| Tag | Content |
|---|
EnhancerAtlas ID | HS073-02704 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr11:102469040-102471770 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr11:102471436-102471451 | TGAACTCCTGACCTC | - | 6.22 | | Sox6 | MA0515.1 | chr11:102469116-102469126 | AAAACAATGG | - | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I102597 | chr11 | 102468396 | 102472638 |
|
Enhancer Sequence | CAGCTGCAGG ATGTATTGGA ATGAAAATAA ACAGATTATA TCACTAGTCT ATAATTTGAT 60
CTTTGATAAG GAAGGCAAAA CAATGGAGTT TATTGATATT TTAGATCTGC TGATTAGATA 120
TTTAGCTGCA CTGTTTATCT TCATGTACCC ACTATCTTAT GCTATGCTGG CACATAGTCA 180
GGGTTCAATA CACATTTGTT GGCTAAATGA ACGGGTGCCA GAGAGATGAT TGGAACTTAC 240
CTGATCAACA AGTTTCATAT TCTTTAAAAT TTTCATTCAC TTTTACCAAA GAACAGTAAC 300
TAACTCATCA AATTTGAGAT TTGGTCTCTG ATAACTTTCA CCTGGCCTCT TGCAGCTCTT 360
TGCTAGTTCC TTGAATTCCT CCTCCAGCAT CATGTATTAT TCATCTTTTT ATCCTTGGGC 420
TTAGCATGCT GCCTGGTGCA TCCAGGGACT TGATGCATGT TGTTGAGCCT TAAAGGTCTT 480
CTTTTGTTTT ACCCAGTCAT CATTCTCCAC CTACCTAAGC TGACCCCATC AGACTTTCAT 540
TTTCAGGAGA TGCCTTCACC CTTTATTTGC TGGACAATCA AGGCAACTCA GCACAAGCTG 600
AATGAGTGGC CCAATTTTCA TCGTCTTTAG TCTCACACTC TCTTAGATTC TGATCTCTGT 660
CATCTTCTTT CCTATTTGTG GGAAGGGGTG TCTTTCTTCT ATCTTTTTTT TTTTTTTTTT 720
TGAGATGGAG TCTTGCTTTG GTGCCTAGGC TGGAGTGCAG CGGCGCAATC TCAGCTCACT 780
GCAACCTCTG CCTCCTGGGT TCAAACGATT CTCCTGCCTC AGCCTCCCAA GTAGCAGGGA 840
CTACAAGCAC GTGTCACCAC ACCTGCCCAG CTAATTTTTG TATTTTTTTC AGTAGAGATG 900
GGGTTTGACC ATGTTGGCCA GGCTGGTCTT GAATTCCTGA CCTCAAGTGA TCTGCCTGCC 960
TCGGCTTCCC AAAGTGCTGG GATTACAGGC ATGAGCCACC ATGCCGGCCT CTATCTTTTT 1020
GATTCTCTGT TTAATTACTG CTCACTCCCC TGAGATCAGG TGATGTGGTG CAGTGAACAG 1080
AACAAGAAAT GCTTGAAACC TTGTTTTATA ACTGGCTGTG TGACCTCGTG TGAGTCATTC 1140
AATTTTTCTG AGACTCAATT TCCTACTGTC AAATAAGAGT GAGAATAATA TCTGCACAAA 1200
CACTTAAAAG GATCAATTGA AATAATGCAT ATGAAAGTGT TTTATAAATT CAGGACTATT 1260
CTTATTTGTA GACACTTTAA AAAGACATGT TTTTACTCCA CAAATTTATT AATAGATGAT 1320
ATGCAGAATA TAAACTTAGA GTTTATCAAT ATAGCCAAGT TTCCTTCTTA GTTTGCTTCA 1380
CTGGAAACTT TGAAGTACAA ACTGTCATGT CATTGGCTGA GAAGCCATTC ATTCTATGGG 1440
ACTCATTAAC CAGGGCTGCT TAGTTCATGA TGAGTCAGAA GCCAAGAAAT CAACCATGAA 1500
TCATCCACCT CACTGAACCC AAGAAAAATA TAGTTCATAC AACTAAAAAC CCATCTGTAG 1560
CCAGTGCTGT GGATTAATGA TAGTCAAAGC TGTGCATAGT GCCCTTAAAT TAAGAATGTT 1620
TGTACCCATC TGAAGAGCCC GTGAAAATCC ATATTCATAA GCCATAACCT GTGAACATGT 1680
AAAGGGCCCC TCCTCTCTCA GAATCAGGTG GTTCAGAAGA AATGACAATG AGTCAGGGAT 1740
GTTACTTCAC CTCTGCTTCT TTATCTGAAT TCTTAATAGA TCACAGAGAA CCGCTCTAAG 1800
TAAACACAAT GCCATTTGTT GGCTTTCAGG GAAGTAATCT TACAGCCAGA AAAGACACAT 1860
TCCCAGGGAG AATGCGAAGG AGGAAGACTT CCTCCTGTTC CATGGTGGGC TTACCTCAAG 1920
CCCATGGCAT CCTGGGAATT CCCAATTTCA AATCTACTCT CCAGAAATAG TGGTTACTGT 1980
TATTGTTTTC CTTCCTGTAG CATCTTGTAT TTCTTTTTCT CCACTGTCTT CAAACATGAA 2040
CAGTTCCCTC TTTGAAATCC TGTCTTGGCC CTGCTGCCAC TGCCAACTAT TATCTTAACT 2100
TCTTTTGTTA TTAACAAGCT TCTCAAATGA ATGATCTATC TCAACTCTTT TGTTTCCCCC 2160
CATTTGCTTT TTATTATTTA TTTATTTATT TTAAGATAGG GTCTCGCTCT GTCACCCAGG 2220
CTGGAGTGCA GTGGTGCAAT CTCAGCTCAC TGCAACCTCT GCCTCCAGGG TTCAAGTGAT 2280
TCTCCCACCT CAGCCTCCTG AGAAGCTGGG ATTACAAGGC ACTGCCACCA CATCTGGCTA 2340
ATTTTTTTTG TATTTTTAGT AGAGACAGGG TTTCACCATG TTTCCCAGGC TGGTCTTGAA 2400
CTCCTGACCT CCAGTGATCC ACTCGCCGCC TCTCCCAAAG TGCTGGGATT ACAGGTGTGA 2460
GCCATTGCGC CTGGCCCCAT TTGCTCTTTA ACCCCTTTCC ATGATCTGGC TTTCTTCCTC 2520
ACTGCTCTGC TGTGACTATA TTCCAAACTA TCCTGGCCAC TCAGTCCCTT TTCTTCAGTC 2580
CTCAGTCTGG TGACCTTGGC AACATTTTCC ACTGTTGATC ACTTAAAAAA AATACACCCT 2640
TTTTTCCCAG ATTTATTTGG GATTTCACCA CAGGGGTTTT GTCTCTGATG TCAAACAGAA 2700
CTAAGTTATA ATTCCAGCTG AGGACAATGA 2730
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