EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS190-00107 
Organism
Homo sapiens 
Tissue/cell
Treg_cell 
Coordinate
chr1:12210210-12211660 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr1:12211538-12211559ACCTCATCTTTCTCCTCCTCC-7.23
ZNF263MA0528.1chr1:12211541-12211562TCATCTTTCTCCTCCTCCTCC-8.2
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_00369chr1:12202440-12211059Adipose_Nuclei
SE_04546chr1:12209905-12211237Brain_Anterior_Caudate
SE_06521chr1:12209695-12211557Brain_Hippocampus_Middle
SE_09154chr1:12199965-12214486CD14
SE_10696chr1:12207898-12214373CD19_Primary
SE_11902chr1:12208865-12214231CD3
SE_14553chr1:12208809-12214332CD4_Memory_Primary_7pool
SE_15480chr1:12208768-12214030CD4_Memory_Primary_8pool
SE_16369chr1:12209491-12212458CD4_Naive_Primary_8pool
SE_16946chr1:12210087-12214122CD4p_CD225int_CD127p_Tmem
SE_17650chr1:12208923-12214185CD4p_CD25-_CD45RAp_Naive
SE_17827chr1:12206501-12214454CD4p_CD25-_CD45ROp_Memory
SE_18389chr1:12206868-12214379CD4p_CD25-_Il17-_PMAstim_Th
SE_19117chr1:12208827-12214340CD4p_CD25-_Il17p_PMAstim_Th17
SE_20048chr1:12207907-12214477CD56
SE_20873chr1:12208284-12214108CD8_Memory_7pool
SE_22347chr1:12207903-12214404CD8_primiary
SE_26251chr1:12206411-12213727Duodenum_Smooth_Muscle
SE_27503chr1:12209763-12212109Esophagus
SE_30788chr1:12209786-12211445Fetal_Muscle
SE_32030chr1:12209823-12210827Gastric
SE_32030chr1:12210903-12211697Gastric
SE_41498chr1:12209754-12211519Left_Ventricle
SE_42336chr1:12209781-12214078Lung
SE_48967chr1:12209749-12211554Right_Atrium
SE_50250chr1:12207958-12214180Sigmoid_Colon
SE_52522chr1:12206320-12214007Small_Intestine
SE_53313chr1:12206186-12214442Spleen
SE_55394chr1:12209790-12211650Thymus
SE_59216chr1:12197780-12224862Ly3
SE_61096chr1:12184746-12245090HBL1
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11221043012211346
Number: 1             
IDChromosomeStartEnd
GH01I012140chr11220016112214656
Enhancer Sequence
AGATCTTATG TGTCAGCAGG AGCACTTCAC ATACTGTCTC ATTTTAGCCT CTCGGTAATT 60
TTGCCATTAT TGTCCTTGGA GTTGGCTCAA GGAAGCTACA TAACCTGGTG GAATCCCAAG 120
TTCCTCTGGC TGGAATTTGG ATCCAAGCTG GTCTGTCTCC AGAGTGTGAG CTCTGGACTG 180
AGCAGCTGAC CTGTGCATTC AGGGACCCAT ACAGTCAGAA TGTGGCAGGA CTGGAAAGCA 240
AGCTCACATC TGTCTGATTA GAGAACATCT GAGCTTGGTA CCCATACAAA CTAGGCCCTA 300
TCTAGTTTTT AGATAGGGAA ATCAAGGCTC TGAGAGGTCT TGCCAGGCCT CTCCTGAGGA 360
AGAGGGCAGG GTCTGGGACC TTCCAGGGCA GGATGGGGCC CCCAACTTGG GTTGCACAGA 420
ACCATGTCAG GAAGTCACAT AGAGTTGTGG GTAGATTATG CAAGTACAGG CTGTCAGGAG 480
GGATGTTGTT TTTCACTGCA ATTACACTTC ACTCAGGAAA TACAGCTTCT GCACGTACTG 540
AGGGAGGGTT CCTCACCCTG TGCAGAAGAC CTCCTGGTGA ATACCGGGGC ACTCGCTGGG 600
TGACCCTGGG TCCTCTGGGC CAAGTTCATG CATCGAAAGT TCCCTGAGAA GCTCTTTGTG 660
CCCATCTGGG TTGGGCTTTG ACAATAGAGT TGAAGAGGCT TTATTCCTGC CATGCATGGA 720
GTCACAGGTT AGTAAGAAAG ATGATAAGAG CTGTACTTGA GGCTTTCGTG TGCTCTCACT 780
TAAACCTCAC AGTGCACTAG GAAGTAGTTA TTACATTACC CCTATGTTAC AGATGAGGAA 840
ACCAACACGC AGAGTGGCTA AGCCAGTTCC CCAGGGTCAC ACAGCTGCTA AGTGGCGCAG 900
CTAGGCTTTG AACCCAGGCC ACCTGGCTGG AGTCTGCGTC CTCACACACT TGGCCATGCT 960
GCTCCATTGT GGCTCAGGCC GAGGTCACCA CTGTGCTGAG GCCCCAGCCC TGAGTCCCAG 1020
ACCCTGTAGA ACACTGTGCA GGCATCCATG GGGCTCAGTG AATGCACAGG GAATGGAATT 1080
TGCTCTTGGT TTTTATCCCA CCTTTCCTTT CCAAAGCCCA GCTGTGGCCA GGCCTCTCCC 1140
TCACAGAACC TTCTATGACT CCCTAGTGCC TACATGCCAA TGTCTGCCAA TCCAGCTTTG 1200
CTGCTACCTC CACAGCTCCC ATATCTAAAC CTCTCCTGAG ACCCGACTGT TTCCGCTCAG 1260
TCACCAAATA CAGAGGGCAT ATCCTCATCA TGAAATCTCT GCTCAGCGCT CCAACCCCTG 1320
AATTTCCAAC CTCATCTTTC TCCTCCTCCT CCAAAAACCC TTCCAGGACA CCCAGGCCCA 1380
GGACCTCCAA GCTCCCACAG CACTGACTGT GAAGGGGGAC TGGAGGCCAA GTTCTAGAAG 1440
TCTTGCAAAA 1450