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

TagContent
EnhancerAtlas ID
HS101-09593 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr12:6344730-6345350 
Target genes
Number: 46             
NameEnsembl ID
CD9ENSG00000010278
RP1ENSG00000256103
PLEKHG6ENSG00000008323
TNFRSF1AENSG00000067182
LTBRENSG00000111321
SCNN1AENSG00000111319
CD27ENSG00000139193
LOC678655ENSG00000215039
TAPBPLENSG00000139192
VAMP1ENSG00000139190
NCAPD2ENSG00000010292
MRPL51ENSG00000111639
SCARNA10ENSG00000239002
RP5ENSG00000255966
GAPDHENSG00000111640
IFFO1ENSG00000010295
NOP2ENSG00000111641
SCARNA11ENSG00000247853
CHD4ENSG00000111642
LPAR5ENSG00000184574
ING4ENSG00000111653
ZNF384ENSG00000126746
C12orf53ENSG00000139200
COPS7AENSG00000111652
PTMSENSG00000159335
MLF2ENSG00000089693
LAG3ENSG00000089692
CD4ENSG00000010610
LEPREL2ENSG00000110811
GNB3ENSG00000111664
CDCA3ENSG00000111665
USP5ENSG00000111667
TPI1ENSG00000111669
RPL13P5ENSG00000240370
DSTNP2ENSG00000248593
SPSB2ENSG00000111671
ENO2ENSG00000111674
ATN1ENSG00000111676
PTPN6ENSG00000111679
U47924.27ENSG00000257084
LPCAT3ENSG00000111684
ABC12ENSG00000205885
C1RLENSG00000139178
RBP5ENSG00000139194
CLSTN3ENSG00000139182
RP11ENSG00000256967
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXA1MA0148.4chr12:6344888-6344904CTCTGTTTACTCAAGG-6.23
Sox3MA0514.1chr12:6344909-6344919AAAACAAAGG-6.02
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_00985chr12:6344038-6345660Adrenal_Gland
SE_02955chr12:6345063-6345485Bladder
SE_03308chr12:6337700-6345175Brain_Angular_Gyrus
SE_03988chr12:6336456-6345847Brain_Anterior_Caudate
SE_04905chr12:6328630-6346354Brain_Cingulate_Gyrus
SE_05857chr12:6328573-6346408Brain_Hippocampus_Middle
SE_06790chr12:6328750-6346091Brain_Hippocampus_Middle_150
SE_07876chr12:6328735-6347463Brain_Inferior_Temporal_Lobe
SE_23086chr12:6344001-6345944Colon_Crypt_1
SE_23760chr12:6344109-6344912Colon_Crypt_2
SE_23760chr12:6344913-6345648Colon_Crypt_2
SE_24754chr12:6343867-6345992Colon_Crypt_3
SE_25881chr12:6332674-6346002Duodenum_Smooth_Muscle
SE_26531chr12:6343650-6346116Esophagus
SE_27879chr12:6343571-6345671Fetal_Intestine
SE_28805chr12:6330455-6345849Fetal_Intestine_Large
SE_31631chr12:6344094-6345036Gastric
SE_33937chr12:6343484-6344929HCC1954
SE_33937chr12:6344952-6345636HCC1954
SE_37830chr12:6337296-6345407HSMMtube
SE_41591chr12:6344060-6346257LNCaP
SE_42122chr12:6344045-6346105Lung
SE_50072chr12:6336509-6346097Sigmoid_Colon
SE_52457chr12:6336504-6345611Small_Intestine
SE_53862chr12:6343875-6345556Spleen
SE_54512chr12:6320070-6346293Stomach_Smooth_Muscle
SE_57134chr12:6344070-6344831VACO_400
SE_57134chr12:6344914-6345472VACO_400
Number: 1             
IDChromosomeStartEnd
GH12I006213chr1263222806345639
Enhancer Sequence
GGTAAACTCA GACCAGGATC CTGGTGTCCC TGCCCCCATT GCTCTGGACA AACCCTGCAA 60
GCATGAAAGT GACAGCAGCC AAGTGCTGCT TCAGCAAGAC CCGTTCTGCC TGTGAAAGGG 120
CCCCAGGGCA CCCATCTCTT TCTCTCCCAC TTTGGGCCCT CTGTTTACTC AAGGGCAATA 180
AAACAAAGGC CGGACCAGGG GAATGACAAG TGTTCTGGCA CCGCCCACTG CTGCCAGCCC 240
GGAAGCTCTC AAGGGCAGGC GTGCTTCTGA GTCTTGGACT CCCACTCTGA CTTTGTCAGT 300
GGCTCCTGTC TGTAAGCCAG AGTTAATGTC CAACTCCAGA ATAGTAAAAG GTGACCTTAC 360
AACCATGTCA GAAATAGACC CCCAAGCAGG GCCTGTCCCT CCTCCTTCCC TGACGTCCTG 420
CCCAGATTTT AGGGATCCAC TAGCATAGCC ATCCCTTTGT TCCCCTTTCC ATCCACCAGC 480
CAGAACTTCT CTTATCCCCG AACACTCCTG TCCCCAGCCC ACCCTCTGCC CACCAGTTCT 540
CCCGGGTGAG ACGGGGGCCA TGGGAGGGAG GAGGTGCCCT GGGAGGAAGG ATTGTGTGTG 600
ACCCAGGTCT TGGTTTGTCT 620