EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS129-36651 
Organism
Homo sapiens 
Tissue/cell
MCF10A 
Coordinate
chr8:145010180-145011140 
Target genes
Number: 55             
NameEnsembl ID
RP11ENSG00000253971
AK3P2ENSG00000250115
ZFP41ENSG00000181638
GLI4ENSG00000250571
RP13ENSG00000253716
ZNF696ENSG00000185730
TOP1MTENSG00000184428
C8orf51ENSG00000254389
RHPN1ENSG00000158106
MAFAENSG00000182759
ZC3H3ENSG00000014164
7SKENSG00000221399
GSDMDENSG00000104518
C8orf73ENSG00000204839
NAPRT1ENSG00000147813
TIGD5ENSG00000179886
EEF1DENSG00000104529
PYCRLENSG00000104524
TSTA3ENSG00000104522
ZNF623ENSG00000183309
ZNF707ENSG00000181135
CCDC166ENSG00000255181
MAPK15ENSG00000181085
FAM83HENSG00000180921
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
CPSF1ENSG00000071894
SLC39A4ENSG00000147804
VPS28ENSG00000160948
Number of super-enhancer constituents: 44             
IDCoordinateTissue/cell
SE_01079chr8:145009954-145021718Adrenal_Gland
SE_02411chr8:145010061-145011686Astrocytes
SE_02906chr8:145009852-145010708Bladder
SE_02906chr8:145010761-145012497Bladder
SE_09260chr8:145007117-145019257CD14
SE_11513chr8:145000243-145019270CD20
SE_12121chr8:145010181-145011691CD3
SE_14847chr8:145010362-145018605CD4_Memory_Primary_7pool
SE_16928chr8:145010521-145018475CD4p_CD225int_CD127p_Tmem
SE_17383chr8:145006613-145020039CD4p_CD25-_CD45RAp_Naive
SE_17884chr8:145006516-145019331CD4p_CD25-_CD45ROp_Memory
SE_18961chr8:145009606-145018737CD4p_CD25-_Il17-_PMAstim_Th
SE_19196chr8:145007074-145018699CD4p_CD25-_Il17p_PMAstim_Th17
SE_23089chr8:145007443-145021710Colon_Crypt_1
SE_23735chr8:145010020-145019304Colon_Crypt_2
SE_24704chr8:145005616-145021714Colon_Crypt_3
SE_26583chr8:145007009-145030049Esophagus
SE_31395chr8:145007455-145021754Gastric
SE_34239chr8:145003594-145029511HCT-116
SE_34673chr8:145007097-145028424HeLa
SE_36390chr8:145009631-145016286HMEC
SE_37176chr8:145007038-145028465HSMMtube
SE_38740chr8:145009678-145019138HUVEC
SE_39050chr8:145009925-145011789IMR90
SE_40656chr8:145009499-145021778Left_Ventricle
SE_42376chr8:145006289-145021766Lung
SE_44278chr8:145009784-145020889NHDF-Ad
SE_44786chr8:145009947-145012076NHLF
SE_46253chr8:145009702-145019036Osteoblasts
SE_47321chr8:145008032-145032287Panc1
SE_47503chr8:145010086-145010566Pancreas
SE_48066chr8:145006204-145021794Psoas_Muscle
SE_50057chr8:145007167-145021759Sigmoid_Colon
SE_51144chr8:145006191-145029766Skeletal_Muscle
SE_52367chr8:145009989-145020005Small_Intestine
SE_53601chr8:145006717-145021756Spleen
SE_55146chr8:145010667-145011134Thymus
SE_56139chr8:145009456-145011870u87
SE_56852chr8:145005920-145021728VACO_400
SE_57360chr8:145009497-145010847VACO_503
SE_57360chr8:145010915-145018935VACO_503
SE_61753chr8:145002108-145053930Toledo
SE_62528chr8:145001740-145054046Tonsil
SE_67795chr8:145009456-145011870u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr8145010400145011000
Enhancer Sequence
ATCTGCTCAC AGCAGAGAGG AGGCCACAGC TCAGCCACAG CCACCAGGCC TGCTCTGTGC 60
CCACAGCCAC ATGCACAGGG GCAGGGGTAG CTCAGCACCC AGGGGGAGTG CATGGGGCCA 120
CCAAACCAGC CAGGGCAGCA CCGGGCTCCA GGGCCCTTCC CTGTTGGGAA GCTGCTGGGA 180
CTGGCCATGC CTCGGGGCCA CAAGTCCAGC CACTCCAGCC GGTGGCAGCT GCCACCACGC 240
AGCTCAGAAC CCCCAACCCT CACTGCCACC ACACAGCAGG TGCCCACTCC CCTAGCTGGG 300
GAGGGCTAGG CTGCACCCTG CACCTCCCGG AGCTGGGATG GAGCAGAGTG GAAGGGCAGT 360
GGGCATAAGA GGAACCCACA AGTGTACCAC TAAACCTGGC CCAGAACCCC CAGGCCTGGA 420
AAAGGCTGGG GGTCGAGCTC CATCGATGGT TGCAGGCTGG CAGGTGGGGC CTCTGGCAGC 480
CTGGCTTTAC ACTCAGTGGC ATGCTCAGGC CAGGTTCTGC CCACCCACCC CTAGCTGCCT 540
GTCGTCCTGC CAGCCTGTGT GACTCAGCTG CCGTGCCAGC ACCAGGCTCT GCCTGCTCAG 600
CTCTCAGATT TGTGGTTTCC TGTGCAGCCA GGACAAGCAG CGGGTGAGTC AGCCTGTGCT 660
GCGCAGAAGC CTCCCCAGGG CAGGCACCGG GGCCTGCATT CCTCCACAGG GAGGCTCTGG 720
GCCCTGCCCA GCCAGGGCCA GAGGGCACGG ATAGGTGGCC TCAGAGAGAG GCCTGTACCC 780
TCAGGCCACA GATCCAGTCC AGGGTTGCGG CTGGCAGGAA GGCACCCAGG TGCCACCATA 840
CCTACGGCGC CAGTCACCTC CCAGGCCACG CCCTAGCCAG AAAGCGGATC AACCCGCCAG 900
CCAAGGAGCC CAGGCTACCC TGGAAACTCC TGCAGGGGGT GGGGGTCCTG GGGGCAGCCG 960