EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS129-29871 
Organism
Homo sapiens 
Tissue/cell
MCF10A 
Coordinate
chr5:131793850-131795330 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Klf1MA0493.1chr5:131795063-131795074TGGGTGTGGCC-6.62
Number of super-enhancer constituents: 44             
IDCoordinateTissue/cell
SE_00037chr5:131790656-131796338Adipose_Nuclei
SE_01257chr5:131794641-131795249Adrenal_Gland
SE_09163chr5:131788117-131797621CD14
SE_10340chr5:131790824-131795464CD19_Primary
SE_10915chr5:131787711-131797453CD20
SE_11856chr5:131788689-131797117CD3
SE_13479chr5:131790641-131796411CD34_Primary_RO01536
SE_14495chr5:131789106-131797177CD4_Memory_Primary_7pool
SE_15423chr5:131790548-131794109CD4_Memory_Primary_8pool
SE_16304chr5:131790613-131795606CD4_Naive_Primary_8pool
SE_16894chr5:131794286-131795229CD4p_CD225int_CD127p_Tmem
SE_17370chr5:131789423-131795425CD4p_CD25-_CD45RAp_Naive
SE_17764chr5:131787920-131797394CD4p_CD25-_CD45ROp_Memory
SE_18258chr5:131787905-131797327CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131790791-131797009CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131788439-131797324CD56
SE_20775chr5:131790546-131796689CD8_Memory_7pool
SE_21523chr5:131790963-131794345CD8_Naive_7pool
SE_21960chr5:131790607-131795345CD8_Naive_8pool
SE_22284chr5:131788012-131797561CD8_primiary
SE_23079chr5:131794575-131796517Colon_Crypt_1
SE_23750chr5:131794696-131796088Colon_Crypt_2
SE_25340chr5:131788298-131808279DND41
SE_25784chr5:131790957-131797727Duodenum_Smooth_Muscle
SE_26597chr5:131794257-131796075Esophagus
SE_27629chr5:131790763-131801421Fetal_Intestine
SE_28559chr5:131794264-131804122Fetal_Intestine_Large
SE_30917chr5:131790670-131796844Fetal_Thymus
SE_31393chr5:131794548-131796995Gastric
SE_37771chr5:131791257-131796632HSMMtube
SE_39368chr5:131791092-131797698Jurkat
SE_40726chr5:131794433-131796690Left_Ventricle
SE_42103chr5:131794463-131796999Lung
SE_43869chr5:131790540-131795910MM1S
SE_50023chr5:131791250-131797789RPMI-8402
SE_50051chr5:131790768-131797132Sigmoid_Colon
SE_52336chr5:131790812-131797015Small_Intestine
SE_53285chr5:131790524-131796944Spleen
SE_55171chr5:131794927-131796428Thymus
SE_61818chr5:131790756-131837647Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_65342chr5:131794596-131795860Pancreatic_islets
SE_66244chr5:131791092-131797698Jurkat
SE_67186chr5:131790540-131795910MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5131793909131794808
Number: 1             
IDChromosomeStartEnd
GH05I132452chr5131788089131817782
Enhancer Sequence
GTAAAGCTCA GTGAATTTTC ACAAAATGAA TTTACCCCGA GTAACCAGCA TCCAAATCAT 60
GAAACAGAAC ATCACCAGCA ACCCCTGGTA CCCCTTCCAC TTACTACCTG GCTCCAAAGG 120
CTAATGTCCA TTCTGGCTTC TAATGGTGTA CAGTCATTTC TCCTGTTTTC AAACTTTATA 180
TGATGTAAAT GGAATCAGGC AGTATATATC CTCTTGTTGT GTTTGTGAGA TGATTCATCC 240
AAGTTGTTAC TTAGAGCTGC AGTTTATTCA CTCTTCTTGC TATAGAGTAT TCCACTCTAT 300
GGATATTCCT CGATTTATCC ATTCTACTGT GATGCATTTT TGGATATTCG AGTTGTTATT 360
TATAATTCGG AACTATTCTG ACTATTGCAA TGACATGCTA GTGTGTATTT TTGGAGTACA 420
TGTATATCCA TTGCTGGGGA AGCATGGGTA TGAGTATGTT CAGCTTTAGT ACCTTATGCC 480
AAATAATGTT CCCAGGTGGC TGTACCCATT TACACTCCCT CCAGCAATGT ATGAGAGTTC 540
TGGTTGCTTC ACATTTTTGC CAACCATAGA TATTTTCTAT CTTTTTCATG TTAGCCATTC 600
TGGCAGGTAT GTAGTGGTAT CACAGTGTGG TTTGAATTTG CATTTCCCTG ATGACTAATA 660
CAGCTGAGCA ACCTTTCATA TGTTTGTTAG CCATTTAGAT CTTCTCTTTG CAAAGTGCCT 720
GTTGGAATAT TTGGACATGA GTATTTTTAA AAAGCTCCTT AGGTAACTCT ACTGTGTAGC 780
CAAGGTGGAA AACCACTGAA CTAAAACCAC AAATTAGTAT CTGCGTCTCC CTTTCTTCAT 840
GATTTGCCTT TGAACTTAGA GCATTTTGGA TCTGAGAGGA CCTCGTGGAA CTGGGAAAAG 900
ATTATATTCA CTCCCTACTA AGATGAGCCT GTCAGGAAGA AGCAATTGGA GCTGGCAGTT 960
AAGAATCTTT AGGAATGTGA CCTCTACTTC AGAAGGGTCC AGGGAGGGCC TGTGGTGTCC 1020
ACAGCTGCCA CAGACATTTC CTAACCACAA AAATGGCCCC TTGGTGGTCT CCCCAGAGCT 1080
CCAGGCAGTC ATGGGGAGGA AGCGGAGGGC CCCATGCCAG GTACTTCCCA GTTTCTAGGC 1140
CAACATGAAT GGGACACAGC TCATATGGGG TTGTGGTTAG ACTGGGGACA GTGGAGCATA 1200
TGTTCTGGGG ACCTGGGTGT GGCCAAGGGA GGCCTCCTGT CTGTGGCCTT TGTCCCAGAT 1260
TGGAAATCAG CCAGTGGGGC TCTCCTACAT GGGTCCAGGC CTGGCTAGCT CTTGAATTCT 1320
GTGCGTTTGC ATGTGGGTCC TTATGCATGC GTCCTAGAGC AGGGTCCCAG GGGGCCACTC 1380
CCCCCCCCGA CCCCTTACTC CTCTAAGCTG GGAAACACGT GGCATGAGAG AACACACTGT 1440
GGCTTCTAAT GACATCGTGT CTTGATTGCA TCCCCATTGC 1480