| Tag | Content |
|---|
EnhancerAtlas ID | HS092-10573 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr11:117253660-117255940 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I117383 | chr11 | 117254381 | 117255751 |
|
Enhancer Sequence | AAGGGCCAGT TTTGTGTGTC TGTCCCTGAC CTCCACTGCG TGTGGGCTGC TTCAGTGCCT 60
ATTCACTCTT GGGTGGTGGG AGGTGGGGCT CAGGCTCTGG CCAAGGGTTA GAGTGTAGGG 120
AGATTAAGCA TATCCTTGGT GCTCTGTGTG CAGCCTTGAG AGCCCCACAC AGGCATGACT 180
GATCCTTACC TGGGGTTAGC TTTGGTCTCT GGGGCTCCTG GTCAGGACTT GAGGTACAAG 240
GGCAGATGAG GGGGTACCTC CTGGCTCATT TGCTAAACTT GCTAAATCAT GTTTCCTGTC 300
TACCAAGCAC TGTTTTTCTC TTCAAAAATG TTGTTGAGGT ATGTATGTAC ACTGCAGTAC 360
ATAGGCCTAA AGTGTACAGT TCAGTGAAAG TTTGCATCTG TGCACACTGT ATAATGGCCA 420
CTCAAACAGG GAATGTCTCC ATCCCTCGAG GAAGTTTCCT CGTGCCCCTC TCAAACCACT 480
CACCCCAGAT CTTCACTGTT CTGGCCTGTG AGCTCCAAGT TCTGGCCAAA GGGTCATTTT 540
TCCAGTTCTC TACTTCACAT ACATGGAATT ATACAGTATA CAGGATTGAT CTTTTGTGCT 600
TGTGTTCAAA GCTCAGTGTG TTTTTCTGAT TCACCTATGT TGTTGAACCA AGTACTTCTA 660
AAATTTAGAA ATCATTTAGC TTTTCTCCTT CCATTCTTAC CCTTCCCCTT CCTACTCAGT 720
TTTCAGACGA GGAAACTGAG GCTCAGAGAA GTGAAGGGAT TCATCTAAGG TAACATCGCT 780
AGTCAGTGGC AGAATTAGAA CTAGATTATA GGCCGGGCGC GGTGGCTCAC ACCTGTAATC 840
CCAGCACTCT GGGAGGCCGA GGCAGGTGGA TCACCTGAGG TCAGGAGTTT GAGACCAGCT 900
GGCCAACATG GCGAAACCCC GTCTCTACTA AAAATACAAA AATTAGCTGG GCGTGGTGGC 960
AGGTGCCTAT AATCCCAGCT ACTTGGAAGA CAGAGGCAGG AGAATTGCTT GAACCTGGGA 1020
GGTGGAGGTT GCAGTGAGCC GAGATCGTGC CACTGTATTC CAGCCTGGGC AACAAGAGCG 1080
AAACTCTGTC TCAAATAAAA ACACTAGTTT ATAGTCACTA GAGCCCTAGA CTTCTGACTT 1140
TAGTCTGCAG CCACTGTTCC TTTTCTCTGC ATAGAGAAAG AGAAGGATCA GGACTTAACA 1200
TTTTCCCTTC TGTGAACTGA GCAGGTCTAA AGGATTTGGG ACTGACTCAT GAGCAGAGAC 1260
AGGTTTATGC ACACATTACT CACAGCAAGT TCATGCACAC ATTACTCACT GAGAGCTGGC 1320
AGGGCACGTG AGCTCAGGAT CTCATGTTGT CACCATAACA TTGCAGGAGT GGTGTATGGA 1380
AGGGGTGGTC ATGTCTTTCA GATGGTGATA CATCCTACAG TGAAAACTGT GACCTGGAGG 1440
AATTATATGG CTTTCCTGTC ACCTTGGTGG CTGTGGTTAG CCAGTTCAGG ATGCTTTCTG 1500
TGAGGACAGG AGGTGGATGT AGTTCAGAGA GAGGAAGATT GGGCAGAGGT CAGAGGGATG 1560
TCTTCCCAGG ACCTCTAGAG GGAAGCCTGG GCAGCCGGGC TCAGTTGGGG CCTTGGCTTC 1620
CCCAGCTCCT CCCCAGTTGC CTTGGCCGAT TCATTCCTTT GTCTTGTGTT TCTCCCGCCA 1680
TCCCAGCGAG GCTGCCCCTG CTAGGGTCTG AGAAATACCT GACCACGCAG TTTCAGTTTA 1740
TACCATCCCC TTAGGAAATG CCTTCTCTTC CTTTCCTGAG TCTCTTCAGG CCCCATCGCT 1800
TCCGTGTTAT TAATCTTTAC AGCGGCATCA GGAATGGATG GGTTGTCTAG GTTTTGTGGG 1860
AGTAGCTCTG TGTCTGTCAG CTTCCAAAGG TGTAGTCAAG CTGGATCTGA AGGGTTAGGA 1920
GCAGAGGGCA AGCTAGAGGG AGCAGGTAGG TCCAGGAGGC AACATGTGCC ACTCACCGAA 1980
TGCTTTCTGG CCAAGGCCAG GGCTAGGAAA CAGGAAGGTC CTCCCCGTGT CATGCCAGCA 2040
TCTTTCGTGA GGATTTCCAG AGAAGAGGGT AAAAGAATCC AAACCACCAA GTTGAGTATG 2100
AGAGGAGACA TAACTTTTGT GGTAGTACCA TGAAAACCAT TTCACAGTGT TTCTAGGTGC 2160
CATTTCCCCG CCCTCCGCTC TCTTTCTTCC CTGTCTCTCC CTGCTTTCCC TTCTTGCTTT 2220
CTCTCCCGTA TCTTTGAGCT ACTTGGTGGC CAGCCTGAAA TGATTATGCT CCTGCAGAGC 2280
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