| Tag | Content |
|---|
EnhancerAtlas ID | HS108-34102 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr6:25981130-25983390 |
Target genes | | Number: 18 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr6:25981975-25981990 | TTAGCTGAGTCATTT | - | 6.35 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28528 | chr6:25980819-25982238 | Fetal_Intestine | | SE_29180 | chr6:25980781-25983387 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I025980 | chr6 | 25980909 | 25982829 |
|
Enhancer Sequence | CCACCCCGTA AACATTTTAA TTTCTCAACA TGGGTTTTCC TGGGTCATTC AGGTAATATG 60
AATTGAAACC CCAAACTTCT GTGAGTCAGG CTGATAAAAG CTAACTGAAT AGAGTTTGAA 120
AAAGGAGGGT ATTTACAAAG GTGAGGAGTT GGGAAATCCA CAAGGAACAG GAAGCACCCA 180
GAACTAGGAA CAGTTAGAGA GCCATCACCT CCTCTGGGCC TCAAGTGGCA GGTGTAGGGA 240
GCTGTAACTA TACTAGAGTG TGCCCAGAGG CAGAGGAATG CAGACCCTCC AAATCATAGC 300
GTGGGACTGG GGTACTGAAT ACTCCCAAGG CTGCTTCTTT GTGCCCTATG GTCTCCTCTG 360
GTGCTTCCCA TTGGCTGAAC CAAGCCAGAG GGCGGAAAGC CTGGTTAATC TGTCCATGTC 420
AGCCTTCCTG GGCACAGAGC AAGACAGGGA AAAGTGAGGG ATTATTTGGA AGAACAAACA 480
GAGAGCATCC AGCACAGGAA GTGTTTCTGA ATACTTGAAT TCCTTAATTG TCACAGACCA 540
ACTGATCAAC ATTTAACTCA GTAGCACAGT GGTTTCTTAA CTCTCTTGTT AGAACATCCT 600
ATTACCATTT TTTATTTTTA AAACTGCATA CTGTTCAGTA TCTCACTTTA GGTTATCAGA 660
TCTTTTTTCT GTCTTGTTTG ATTCTAGTCT GATATTTTTC ATGTATATTG GTCCTCAGTG 720
TATTATTATC TCATACTAAT GCTTATGGAA CATTATCTGA GGGGAAAGAG AAGAGCTTAC 780
AATTAAAAGT CATGGGACTA GGCATGTGTC ATGAGACCTG GGTCTTCCAA TAACAAGCTA 840
AGACATTAGC TGAGTCATTT TCCCTCTCTG ATTCTCAATG TTGGTGGTTA TTCAGTAGAG 900
AAGGGAAAAG GTATCTTTCT GCTCAACTGT CTCATGATTC CTGGAAGTCC TGCATGGGAG 960
AAGAACTTTG GACAGGATGG TAACCATATT AACAGGTTAG TTCTGTACCT TGGCATCCTT 1020
GAATAATTAA GACGAAGATG ATGTTGATGA TATCATTATT ACTACATGTT GTTAGAAGAG 1080
CTGAAGCAGG ACTGGCTTGT CTGTCATAAT GTAAAAGAGT CTTGGAAGAT GTCCGGGGTC 1140
CAGGGTCCAA AACCCCTCGT GGCCTTTGGA ACACCAAGCT CTGTGCCAAA TGGTGGAAGG 1200
CTGCCCTGCC GCACCACAAA TCTAAGCCTA GGGCATAAAA CCCCTTGTGG CTTGGATGGA 1260
ACCCAGGGCT CAGGGCATAA AACCCCTCAT AGCCTCTGGA AAGTGCACAG ACTTGTTGGT 1320
TCCTTGCTTT TCACTCATAA ACGTGTCCTC TACTATCTCA AGCAGCAGAG TATATTCTAC 1380
ATGTGTCAAA GAAAATGCTA AACTGTCACA GCTACGCTTA ATGCACCACT ACCTTTCTAC 1440
CCCCATGTCC TCATGCCCTC ACCTGTTTAC CCTCACGTCC TCACCACCTG CTTCTTTGTT 1500
TGATCACCAA TAAATAGTGT GGGCTCCCAG AGCTTAGGGC CTTTGCAGCC TCCAATCTAG 1560
TGCTGGCACC CTGGACCCAC TTTATGCACT CTTAACTTGT CTTTTCTCAT TCCTTTGACC 1620
CCGCCGGACT TTGTAGCCCC CACGGCCTGG TGTTGGGCCT GATCACCCCA ACAACTACCA 1680
CTTATTAGGT GGTTACCATG TACCAGGAAT TTTACCAAGC ATTAAGCAAA CATAAGCTTA 1740
TTCAATCCTA CCCACCATTC TCTGCAACAA ATACGGTAAT TTCCACTTTA TAGTTAACAA 1800
ACTGAGGCTC AGAAAGTTAA ATGATTTGCC TAAGCTCACC CAGTTTATAA GAAACAATAG 1860
TTGGGTTTGA ACACAGGCTG GTTTTATTGA AAATAACTTG TGGCTGGGCA TGGTGGCTCA 1920
CACCTGTGTA ATCCAGCACT TTGGGAGGCC GAGGTGGGTG GAACACTTCA GGTCAGGAGT 1980
TTGAGACCAG CCTGGCCAAC ATGGCGAAAC CCCATCTCTA CAGAAAATTT AAAAAAATTA 2040
GCCACTTGTG GTGGTGCGCA CCTGTAGTCG CAGTTACTCC GGAGGCTGAG GCAGGAGAAT 2100
TGCCTGAATC CAGGAGGTGG AGGTTGCAGT GAGTTGAGAT AGTGCCAGTG CACTCCAGCC 2160
TGGGTGACAG CAACACTCCA TCTCAAAATA AAATAAAATA AAATAACCTG TGTTCTTCAC 2220
AGCAACAAAA TTATTTTTGT TTGTTTTGTT TTGTTTTGCA 2260
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