| Tag | Content |
|---|
EnhancerAtlas ID | HS095-31423 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr9:112204700-112206810 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HEY2 | MA0649.1 | chr9:112204978-112204988 | GACACGTGCC | + | 6.02 | | Npas2 | MA0626.1 | chr9:112204978-112204988 | GACACGTGCC | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_64489 | chr9:112204613-112206287 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I109442 | chr9 | 112204745 | 112206462 |
|
Enhancer Sequence | ACTTAAAACT GCTTGCCTGA TAAGCCATGA TTCTATTAGC ATGACAGTAA TGTGACTATT 60
TCTACTGAAG CCAGTTTGTA CTTTTTAGGT GCCCACAACT TCTTTAGCCC CCATTCTATC 120
AGTTCTTTGC AGAAGGGAAC CTGACTACTG AAGCCTGCGA TAGAATTCTT TATTTGCTTT 180
TTAAATTTTA CTCTAAATAG AATTTACTGT TTACAACAGG CAATTCCCTG ACAGCTTTCT 240
TCTGGGCAGA CATGAAAATA CAGTAAGAGC TAACACTTGA CACGTGCCAT GCACTATTCT 300
AATAGTTTTA CATACAGTCA CTCATTTCAT CTTCACTACA ACCCTTGAAG GAGACACTTA 360
TTATCCTCAT GGGTCAGGTA ATGAAACTGA GGTCTGGAGA AGCTCAAAGT CGGGCAGGTA 420
CAAGTGGAAA AGGCAAGACC TAGGTATATG GCTCCAGTCC AGTTCTCAAT GACTCAGCCA 480
GGGATGGTCC AACAATAAAG AATTTTTAGT TACAGATCAC CTTCACATTA TTGCTTAATT 540
TGAACCAAGG TAGCCATATT GAGAGCTGTC TTAAATCACT CACCTCAGTT TTACAGGTGA 600
GAAAACCAAG ATTAGGAGAG GCAATCCCAC ATAACTGGCC ACCGGAGACA TCAGATTTTT 660
TTTTTTTTTT TTTGAGACAG GGTATCACTC TGTCACAAAG GCTGGAGTGC AATGGCATGA 720
TTATGGCTCA CTGCAGCCTC AACCTCTGGG GCTCAACAGA TACTACCCCC TCAGTCTCCC 780
TAGTAGCTGG GACTACAGGC ACCGCACCAC CACACCCAGC TAATTTTTCT ATTTTTTGTA 840
GAGATGGGGC TTCATAGTGT TGCCCATGCC AGTCTCGACC TCCTGGGATC AAGTGATCCT 900
CCTGCCTCAG CCTTAGAAAG TACTAGGACT ACAGATGCAC ACCACCATGC CCAGATAATT 960
CTTCAGTTTT TGTAGAGACA GGGTCCTACT ATAATACCCA GGCTGGTCTC AGACTCTGGG 1020
GTTCAAGGGA TCCTCCCGTC TCAGCCTCCC AAAATACTGG GATTACATGC GTGAGCCACC 1080
ACACCTGGCC AGGGATGCCA GGATTTAAAT TGAATATGCC TATATTCTAG TTAGTGTTCC 1140
TGCCTCATAA ACCTGAAGCT CAGGCTGTGA ACACCAAACT TGCTCTGAGA CATGGGGAGG 1200
CTCAGTCTCC TCAGCTGATT GGCCTGGCAG ACACAGAGTT CACAAGGTCT ACAGATCATA 1260
AGAATACAAA CTGGTGACCA TGCCACTTCC CATATGGATG TGAAATGGCC GGGCCTGTCC 1320
CAGGTATATT GTAGGGAGAA GGGAAGGTTC AAATCCACCC AGGCCCATTC GCCTGTTTTG 1380
AGTTTCCCAC TAAGGAGGAG GCGATGCAGG TATCGATGGA GAGACTAACT CTGGTACTCG 1440
TCTTACTCGT GAATAGGGTC ATCTTTGATG TCCCCTGCCC TCCACCTCCT GGTTCCATGC 1500
AGGTGGGTGG GTAAGCTGCA GGCCCAGCCA CCTTGCTCTT CACCTCCTTC ATTTCTGTTC 1560
TTTCCTGGTA GGGAAATAGG CAGACCTAGG GCCACCTCAG GAGTCCGTCA GCCTTCTCTT 1620
GCTATTTTGC CTGTTCTGAG ACCAGAGCAG GGTGTGTAGT TCAGCCAGTG CCTGCTCTCA 1680
GACCTGATCA TCTTGCTGCC TTATCTATCT ATCACACAGT AGGTCAACAG GGTAATAGGC 1740
CAAGATGGTT TGGGCTTCTG GTAGAGGAGA TTTCTTAGGT CTGGAGCTGC AAATGGCTCT 1800
ACCTGAGTAC TATGCTGATG AACTGTACTG CCACCACAAA GCTAGCTACT ATAAAGTGAC 1860
ATTTTGCTCT CATCTGGCTA TACGTTCTTT TCATTGTGCC TACCCAGCAT CTACCCACAG 1920
GACTTGGAAG GGAATATACC CTCGATAAAG TTTTGCTGAT TGAATGAGCG GATTCCTACT 1980
CCAGTTTAAA CCAGCCTTCA AGAAAATTCC ATCTGGACTT TCTATCCAAT ATGGTAGCCA 2040
CTAGCGACGT GCGGTTAGTC CAAATTGAGA TGTACCGTCA GTGTAAAATC CAGACTGATT 2100
TTCAAAGACT 2110
|
