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

HS091-24481

Organism

Homo sapiens

Tissue/cell

HepG2

Coordinate

chr19:49129620-49130940

Target genes

Number: 30
Name	Ensembl ID

CARD8	ENSG00000105483
TMEM143	ENSG00000161558
KDELR1	ENSG00000105438
GRWD1	ENSG00000105447
KCNJ14	ENSG00000182324
CYTH2	ENSG00000105443
LMTK3	ENSG00000142235
SULT2B1	ENSG00000088002
SPACA4	ENSG00000177202
FAM83E	ENSG00000105523
SPHK2	ENSG00000063176
RPL18	ENSG00000063177
DBP	ENSG00000105516
AC008888.7	ENSG00000232871
CA11	ENSG00000063180
NTN5	ENSG00000142233
FUT1	ENSG00000174951
PPP1R15A	ENSG00000087074
NUCB1	ENSG00000104805
CTD	ENSG00000260366
DHDH	ENSG00000104808
BAX	ENSG00000087088
FTL	ENSG00000087086
GYS1	ENSG00000104812
RUVBL2	ENSG00000183207
LHB	ENSG00000104826
CGB	ENSG00000104827
SNRNP70	ENSG00000104852
HRC	ENSG00000130528
AC011450.2	ENSG00000235555

SNPs

Number: 1
ID	Chromosome	Position	Genome Version

rs71335811

chr19

49130071

hg19

TF binding sites/motifs

Number: 2

JASPAR ID

Coordinate

Motif Sequence

Strand

-Log10(p-value)

TBX20	MA0689.1	chr19:49130751-49130762	TTTCACACCTA	-	6.14
TBX2	MA0688.1	chr19:49130751-49130762	TTTCACACCTA	-	6.32

GeneHancer

Number: 1
ID	Chromosome	Start	End

GH19I048626

chr19

49130198

49132145

Enhancer Sequence

TGAGGTGCTG GGCAGCTGCT CTATCCTGGA GCCACCTTGG TGTCTCTGCA GAATTTCCTC 60
CATAGGCAGC TGTGTCTTTA TTTTTCTGTG TGTCTGGGTG ATGTATCTCT CTGGATCCGT 120
TAGGAGTGAT ACACAGGGAT GGGCTACAGA AGGAACAAAA AGACAAGAGG ACCGGATGTG 180
GTGGCTCATG TCTGTAATCC TAGCAATTTG GGAGGCTGAG GCGGGTGGAT CACCTGAGGT 240
CAGGAGTTCG AGACCAGCCT GGCTAACATG GTGAAACCCC ATGTCTACTA AAAATACAAA 300
AAATTAGCCG GGTGTGGTGC TGCGCACCTG TAATCCCAGC TACAGGAGGG TGAGGCAGGA 360
GAATCGCTTG AACCCAGGAG GCAGAGGTTG CAGTGAGCTG AGATCGTGCC ATTGCACTCC 420
AGCTTGGGCA ACAAGAGCAA AACTCTGTCT CCAAAAAAAA AAAAAAAAAA AAAAAAAGCA 480
CAGGCAGAGG TCGCGTGCAG TGGCTCATGC CTATAATCCC AGCACTTTGG GAAGCCAAGG 540
CAGGCAGATC ACCTGAGGTC GGGAGTTCGA GACCAGCCTG GCCAACATGG CGAAACCCTG 600
TCTCTATTAA AAATACAAAA ATTAGCCGGG CATGGTGACG GATGCCTGTA ATTCCAGCTA 660
CTCGGGAGGC TGAGGCAGGA GAATCACTTG AACCCGGGAG GCAGAGGCTG CAGTGAGCCG 720
AGATTGCACC ATTGCACTCC ATCCTGGGCG ACAAGACCGA TACTCCATCA CAAAAAGCAA 780
AACAAAACAA AAACGCAGGC AGAGAAAAGT GATTTACATC TGCTGTTCTC TTGCTAGATT 840
TATGTTTCTG TCTCCTATCC TCTTCCCCTT TGCATGGGTC TTGACCACAG GTGAGTCACC 900
CAGGGTGGTG AGAGCAGCAG CCTGAGACAG GACCAGGTAC CACCCAGAGT GATGGGTGCC 960
AACAGAGGTC TAGGGCTTCC CTGGAGTTCA GAGGTGGCAT CTAATCCTGC CTGGGGCCCC 1020
TAAGGGCTGG AAGTAACCTA ATCCTGGGTA ATAGGTGTTT GGGGTGAGGA AAGTGGGAAC 1080
CACAGCTCTG AACTACAGCT CCTCCCACAC ATGGGGACAA AGGGCATTTG GTTTCACACC 1140
TAAGCCCTGC CTTTGTCTCA GCAGCTAGGA GTTGGGGCAG GGCTGCATAC CTAGGCCTGG 1200
CCACATGAGA GCCAGCAGGT CCCAGGGGCC AGCCCTCCAC CAATTCCGTT GGGGGCTGAT 1260
GAAGGGACTG TTTCCAAGGT GGGGGGCCTG GGTCACTGGC CTCTGCAGAC CCTAACCTCT 1320