| Tag | Content |
|---|
EnhancerAtlas ID | HS180-05042 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:236325820-236327930 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPIC | MA0687.1 | chr1:236326962-236326976 | TTCTTCCTCATTTT | - | 6.42 | | ZNF263 | MA0528.1 | chr1:236327236-236327257 | CTCCCATCTCCTCCCACCTCC | - | 6.24 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_59322 | chr1:236304325-236328173 | Ly3 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I236162 | chr1 | 236326267 | 236327471 |
|
Enhancer Sequence | ATGGCAGCCC TTCCCATCAT AAGCCTTAAG TCCCTTTTGT GGGCTGGGCC CAGGGTCCCC 60
ATGCTGTGTG CAGCCTAGGG ACTTCGTGCC CTGTGTCCCA GCTGCTCCAG CCATGGCTGA 120
AAGGGGCCAA CGTAGAGCTC GGGCTGTGGC TTCAGAGGGT GGAAGCCCCA AGCCTTGGCA 180
GCTTCCATGT GTTATTGAGC CTGCAGGTGC ACAGAAGTCA AGGTCTGAGG TTTGGGAACC 240
TCCGCCTAGA TTCCAGAAGA TGTATGGAAA TGCCTGGATG CCCAGGCAAA AGTTTGCTGT 300
GGGGGTGGGG CCCTCATGGA GAAGCTCTGC TAGGGCAGTG CAGAAGGGAA ATGTGGGGTC 360
GGAGCCCCCA CACAGAGTCC CTACTGGGGC ACTGTCTAGC GGAGCTGTGA GAAGAGGGCC 420
ACTGTCCTCC AGACCTCAGA ATGGTATATC CACCGACAGC TTGCACTGCG CTCCTGGAAA 480
AGCCACAGAC ACTCAACACC AGCCCGTGAA AGCAGCCGGG AGAGAGGCTG TACCCTGCAA 540
AGCCACAGGG GTGGAGCTGC CCAAGACCAT GGGAACCCAC CTCTTGCATC ACTGTGACCT 600
GGATGTGAGA CTTGGAGTCA AAGGAGATCA TATTGGAGCT TTAAACTTTG ACTGACCTGC 660
TGGATTTCAG ACTTGCATGG GCCCTGTAAC CACTTTGTTT TGGCCACTTT CTCCCACTTG 720
GAACGGCTGT ATTTACCCAA TGCCTGTATC TCCATTGTAT CTAGGAAGTA ACTAGCTTGC 780
TTTCGATTTT ACAGGCTCAT AGGCAGAAGG GACTTGCCTT ATCACAGATG AAACTTTGGA 840
CTGTGGACTT TTGGGTTAAT GCTGAAATGA GTTAAGACTT TTGGGGACTG TTGGGAAGGC 900
ATGATTGGTT TTGAAATGTG AGGACGTGAG ATTAGGAGGG GCCAGGGATG GAATGATATG 960
GTTTGGCTGT GTCCCCCTCC AAATCTCAAC TTGAATTGTA TCTCCCGGAA TTCCCATGTG 1020
TTGTGGGAGG GACCTGGGAG GAAGTAATTG AATCACGGGG GCCGGTCTTT CTTGTACTAT 1080
TCTTGTGATA GTGAATAAGT CTCAGGAGAT CTGATGGGTT TATCAGGGGT TTCCGCTTTT 1140
GCTTCTTCCT CATTTTTTTC TCTTGCTGCT GCCATGTAAG AAGTGCCTTT CGCCACCCAC 1200
TGTGATTCTG AGGCTTCCCC AGCCATGTGG AACTGTAAGT CCAATTAAAC TTCTTTTTCT 1260
TCCCAGTCTC AGATATGTCT TCATCAGCAG CATGAAAACA GACTAATATA CCTCCTCATA 1320
CCTCCCATGC CTCCACACTT TTCACACTTC CTCACACCTC CCATACTGCC TCACACTTCC 1380
CACACCTCCC ATACCTCGAC ACACTTTTCA CATCTCCTCC CATCTCCTCC CACCTCCCAC 1440
ACCTCCCCAT GCTTTCAACA CCTCTCATAC CTCCTCACAC CTCCCATGCC TCCTCACACT 1500
TTTCAGCACC TCCTCACAGC CCCCATGCCT CTCCACACCT CCCCATGCCT CCCCACACCT 1560
CTCACACTTC CTACACCTCC TCACACCACT GGTGCTTATT ACTGACATGT CTGTCTGCCT 1620
GTGTATTTCT CTGGGACAGG CCCAGCTTCT CCTCCTTTTT ACAATTCTTG GGTCCAACCC 1680
AGGGTCTGAT GCAGACTCAG TGCTGAGTAT CAGTTGACCT GACTTGAACA CCACCAATTG 1740
GAAAGCCAGG ATGATGTAAA TTTTCATCTG GCCTCATTTG TTCCTTAGCC TCTCATAGGG 1800
GTCACACCTC CCTCTTTTTC ATTCTTGTAC ATCTGGGGAC ACTGAGCAGG AGGTGCCCGT 1860
GCTGTCAAAG CACCAGAGAG TATGACAGCA GAATTCACGT CTGCCTCCCC ACAGGAGCCG 1920
TCGCCCCTCC CAGCTGAGTT CCTGCCAAGG TCAGTGGGAG CCAGTGCAGA CTGGCAGAAA 1980
TGGGCAGCCG GATATGAGAG CCCAGCCGGC CAGAGAGCCA GGGTGAGCCA GGAGCTTTAG 2040
CTCAAGTTCC GGACACCCAC CAGTCTTTAG CAAAGTCTCT CAGAACACAG AGGGGAGTGG 2100
GTGGGAGAGT 2110
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