCTCCTTCC | - | 6.16 | | EWSR1-FLI1 | MA0149.1 | chr1:171878103-171878121 | CTTTTCTTCCTCCCTCCC | - | 6.24 | | EWSR1-FLI1 | MA0149.1 | chr1:171878115-171878133 | CCTCCCTTTTTTCCTTCC | - | 6.53 | | EWSR1-FLI1 | MA0149.1 | chr1:171878052-171878070 | CCTACTTCCCTTCCTTCC | - | 7.07 | | EWSR1-FLI1 | MA0149.1 | chr1:171878043-171878061 | CCCTCCTTCCCTACTTCC | - | 7.38 | | EWSR1-FLI1 | MA0149.1 | chr1:171878064-171878082 | CCTTCCATCTTTCCTTCC | - | 7.69 | | EWSR1-FLI1 | MA0149.1 | chr1:171878060-171878078 | CCTTCCTTCCATCTTTCC | - | 7.91 | | HSF1 | MA0486.2 | chr1:171879431-171879444 | GAAAATTCCAGAA | - | 6.17 | | NFAT5 | MA0606.1 | chr1:171879427-171879437 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr1:171879427-171879437 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr1:171879427-171879437 | AATGGAAAAT | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr1:171878364-171878379 | GAGGTCAGGAGTTCA | + | 6.22 | | Nr5a2 | MA0505.1 | chr1:171878372-171878387 | GAGTTCAAGGCCAGC | + | 8.25 | | RARA | MA0729.1 | chr1:171878364-171878382 | GAGGTCAGGAGTTCAAGG | + | 6.73 | | REST | MA0138.2 | chr1:171880837-171880858 | TTCAGGACCAAGGACAGTAAT | + | 7.72 | | TCF3 | MA0522.2 | chr1:171878151-171878161 | AACACCTGCT | + | 6.02 | | ZNF263 | MA0528.1 | chr1:171878111-171878132 | CCTCCCTCCCTTTTTTCCTTC | - | 6.35 | | ZNF263 | MA0528.1 | chr1:171878064-171878085 | CCTTCCATCTTTCCTTCCTCC | - | 6.53 | | ZNF263 | MA0528.1 | chr1:171878095-171878116 | CCTCCTTCCTTTTCTTCCTCC | - | 7.36 | | ZNF263 | MA0528.1 | chr1:171878098-171878119 | CCTTCCTTTTCTTCCTCCCTC | - | 7.71 | | Zfx | MA0146.2 | chr1:171880666-171880680 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | 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 |
| GH01I171908 | chr1 | 171878039 | 171881229 |
|
Enhancer Sequence | TCTTAAAAGT AGGAGATATA TATTCCAAGC TTATCTTTTA CCATTGTCCT CTTACATGTA 60
ATGCTATAGC CATATTAAAT GTGGCCTGTC CCTCCCTCCT TCCCTACTTC CCTTCCTTCC 120
ATCTTTCCTT CCTCCTGCCT TTCTGCCTCC TTCCTTTTCT TCCTCCCTCC CTTTTTTCCT 180
TCCTTTTAAC TAATATTTTT GAACACCTGC TATGTGCCAT GTGTAGTAGT GGGAAGAAAA 240
TAAATGACAT AGTCTTTGCT GTCTCTGAAC TTAAACTGGA TACTAACAGT CCCAGTTATG 300
AAAGTGAAAA CAGAAAGCTT TAAGATTATT TAGAAAGTCA GAGGTGGTGG CTGGGCATTG 360
TGGCTCACGC CTGTAATGTC AGCACTTTGG GAGGCCGAGC TGGGTGGATC ACTTGAGGTC 420
AGGAGTTCAA GGCCAGCCTG GCCAACATAG CGTCTCTACT AAAAATACAA AAATTAGCCA 480
GGTGTGGTGC TGCATGCCTG TAATCCCAGC TACTTGGGAG GCTGAGGTGG GAGAATTGCT 540
TGAGTCTGGG AGGCAGAGGT TTCAGTGAGC CGCGCCGAGA TTGTGCCACT GCACTCCAGC 600
CTGGGCAACA GAGTGAGACT CTGTCTTAAA AAAAAAAAAA AAAAAGTCAG AGGTGGAATC 660
AGATTCTGTG AAGAATTAGA AGAGGCATCA GAAGACACTC TTTAGTCTTC GTATTTTAAA 720
GATGTAGAAA CTGAGTCTCT TATAGATTAA ATGATGTGGT GAGGTTACAG CTGAAACCCA 780
AGCTGGTTTC TTGACTAGTG CTCTTTCCAT ACCACCTCTT CTCTCTTGAC TATCACATTG 840
CCTGCCCAGA TCCCATGTTG TCATATATTT TTGTATGTAG TTTGTGCTGT CAAAGACCTC 900
