EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

EnhancerAtlas 2.0

Tag

Content

EnhancerAtlas ID

HS091-26884

Organism

Homo sapiens

Tissue/cell

HepG2

Coordinate

chr2:97268600-97269980

Target genes

Number: 15
Name	Ensembl ID

AC012307.3	ENSG00000204685
STARD7	ENSG00000084090
TMEM127	ENSG00000135956
CIAO1	ENSG00000144021
SNRNP200	ENSG00000144028
NCAPH	ENSG00000121152
RP11	ENSG00000235480
ARID5A	ENSG00000196843
FER1L5	ENSG00000249715
KANSL3	ENSG00000114982
LMAN2L	ENSG00000114988
CNNM4	ENSG00000158158
CNNM3	ENSG00000168763
ANKRD39	ENSG00000213337
SEMA4C	ENSG00000168758

TF binding sites/motifs

Number: 1

JASPAR ID

Coordinate

Motif Sequence

Strand

-Log10(p-value)

IRF9

MA0653.1

chr2:97269043-97269058

AGTTTCGCTCTCGTT

6.17

GeneHancer

Number: 1
ID	Chromosome	Start	End

GH02I096600

chr2

97266508

97268845

Enhancer Sequence

TAAGAGAGGA CATAGCAGGA ATCAGTAGAG ACTCAATCAC TTGCACTATC CCGAGAGCAG 60
CCACATCCAT CCACCCTCAC CACCAACTAA AACACCAGTG GTGCTTGCCC TTGGACACCC 120
GTCCTCAGAG AGAAGGCAGG AAGCTCTCCC CAACTAGGCA CACACGCAAT GGATGCCACA 180
CAGGAAAGGT ACTGTGCCAG ACACTGCCCC GGACTTGCTC TGCACCTGCT GCAAACCATC 240
AGTCATACAT TTTAGACCAT TTTGAGAAAT CCAAGTTTGT TCCTTTCTTT CCAGGGAAGA 300
ACTTTTTAAG CCAAAAGAAT TATAAATATC CAACTTTCAC TTCGCCTCAC ACAATCAAAG 360
CAGTAAGGAA GTAGCCTCAA AGCAATAAGA AAGGTTCTCT TAAAGGAAAA GGGTTTATTT 420
TATTTTATTT TTTTTTGAGA CGGAGTTTCG CTCTCGTTGC CCAGGCTGGA GCGCAATGGC 480
ACAATCTCAG CTCACTGCAA CCTCCACCTC CTGGGTTCAA GCGATTCTCC TGCCTCAGCC 540
TACCAAGCAG CTGGGATTAC AGGTGCCCAC CACCACACCC GGCTAATTTT TTGTATTTTT 600
AGTAGAAACG GGGTTTCACC ATATTGGCCA GGCTGGTCTC AAACTCCTGA CCTCAGGTGA 660
TCCACCCACC TCGGCCTCCC AAAGTGTTGG GATTACAGGT GTGAGTCACC ATGCCTGGCC 720
AGGAGAGGGT TTCTGCAATG CCTTGGCCCT GCTGGGCTCA GGCAACAGGC CTTTCAAAGT 780
AGGGTTAGTG GGTAGGACAA AGAGAGAGAC AAGCACAGAC AGAAAAATGT CTCATTTTGC 840
TAATGCCCAG TGTAGCACCA TTTCCAGTTT TATTCAGGCA GATGTGCTTA AAACAGCAAA 900
GTAAAACCAC AGTCAGCTCT CAATTATCTG TGAGCTTCAC AGCAGATTTG CAGATTCAAA 960
CAACCACGGA TAGAAACCTG TGGATATAGA ATTCCAACGG TATGACATAA TTTCATATAA 1020
GGGACTTGAG CATCCATGGA TTTTGGTAGT GGTGAGGGTC CTAGAACCAA TCTCCTGTGG 1080
ATAAGAAAGG CTGACTATAC ATATATGTCC TATCGGCTAT TTCTCCTTAC AGTAGAGGAT 1140
ACAGCACCTG TAGACTGGAA CATTTACTCA CTTGCAGACC AGGACATTTA CTCACTGCAT 1200
TTATTCAAGG CCAAGGAATC CCTCTGCCCA AGCTAATTCC AGCTTCACGT CAAGCCTCTA 1260
TGATCACTCT AAGACCCAGA GGCCCATCCT ATGGATTTAG CTCCAGGGAT GCTTTCCCAG 1320
GACCACCCAG AAGCAGCAGA CCAAAAATTC TGTGTTGGAA GGGGAGAATG CTGGGCCACA 1380