| Tag | Content |
|---|
EnhancerAtlas ID | HS118-16493 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr6:123118500-123121090 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr6:123120668-123120684 | CCCAAAGTAAATAAAT | + | 6.31 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_29458 | chr6:123118332-123121457 | Fetal_Intestine_Large | | SE_39152 | chr6:123120095-123123377 | IMR90 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I122797 | chr6 | 123118484 | 123121777 |
|
Enhancer Sequence | TAGACCTACA AGGATGTGCA TACCCTGATG TAAGCTAGAC TGTAAATAAA AACAAAAACT 60
TACAAATTGC CATAAGAAGC AAAGAGGAAG GAGGTCCATG TTCAAGTCAT AGTTTATCTA 120
ATTAAGACAT GATTCAAGGC AGAAACCATG TTCAGAGCAT TTAATGCCTG AGATACCCCC 180
GGCTCAACAG GTTTTTATTT GAGAACCAAC CTGTGCATAA CAGCAAGATG GCCGTCCGGT 240
TTACAGCATC CTATTGTAGT AGTGTAAAAT CTTAGATTTG TACCCAGAGA TTTTTGTTTA 300
AGTCCAGGGC TGGGCAATTG TCTCCTGTGG TACAAATTCA GCCTGTTGCT TGTTTTTGTA 360
AATAAAGTTT TATTGGAACA CAGCTATGTT TCCATTCATT CTACATTGCT TTTGATTGTT 420
TCATGTTTCA GAATAGAGCA GTTGAAATGG ATAGAAAAAG TTTGCTGACC CCTGGTCTAG 480
ACCTACCCTT CATTTTGTAG GTGAGAAAAT GAAGGCTCAG AAATGTGAAT TACTTGTCCA 540
AGTGCTCCAC ATCCCTTGGG AGCAGAGCCC ATACGCTAGA TCTTTTTACC TCAGATCTGT 600
GTTCGCTTAA ACCAACATCC TTTTGCACAT CCCTTGCCTT GCCTGATTAA CATACTCAAT 660
ATTTCCCAAA CATATCTACT TTCACGCCTC TCTGTGTCCA CATTTTTCTC TTTGCTTAGA 720
ATATCTTCCA TCTCATGTCA AATGAATGCT GAACGGGGGT TTTGATTATT TTTAGTTAAT 780
CGAACCTGAA TACAGTAATT TTGATGAGTT GTATTCTAGA ATAAGCTTAA GTTTCCAGTG 840
ACTTCTTGTC CCTGGCCTAC TATCTTGAGA TGAGTAATAT GTGAGTCCTT TTGAGTCAGC 900
CTGTCAACGA GCATTTGTTC CTGTTGATAT GTTAGACCAC ACAGTGAAGA GGCTTGGGAA 960
CAAATGAGCT CCAGCAGCCC AAGGTCACAC ACATTGTGTT TATATGCCTT AGGTGGCAGG 1020
AAGACTGGAA TATTGGAAAA CACAGGTGTT CATAGTCACT AGAATGTAAA TCTTTAACCA 1080
GCCCTGCTTT CCACTCCCTC CCTCTCCGCC ACCACACCTC CCTCCCAGCC CTGCTTTTAA 1140
TAGCTTGGCC AACTCGGGTG ATTCACTTAA CCTCGCTGAT GCAGAGATCA CTCATTTGTA 1200
CATAGAAGCT AGAAATACCT ACCTTGCAAA GCTTTTGTGA GCATTGGTGA TATGAAAAAG 1260
GCATAGCTTA CTATCTGGCA CAGCATCAGC CCTCAGTAAG TGGGCTGGTG GTGATTGTCA 1320
CATTAAGTGG TGACAGGGGA TACATGTTTG TAACTCCTTT GAGGATTTGT TTGATTTTAT 1380
TTTTATCTCT GTCCTCTTTT TGTCAAGTCA GATCTTACAA TTCAAAGACA GAAATGCTAC 1440
CTAACTTCTA TAACATATCC TATTATATTA ATATATACAG CTAGGGTAAA TTGGGCAGCC 1500
TACATACCTT TAACAGTTAA TTTTTTTTCT CTTTCTAGCT TATGATCTTA TATCTAAAAA 1560
TGTTCTTTCT GTTATTCTAC TACCATCTTT CCACCTCACA GTTTCGGAAA TGTCAAATGT 1620
AACATGAAAG CTCCACAACA AAATTTCTTA GAGGCTGATG TCTGAGATCT AACTCTGGAG 1680
AATGTTAGAA ACAAATAAAT TTCATAAGTG CTATTTTTCC ACTGAAATTC TATGTTCATG 1740
CAGCATAGCT ACATAAATAT ACATATACAG ATGCATGTCC CCACCCATGA CATCAGAAGT 1800
AGGTATCAGT GTGGACATCC TGGAGAATTC TTCCTGTTGC CACCCAAGGA AGGGTCCCCA 1860
TTTACTCCTA CACTGGCAAG ACTGGTGCCA CCGAATTTGT GGGTAGGTCA CTTTCCATTA 1920
GGCTTCATTT CTCAGCAGTG GTTATGTCAC AGCCAAAAAG GACTGGGAAG GAAACATGGT 1980
GCAATAGACA ATTGACTGTG AGAGTAATCA TGGGATTTAG ACCAGCCCTG AGACTGACAC 2040
CTATCCCTGG ATAAGCCATC TAACTTCTCT GGTGCTTGTG TTTCTCATGT TTAAAATAGA 2100
GAAGAAAGTC TAAGTGATTT TTACATAATT CTAAGCTTCT CCATCACCAC ACCATACTTG 2160
GCATCCATCC CAAAGTAAAT AAATGGCCAA GACTTTATGG CTTTTTATTA TATGATGATA 2220
ACGATGCGTA CCAATTTTCA ATCAGAATCT AGATTGGCCT AAGCTGTTGT GTAATTCTCA 2280
GACAGGCGAC CCTGATCTTG GACACAAACT GAAAATACAT GTTTAGTCCA ATTAAAACAA 2340
GTCATTTGGT TATTACTTGC CCTATATGTA TCTATATGTT CATCATGTAT TAGACGCATG 2400
TATCAAGAAC TACTAGGACT TGGGCATCTT CTTGAAAAAT AACTTTTGAT AAACTCCTCT 2460
CAGAAATAGG TCTATTTTAC CAATGTACAG AAGTAAATGA AGAGAGTGAA GAAGGGGTTT 2520
CAGTCATTTA ACATAATTTT TTAAAACAAA ATTAAAAACA ATTATCCAAT TCACAAATGA 2580
TTTATGGGTT 2590
|
