EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS192-13725 
Organism
Homo sapiens 
Tissue/cell
U2OS 
Coordinate
chr8:145002160-145003270 
Target genes
Number: 72             
NameEnsembl ID
RP11ENSG00000253971
LY6EENSG00000160932
AK3P2ENSG00000250115
ZFP41ENSG00000181638
GLI4ENSG00000250571
RP13ENSG00000253716
ZNF696ENSG00000185730
TOP1MTENSG00000184428
C8orf51ENSG00000254389
RHPN1ENSG00000158106
MAFAENSG00000182759
ZC3H3ENSG00000014164
7SKENSG00000221399
GSDMDENSG00000104518
C8orf73ENSG00000204839
NAPRT1ENSG00000147813
TIGD5ENSG00000179886
EEF1DENSG00000104529
PYCRLENSG00000104524
TSTA3ENSG00000104522
ZNF623ENSG00000183309
ZNF707ENSG00000181135
CCDC166ENSG00000255181
MAPK15ENSG00000181085
FAM83HENSG00000180921
MIR937ENSG00000216090
SCRIBENSG00000180900
PUF60ENSG00000179950
NRBP2ENSG00000185189
EPPK1ENSG00000227184
PLECENSG00000178209
GRINAENSG00000178719
SPATC1ENSG00000186583
PARP10ENSG00000178685
CTDENSG00000204791
OPLAHENSG00000178814
EXOSC4ENSG00000178896
GPAA1ENSG00000197858
CYC1ENSG00000179091
MAF1ENSG00000179632
KIAA1875ENSG00000179698
SHARPINENSG00000179526
FAM203AENSG00000235173
TSSK5P1ENSG00000227473
HEATR7AENSG00000179832
SCXBENSG00000187786
AC145291.1ENSG00000204775
FAM203BENSG00000230567
BOP1ENSG00000170727
HSF1ENSG00000185122
GS1ENSG00000254690
DGAT1ENSG00000185000
SLC52A2ENSG00000185803
FBXL6ENSG00000182325
ADCK5ENSG00000173137
CPSF1ENSG00000071894
SLC39A4ENSG00000147804
VPS28ENSG00000160948
AC084125.4ENSG00000232600
TONSLENSG00000160949
CYHR1ENSG00000187954
KIFC2ENSG00000167702
PPP1R16AENSG00000160972
GPTENSG00000167701
MFSD3ENSG00000167700
RECQL4ENSG00000160957
LRRC14ENSG00000160959
LRRC24ENSG00000254402
C8orf82ENSG00000213563
AC084125.1ENSG00000255681
AC084125.2ENSG00000256822
ZNF251ENSG00000198169
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_09260chr8:145001615-145004223CD14
SE_10783chr8:145002022-145002657CD19_Primary
SE_10783chr8:145002700-145003861CD19_Primary
SE_11513chr8:145000243-145019270CD20
SE_12121chr8:145001820-145003740CD3
SE_14847chr8:145001877-145003787CD4_Memory_Primary_7pool
SE_16928chr8:145002006-145002705CD4p_CD225int_CD127p_Tmem
SE_16928chr8:145002783-145003628CD4p_CD225int_CD127p_Tmem
SE_17383chr8:145001489-145006178CD4p_CD25-_CD45RAp_Naive
SE_17884chr8:145001416-145005728CD4p_CD25-_CD45ROp_Memory
SE_19196chr8:145002701-145003757CD4p_CD25-_Il17p_PMAstim_Th17
SE_21381chr8:145001786-145003999CD8_Memory_7pool
SE_23034chr8:145001784-145003812CD8_primiary
SE_23735chr8:145002145-145002599Colon_Crypt_2
SE_23735chr8:145002822-145003249Colon_Crypt_2
SE_29600chr8:145001695-145002653Fetal_Muscle
SE_31395chr8:145002207-145002745Gastric
SE_31395chr8:145002786-145003438Gastric
SE_34673chr8:145001777-145003776HeLa
SE_48066chr8:145001449-145002688Psoas_Muscle
SE_50057chr8:145001913-145002680Sigmoid_Colon
SE_50057chr8:145002744-145004471Sigmoid_Colon
SE_52367chr8:145001947-145002665Small_Intestine
SE_52367chr8:145002691-145003679Small_Intestine
SE_55146chr8:145001849-145002621Thymus
SE_55146chr8:145002788-145004963Thymus
SE_61753chr8:145002108-145053930Toledo
SE_62528chr8:145001740-145054046Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr8145002494145002937
chr8145002487145003186
Enhancer Sequence
CTGGCGGGAA AGCGGGGCTC AGGGCCATGA CATGGGGCTC GAGCAATAGC CCAAGGGAAT 60
GGAACCCAAG CCACAGCGAC CCAGGGTGCT GCCTGCCAAG CCCAGACCCA ACCCTGGGGG 120
TCAGCTGACC CTGTGGTCAG AGGCTTGCTT CAGGAGAAGA ACAGCCTTGG GGAGAAGGAG 180
GTTGGGAGCC TCTGTAACAC AAGGACACTC AGGACCCAGC CTGGAGAGGG GGTGCGCCAG 240
CCAGGAACGG CAGACCCCAA GGCCCCGAGA CAGGACGAGC CCACTGGCTG GATGACAGCG 300
GCATCCTGGT GCCCACAGGG CCTGGAAGCG TAGTTCTCAG CCCTTGCAGC CCAAGACTGG 360
GCGAAGGGGA CACCGGGGTG GAAATGGCAC CCTGTGGTAG CCAGCGGCGG CCCTATCACT 420
GTGCTGGTTC TGTGAGGAGT AGACAGCGGG TGGACCTGTG GTTTGCAACA CAGGAAGAGG 480
CGGCGGCCCT ATCACTGTGC TGGTTCTGTG AGGAGTAGAC AGCGGGTGGA CCTGTGGTTT 540
GCAACACAGG AAGAGGTGGC GGCCCTATCA CTGTGCTGGT TCTGTGAGGA GTAGACAGCG 600
GGTGGACCTG TGGTTTGCAA CACAGGAAGA GGCGGCGGCC CTATCACTGT GCTGGTTCTG 660
TGAGGAGTAG ACAGCGGGTG GACCTGTGGT TTGCAACACA GGAAGAGACT ATGACATAAC 720
ACATTGGAAA TAAATGCCAG AGGCCCTTAA GTCCAGGCCA GGAACAGGAC AGACGAGAGG 780
CAGGGTGCAG GATTCCTTAC TGTGCCACTG AAAGTGGATC CACAGCTTCC CCACCTCACT 840
CAGCAGCCGC TGCCCAGCTC CACTGTCTCT TCCCCACACC CGAATCTCAT CACCAGGAAG 900
TCCCCCGGCC GCCACTGTCG AAGCGTATCC AGCCCTGAAC TCTTCTCACC ACCTCTGCGG 960
CCACCACCCC AGCTGGGCCT CCCGCCTCCT GGCCAGATCT CTGAACAGCC CCCAACTCGT 1020
TCCCTCCTGC ACCCTCCTGC AAGGTCACAG CCCTCACCCC AGCACCCCCC AGCCGACCCC 1080
AGCCCCTCGC CTGTGGCCAG GTGCACTCAC 1110