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

HS091-32696

Organism

Homo sapiens

Tissue/cell

HepG2

Coordinate

chr22:24896250-24898090

Target genes

Number: 17
Name	Ensembl ID

SPECC1L	ENSG00000100014
UPB1	ENSG00000100024
C22orf45	ENSG00000178803
AP000355.2	ENSG00000228923
SNRPD3	ENSG00000100028
C22orf13	ENSG00000138867
GGT1	ENSG00000100031
FAM211B	ENSG00000178026
AP000356.2	ENSG00000230947
BCRP3	ENSG00000215481
AP000356.1	ENSG00000240906
POM121L10P	ENSG00000224124
AP000357.5	ENSG00000224806
AP000357.4	ENSG00000224334
AP000358.5	ENSG00000237601
AP000358.3	ENSG00000182351
SGSM1	ENSG00000167037

TF binding sites/motifs

Number: 1

JASPAR ID

Coordinate

Motif Sequence

Strand

-Log10(p-value)

ZNF263

MA0528.1

chr22:24896441-24896462

TATTCTGTCTCTCCCTCCTCC

6.14

GeneHancer

Number: 2
ID	Chromosome	Start	End

GH22I024500	chr22	24896581	24896730
GH22I024501	chr22	24897452	24897663

Enhancer Sequence

AGACTCTTTT GACCATAATA AATACACAAA CAGGGTTGTG GCCTGCCCTT GGAGCACACC 60
TGCAGGCCCT GGCTGGCCGC ATACTCCGGG TCTGCAGGCT TGGGCGCCTC AAGCAGTAGC 120
AGAGGCGCTT CTGCCCTGGC CTCCCCACAT CCCTCCAGCC TGCATCTCTG GCTCTTCTGT 180
CTTCCTGTTC TTATTCTGTC TCTCCCTCCT CCTCACTGAT CTTTCCACTT CTCTCCAGCT 240
ATTGATCTGA AGCTCCATTT ACCAACCGGG AGGGTGCCCT TTTGGCCTGC TCGTGCTCTC 300
CACGGGACGC TGCCTCTCAG CTGCCTGCCA GGAGGCGGCC AGCCAGCACA CGCTGGTTGG 360
GACCGTCTGT CCGTGTGTTC TTCTGCCTTA ATCCTCAGGG CGGGGACTCG CTATACCCAG 420
AAGTCTGTCA GTTGTGGTGC CTACAGGATT ACGGGAATAG ATAGGCATTC GCTTATGACC 480
TCAGAGTTAG TAAATAAAGG TGACAGCATC TTGTATCTCC CTAAAGAAAC ATGTTGTCAC 540
AGGCGCAGGT GGTTTGCTTT ATACACTTCT CCACAGCATT CCTCCAGCTG CTCAAACTTT 600
CAGGGATTTT CCTGCACAGG TTTCCTCAGG ATACGGCGTG TTTGAGGATT CTTAGGGATT 660
CTGGAGAAAC CTAAGGCCTC TTGGATTCCA GGTTTGGTTC TGCATCATCA TTCACATTGG 720
TCCTTCCTTT GCTTTTGTTG GATTCACAGA TGTCTGGTTC TCAGTTCTCT CACTTTTTGT 780
ATCAGGATTT GTTTTTTGTG GATATGTCCC CTCTATCATC CCAGACTGTC AAGTCATAGG 840
ACCAGCTATG TTTTTTTCAC GTGCACAGGG CCTAGAAGTA TGCTTTGCGT TTTGCTAACA 900
CCAAGCAAAT GTGTGTTTGC GGGGCTGATG CTGTCAGCAA ATATCCACAA AGCCATGGGG 960
TGCACAGCCT CTCAAAGGAG GAGACTATAG GCCTTGTGGA GAGTTTGTGC GCTCTGGGTT 1020
TTCAGCCTGG TTCCTTTGGT CTGTCTTTGA ACAAACGCTT TTGAATGTCT CCTGGGAGCC 1080
AGGCATTGTG CCAAGGACAA GCAGACAATG AGGATGCTTT CTTCCTATCC CCAAGGAGCC 1140
TGTGGGGTCC TGGGAGTGAC AGACAGCAGA GGAAGAGTGG CACACAAAGC AGTGGCACAC 1200
AATGGCTCCC GAAGGCCAGG GGATGCTGAG TTACCTTGAC ACTTGGCCCA TAGCTGTGAG 1260
AGCCTGCAGA GGCCCACAGA GGGGTGACAT GTGACATAGA TAACACCTCC AGGAAGATTA 1320
GGTGGGAGGA GGGAAGTACA TTCCTGGCCC AGGGCACAGC ACACACCAAA GCACGGGGAT 1380
TTAAAAGAGC CAGAGAGGCG AGGCATTCCA TGATAAGATG CACACAGGAT AAGTAGGATA 1440
AGTGTGGAAC CAGGCTTGCC TCTGAAGGCA GGAGAGTGGG GAGCGGAGTC CCGGGCCAAG 1500
GGGGTGGCTG ACCTGGGAGA TGGGTGTGAA CGTGGGCCCT GGACCGGAAG CAGCACCATC 1560
CTCATCCCTG CCTCTCAGCA ACCCCACAGG TCAGGTGGCA GCCTCCCCAT TACCAGGTGA 1620
GGAAACTGAG GCAGTGTCCA AGTGTCTGAC CCCAGAGCCT CTGCACCTCC AGCTTTTCAT 1680
GCAGATTTTG GACATCAGGA GATAACCAAA TATAGAACCT CCCCACCCTA CTCCTCATAC 1740
CTGCCCAGGT GGGCATTGAT TTTTCCATAT GCATTAGGAT GAGATCCTAA AAATTGCCTT 1800
ACCAATAGAA CTAAATGGAT TCTAATCCTT TTTAAATTCT 1840