| Tag | Content |
|---|
EnhancerAtlas ID | HS108-33653 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr6:4370870-4373300 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HLF | MA0043.2 | chr6:4372458-4372470 | TGTTATGTAATG | - | 6.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_41322 | chr6:4368639-4372947 | Left_Ventricle |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I004368 | chr6 | 4369210 | 4372398 |
|
Enhancer Sequence | CCGGCTTTTT TGTGTGTGTT TTTAGTAGAG GTGGGGTTTC ACCATGTTGG CCAGGCTGCT 60
CTCGAACTCC TGACCTCAGG TGGTCTGTCC CCCTTGGCCT CCCAAAGTGC TGGCATTACA 120
GGCGTGAGCC ACCGTGCCTG GCCAGAAGAG GGAATTTATT ATGGGAATTG GCTCACATGA 180
TTATGGAGGC CCAGAAGTCC CACGATCTGC CAACTGCAAG CCAGAGAATC AAGGAAACTA 240
ATTCAGTCTG AGTCCCAAGA CCTGAGAACA AGGAGAGCTG ATGATGTAAC TCCTAGTCTG 300
AGGCTGAAGG CCTAAGAACC AGGAGCACCA GTGTCTGAAG GCAGGAAAAG GTGGGTGTCC 360
CAGCTCAAGC AGAGGGAGTG AAATTATCCT TCTCTTACCT TTTTGTTTTA TCTTGGTCCT 420
CAATGGATTG GGTGATGCCT GCCCACAGAG GGAAGGGTTA CCTCCTTTAC TCAATCCACT 480
GACCCCAAGG CCAATCTCTT CTGAAAACAC CCTCACAGGC ACACCCAGGA ATAATGCTTT 540
CCCAGCAATC TGAGTATCCC TTAGCCCAGC CAAGTTGACA CCTACAGTTA ACCATCAGCC 600
TGTGTCACTC CTCCACCCTC TTCCTTATAG ATCCCGCCTC ATCCCCTTCC CTTCCTGCAT 660
GTCCCGTCCA CCTCCTCTCC CCAGGCAGGA TGGAGACACC AAGAGACCTC CAGATCCCCA 720
TCGGGTAAAC CCACCGAGTT GGACTCTGAT AGTTGACTGT CACATAAGCA GACTGCCTGA 780
TGTACCATGC CCTGTTCTCT AAGCTCTCTG ACATATTTAG TGGGTGTTGA TGTCTCTGCT 840
TTGATGGAGA GGAAACTGAC CCCACTGTGA GTTGTTGGCT TGTCCAAGGT CACCCAGCAC 900
ATTAGCAGGA GTTCCAGAAT TGGAGCCCAA AGCTCCTGAG TCATGGCCAA GTGACGAGCT 960
CCATTGCACT ACGTGGCTCT TTGTGGCTAT AAAAAGATCC ATCTCTGGAG AGCACCTCCT 1020
CCAAGGCTTG CTGAGATAAG CTAGATGCTG GCCCTGTGTG TGTGCCTTAA CCGGGCAGTG 1080
AGCCACCAGT CCCCTGATAG GAAGAGTGAC TCTCGTGGGG AGAGGAAGAA AGAGAATGCT 1140
TCAAGAAGTC GGAGGAGGCA GCCTTTTACC TTAAATGGCC CATGCTCAGA TCAAGACACG 1200
GCACAATTAT TGTGTCTATA TTGTAGCCTG ATCTGCCACA AGTTGAGAAA AATCTCTTTT 1260
TCCATAGCAT AACTATTTAT GGCATTTGCC AATTTTCTCC GTGTAAACAC TTTTCCTGTG 1320
GCCTATTTCA AGGTACAAAC AGGAGGTCAC TGGACACAGA ATCTGGGGGA GATGTGCGCA 1380
ATAACAGCTC AGGAGCTGGT CTGAGCAGTC TCCAGCCCAC CACGTCCCTA ACCTTACTCA 1440
CCCCACCCCT GCCAATGTCC TCATCTTTAG GCAAGGATTA TCATACTAAT CAAGAGTTCT 1500
CCATCTAGAG TTTATCGTGT GTGATACCTA GCTCAGCGAA GTAAGATTCT GATGCCCTCG 1560
TGTATGAAAT GGGCTTGGAT ATTATCTTTG TTATGTAATG TCACGCCTAG AAATAAACAG 1620
GACCTGTCCT TACAGGCACT AAGTGTACCA TCACAACATC TGCTGCCCAG TTTTGAGATT 1680
AAGGGCATGA CCCTGCCTGG GTTCAAATCT TCTCTTTGAC ACTTAACTAG CTGTGTAATC 1740
TCAGGCATTT ACCTACCTTC TCTGTGACTT AATTTTCCCA TCTAACTAAT GGGAATACTG 1800
GTAATATGAA TCTCATAGGT AGTTATGAAG ATTAAATTAT TTAGAAGATG TCAAGCACTT 1860
AAAATAGTGC CTACTAGCAA TTGAGGGCAT AAGTGACCCC TAATAAATGT TAAATCACAT 1920
TATTACTACA TGCTGGCAGG TCAAAGGTGC ATCTGTTAAC AGATGGGGAA GGTGTGGCAG 1980
TGGTAAGCTT GCACTTGGGC CATGCACAGG TGTAGAGAGA ATCAGCAAAG AACATGTAGA 2040
AAGGTACTCT CATCTCAGAA AAAGGGTGTT GACAGCACTT AGTTCAAGCT TGCCCTTTTC 2100
CCAAAGGGCA AATCCCTTCC ACCGCATCTG TGCCTGCTTG AACAAGTGCA GTATGGGGAT 2160
CTCATTACTT CTCAAGGCTG TTTGGTCCAC TTTCAGACCT CTCTGATGTG TGCATCTCCT 2220
CACCGTCCCC CAATTCCAAA TCAGAATTAG CCTTCCAGCA GTGTAGAGCT CATTGGTCCT 2280
AGTTAGTCTT TCTGGAACCT CACAGAAAAG TTTGATTCCT CCTCCGCCTG AGGAGACATC 2340
ACAGAACTAT CATAGCTCTG AAAGCTGACC CCTTGGGAAA CTTGGTGCTC TGAGGATCTC 2400
AACACTCAAA GCCACAACAC AGGCCCTCAG 2430
|