TTTTCAAAAT GCACACACTC AACCATAGAC TGTTACCGTT ATTGGTTTTG TTACTTGAAA 960
TTATAATTGG AACAATTAGA GATGCGTCAG TGGAAAGGCA ATGAAAGAAG GCCATTAAGT 1020
GCTAATAAAT GCCTCTCCTC ATGGGAACGG AGATCTTTTC TTCTCTATGT ATTTGAGCTC 1080
TTTTCACTGG TGCTTTTAAG TGGCTAGAAA TAACACTTGC CACACGCTTG TGGAATACTC 1140
TGGATGCCAG GGGGTTCATT TTATTCTGTA TTTGAATTGA GCACACTGCG GTTGGAATGT 1200
GTGTTGATTC TTTTGTTGAT TTAAGCATTC ATTCCATGTT TTGCATTAAC CTTTTCTCAT 1260
GGAAGACAGA ATAGTGAGAG CTCTTAGAGA ATGAAGTCTT TAGGTAGCTG ATGACTTTCC 1320
AAGAAACAGA TGAAAAGGTT AAAGTTGTAA GTGTTTATGT TGATATATTT TCCTTTTCAT 1380
AACACCCTAA AATCTAGATA CAATAGTCTT CCCTTATCTG AAGTTTTGCA CTCTGCTGTT 1440
TCAGTTACCC ATGGTCAATT GCGGTCTGAA AAGACTCAAT GGAAAATTCC AGAAATACAC 1500
AATTTATGTT TTAAATTGCA TGTCATTCTG AGTAGTTAGT TAAATCTCTT ACCATTCTGC 1560
TTTGTCCCAC ATGGAATGTA AATTATCTCT TTGTCTAGCA TATCCACATG GTATACACTA 1620
TCTGCCTGTT AGTATTATAG AGTCAGGTAC TATCTGTGGT TTCAGGCATC CACTGGGGGT 1680
CTTGGGACAT ATCCCCTGCA GGTAAGGGGG AGCTACTGAA CAGTGTGACA AATTGGATGT 1740
AGCCCTCCCT AAAGCTACAT GCTTACCTGT GGCTAGCAAG AGATAATCAC TACTTGTTGA 1800
TATGGTGATA TATTAGCTTC AGAAACGAAT TTAGGTAAAT AATGAATGAA TTCCAGAATA 1860
ACTTACCAAT ACTAAAAATG ATGACAATGA TAGTAATGAT GATGATAAGG ATAATAGCAG 1920
CTAATATATT TGACTACTTA CTATGAGCCT GTAAGTCTGT GCCTTATAGA AATGAGCAAG 1980
GTTGTCCTGT CCTAAGAGAG GCTACATAGG AGAGGATTTG ACTTGGGCTC CTGGTACTTT 2040
TGGAAAAAAC AGGAGGGGCA TCTAAATATG CCGGCATATC AGGAAATGCT TCCCACAGGA 2100
GGCTGCATCA ACATGTCTTT AAGAGTGAGT TCATTCCTCA ATAAAGAAAG AGGCATTAGA 2160
CAAAGGCTTC TGTGGTTAAG GAGTCAACAC TGAAGTGTGA AATTAGTGTA GAATCCCTTG 2220
GGAGCCAGCT GTTCTGGGAA TAAAAAGTTT GCGTGGGGGA ATCATGGATG TGGCTTCTAG 2280
AGAGTGAGAG AGAAGCTGGA TCCAGGAATC CACTTAAATC CTTCCTGGTT AATTGGAAAA 2340
TCAGATTCCA TTCTTTTTAA ATAAACAGGA TGTGACCATG GTAGTGCTCC ATTCTGTTTT 2400
AGTGGAGAAA GCAACCTACA CTTTTTTGGC TTCCAATTAA ATACCTCACT TTACCCCAAC 2460
ATCTTTTTTT TTTTTTTTTT TTTTTTTGAT AAAGAGTTTC ACTCTTGTCA CCCAGGCTGG 2520
AGTGCAGTGG TGCAATCTCG GCTCACTGCA ACCTCCACCT CCCGGGTTCA AGTGATTCTC 2580
CTGCCTCAGC CTCCTGAATA GCTGGGATAT TACAAGTGCG TGACACCACG CCCGGCTAAT 2640
TTTTGTATTT TTAGTATAGA CGGGGTTTCG CCATTTTGGC CAAGCTGGTC TCGAACTCCC 2700
AACCTCAGGT GATCCGCCCG CCTCGGCCTC CCGAAGTGCT GGGATTACAG GTGTGAGCCA 2760
CTGTGCCTGG CCTCTAGCAT CTTAAAATAG TGAAAACAAA AGAGTACACT ATTGGCTGGA 2820
GAAGCTCACT TCTACCCTAT CCACGCTCTT CTTTTCCAGC CTCCTGCCAA GGAGCTGGTA 2880
ATGTATATTC AGGACCAAGG ACAGTAATTG GGCCCCATTT CTTCATCTGA AGCCTTAGCA 2940
GGGGAGGGGT TGACGTGAGC TGTCTAGACC AGAACTGCCC TGGTCAGCGG GTAAGTGTTC 3000
TCTTGCTGTT GCTTCTTCTC ACTGGCTGGT TTGTCTTCCA CAGGTGGAAG ACAAACTTTT 3060
CTAGTCACTG TCGTGTCAAA GAAAAGTCTG AGATTCATGT ATGGGCTTCG TGGAGAGGGG 3120
CAAGGGAGGC CTTTGAGCCT CTTTGGTACC AGGCCTTAGG GCTACCTCTT ACCTAGGCCA 3180
AATGAGGATT TCATGTGGTC CAGCCCATGT TTCCAGGATT GGAAAGGGAA 3230
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